An observational study in Crohn Disease, Ulcerative Colitis and Pouchitis, sponsored by Eli Sprecher, MD. Status unknown at 1 site in Israel. Open to participants aged 18 Years to 80 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-10-13.
Sponsored by Eli Sprecher, MD · Observational
The inflammatory bowel diseases (IBDs), ulcerative colitis (UC) and Crohn's disease (CD), are characterized by lifelong relapsing-remitting gastrointestinal inflammation, with symptoms of abdominal pain, diarrhea, and rectal bleeding during active disease. Medical therapy reduces intestinal inflammation and ameliorates symptoms. Medical cannabis has recently been added to the arsenal of symptom-reducing measures in IBD. Though the efficacy of THC and CBD have been established as the two most dominant ingredients of cannabis, the rest of the plant phytochemicals are unknown, and effects on patients are not yet determined.
Hypothesis (es) and Aims:
Prospectively follow IBD patients receiving medical cannabis as treatment of their disease (group 1) in comparison to the following control groups:
To analyze the optimal drug level for disease management in various IBD patient types.
Study design:
Eligible IBD patients treated at the IBD clinic in the Tel Aviv Medical Center participating in the study, which have signed an informed consent form and answered to all the study inclusion criteria. Patients will be informed of the study by their treating physician, recruited and followed throughout the follow-up period by study coordinators.
This study will include five patient groups:
Group 5 (Cannabis responders group): up to 100 IBD patients previously prescribed cannabis and were identified to have positive effect on their disease
*Study plan:
At baseline, demographic characteristics, medical history, concomitant medication assessment, disease related therapy and failed therapy will be documented.
Study visits:
Among the study group: recruitment at time 0, after one month (±14 days) of treatment, at three months (±21 days) and at 6 months (±30 days) of therapy (end of study), will be conducted, in which patients will be asked to fill in questionnaires, give biologic samples, undergo clinical, anthropometric and nutritional evaluation and physician assessment and monitoring of therapy, safety and adverse events. The cannabis producing company, composition, quantity and way of consumption will be documented.
•Among control group and Cannabis responders group: Healthy controls will be samples once at baseline. All IBD control groups (groups 3-5) will be followed up similarly as the study group and will undergo all sampling and questionnaires, at times 0, 3, 6 months (excluding the 1 month cannabis dose adjustment meeting).
Patients will be asked to inform in case of relapse during the follow up period and provide stool and blood samples before therapy is changed. At relapse time point, disease activity index will be recorded and questionnaires will be completed.
*Sample collection: Baseline and follow up study visits will include biologic samples collection (blood, feces) from which blood levels of complete blood count (CBC), Albumin, Liver enzymes (ALT, AST, ALP), lipid panel (Total cholesterol, LDL, HDL, triglycerides), creatinine, fasting glucose, C-reactive protein (CRP), drug levels and antibodies (for patients treated with thiopurines and biologics), and fecal levels of Calprotectin will be measured.
White blood cells will be separated and stored for m RNA analysis of cannabinoid metabolism. Only RNA fractions will be extracted and analyzed, no DNA will be assessed and no genetic sequencing will be performed . In addition, 10 ml of blood will be drawn for analysis of Th17 cells. CD4 T cells will be purified from peripheral blood of IBD patients by RosetteSep™ Human CD4+ T Cell Enrichment Cocktail kit. STAT3 and IL-17 levels will be analyzed. The samples analysis will be done at Dedi Meiri's lab at the Technion-IIT. Serum, and fecal samples will be stored at -80◦C for future analysis after being authorized by the IRB and by law including cannabis phytochemical analysis (10ml of each) on WBC and on biopsies when available and for fecal microbiome analysis. In appendix A- a detailed list of all tests in each visit.
*Endoscopic evaluation: In patients who will undergo a standard of care endoscopic examination for clinical reasons: these will include mucosal and histologic assessment for disease severity (SES-CD and MAYO score for CD and UC patients respectively, PDAI for Pouchitis patients).
Mucosal biopsies will be collected from inflamed and healthy areas, and from standard areas of the GI track (table 1), sent for histology assessment and stored for future analysis after being authorized by the IRB and by law. These samples will be stored in RNA Later snapped frozen and stored at -80◦c until analysis. No more than 10 samples will be collected during endoscopy including samples for clinical assessment. Samples from recto-sigmoid junction (20 cm from anus) will be taken in every colonoscopy, regardless of the status of inflammation.
*Biologic sample handling: Samples will be stored at -80◦c while coded with no identifying information; access to samples will be restricted to the study staff only. Samples will be stored up to 10 years from final data collection.
In this study, serum and fecal samples analyzed will include those gathered from protocol number 0276-19 and from protocol number 0250-17 in patients using medical cannabis only. In the later group, samples will be used only if the patient had agreed for use of samples in other studies other than 0250-17. To both studies, Professor Nitsan Maharshak is PI.
*Questionnaires:
Baseline and follow up study visits will include data collection from the following:
Anthropometric and nutritional evaluation:
Nutritional status will be evaluated by a MUST questionnaire
*Study endpoints: the study will follow patients throughout 6 months of treatment and follow disease remission (clinical/biochemical) or exacerbation.
Disease remission:
Disease exacerbation:
Medical treatment change by treating physician
Statistical analyses will be performed using SPSS version 23.0 for Windows. Patients who adhere to the study's protocol (defined as preforming ≥ 80% of exercises) will be included in data analysis. An intention-to-treat analysis will include patients excluded because of non-adherence to the intervention.
Descriptive statistics will be used to describe the distribution of variables associated with characteristics of the study sample. Continuous variables will be presented as means± SD and dichotomous/categorical variables as proportions. The normality of the distribution of continuous variables will be tested by the Kolmogorov-Smirnov test. If normality is rejected, non-parametric tests will be used.
Univariate analysis: To test the association between continuous variables with normal distribution, the Pearson correlation coefficient will be performed. To test associations between continuous variables which do not distribute normally or for ordinal variable, the spearman correlation coefficient will be used. To test differences in continuous variables between the treatments arms the t-test for independent groups (or Mann-Whitney test for non-normally distributed variables) will be performed. For comparison of dichotomous or categorical variables the Chi-square test will be performed.
To compare baseline to end of treatment parameters within arms for continuous variables the t-test for dependent groups will be performed (or Wilcoxson test for non-normally distributed variables), in dichotomous/categorical variables the McNemar Test will be performed.
To test differences in continuous variables between the treatment groups in numbers of time points the Mix model for repeated measures will be performed. To test differences in dichotomous/categorical variables between the treatment groups in numbers of time points Generalized estimating equation will be performed.
1,992 studies on the registry are indexed under Crohn Disease; 478 are open to participants now.
This study's planned enrollment of 1,000 is above the median of 185 across 645 observational studies indexed under Crohn Disease.
Browse Crohn Disease studies →Eli Sprecher, MD is the lead sponsor of 5 studies on the registry; 1 is open to participants now.
Counted across the registry records on this site, refreshed daily.
Study population:
Eligible IBD patients treated at the IBD clinic in the Tel Aviv Medical Center participating in the study, which have signed an informed consent form and answered to all the study inclusion criteria. Patients will be informed of the study by their treating physician, recruited and followed throughout the follow-up period by study co-ordinators.
This study will include five patient groups:
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Patients (male and female, age 18-80 years) diagnosed with Crohn's disease (CD), ulcerative colitis (UC) or pouchitis, and healthy volunteers.
All patients will sign an form. IBD patients who are recruited to group 3 will be included if they report mild-severe abdominal pain in clinical questioning of clinical activity (Harvey-Bradshaw index).
Healthy participants recruited to group 2 will be healthy volunteers with no prior/current use of medical cannabis
Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
IBD patients prescribed cannabis as treatment of their bowel disease.
Drug: Medical Cannabis
One hundred healthy patients who do not use cannabis and are not eligible or not interested to commence this intervention.
Up to 100 IBD patient who experience pain and do not use cannabis
Up to 100 IBD patient who do not experience pain and do not use cannabis
up to 100 IBD patients previously prescribed cannabis and were identified to have positive effect on their disease
Patients will be observed throughout their treatment with medical cannabis, prescribed to them by for clinically treating their disease (treatment is not an intervention of the study).
Determine patients clinical response rates using Harvey-Bradshaw Index (HBI) in Crohn's disease patients receiving cannabis at week 4
Disease clinical response will be measured as the change in HBI scores from baseline to week 4. A clinical response is defined as reduction of at least 3 points in HBI score, ∆HBI\>3 in patients with baseline HBI\>7. Harvey-Bradshaw Index (HBI) is a tool for assessing the degree of illness (activity) in patient's with Crohn's disease. Higher score means higher disease activity and severity. A drop \> 3 is considered a clinical response.
Time frame: week 4
Determine the clinical response rates using SCCAI (Simple Clinical Colitis Activity Index) in patients with Ulcerative Colitis receiving cannabis at week 4
Disease clinical response will be measured as the change in SCCAI scores from baseline to week 4. A clinical response is defined as reduction of at list 30% in SCCAI score, ∆SCCAI\>30% for Ulcerative Colitis SCCAI (Simple Clinical Colitis Activity Index) is used to assess the severity of symptoms in people who suffer from ulcerative colitis. Score range from 0 to 19 points 0\<SCCAI\<19. Higher score means higher disease activity and severity.
Time frame: week 4
Determine patients clinical response rates using Harvey-Bradshaw Index (HBI) in Crohn's disease patients receiving cannabis at week 12
Disease clinical response will be measured as the change in HBI scores from baseline to week 12. A clinical response is defined as reduction of at least 3 points in HBI score, ∆HBI\>3 in patients with baseline HBI\>7. Harvey-Bradshaw Index (HBI) is a tool for assessing the degree of illness (activity) in patient's with Crohn's disease. Higher score means higher disease activity and severity. A drop \> 3 is considered a clinical response.
Time frame: week 12
Determine the clinical response rates using SCCAI (Simple Clinical Colitis Activity Index) in patients with Ulcerative Colitis receiving cannabis at week 12
Disease clinical response will be measured as the change in SCCAI scores from baseline to week 12. A clinical response is defined as reduction of at list 30% in SCCAI score, ∆SCCAI\>30% for Ulcerative Colitis SCCAI (Simple Clinical Colitis Activity Index) is used to assess the severity of symptoms in people who suffer from ulcerative colitis. Score range from 0 to 19 points 0\<SCCAI\<19. Higher score means higher disease activity and severity.
Time frame: week 12
Determine patients clinical response rates using Harvey-Bradshaw Index (HBI) in Crohn's disease patients receiving cannabis at week 24
Disease clinical response will be measured as the change in HBI scores from baseline to week 24. A clinical response is defined as reduction of at least 3 points in HBI score, ∆HBI\>3 in patients with baseline HBI\>7. Harvey-Bradshaw Index (HBI) is a tool for assessing the degree of illness (activity) in patient's with Crohn's disease. Higher score means higher disease activity and severity. A drop \> 3 is considered a clinical response.
Time frame: Week 24
Determine the clinical response rates using SCCAI (Simple Clinical Colitis Activity Index) in patients with Ulcerative Colitis receiving cannabis at week 24
Disease clinical response will be measured as the change in SCCAI scores from baseline to week 24. A clinical response is defined as reduction of at list 30% in SCCAI score, ∆SCCAI\>30% for Ulcerative Colitis SCCAI (Simple Clinical Colitis Activity Index) is used to assess the severity of symptoms in people who suffer from ulcerative colitis. Score range from 0 to 19 points 0\<SCCAI\<19. Higher score means higher disease activity and severity.
Time frame: Week 24
Determine clinical remission rates using Harvey-Bradshaw Index (HBI) in Crohn's disease patients receiving cannabis at weeks 4
Disease remission will be defined by HBI \<5 Higher HBI clinical score means higher disease severity: Remission\<5 Mild Disease 5-7 Moderate Disease 8-16 Severe Disease \>16
Time frame: week 4
Determine clinical remission rates using SCCAI (Simple Clinical Colitis Activity Index) in patients with Ulcerative Colitis receiving cannabis at week 4
Disease remission will be defined by SCCAI \<3 SCCAI (Simple Clinical Colitis Activity Index) score range from 0 to 19. Higher score means higher disease severity.
Time frame: week 4
Determine clinical remission rates using Harvey-Bradshaw Index (HBI) in Crohn's disease patients receiving cannabis at weeks 12
Disease remission will be defined by HBI \<5 Higher HBI clinical score means higher disease severity: Remission\<5 Mild Disease 5-7 Moderate Disease 8-16 Severe Disease \>16
Time frame: week 12
Determine clinical remission rates using SCCAI (Simple Clinical Colitis Activity Index) in patients with Ulcerative Colitis receiving cannabis at week 12
Disease remission will be defined by SCCAI \<3 SCCAI (Simple Clinical Colitis Activity Index) score range from 0 to 19. Higher score means higher disease severity.
Time frame: week 12
Determine clinical remission rates using Harvey-Bradshaw Index (HBI) in Crohn's disease patients receiving cannabis at weeks 24
Disease remission will be defined by HBI \<5 Higher HBI clinical score means higher disease severity: Remission\<5 Mild Disease 5-7 Moderate Disease 8-16 Severe Disease \>16
Time frame: week 24
Determine clinical remission rates SCCAI (Simple Clinical Colitis Activity Index) in patients with Ulcerative Colitis receiving cannabis at week 24
Disease remission will be defined by SCCAI \<3 SCCAI (Simple Clinical Colitis Activity Index) score range from 0 to 19. Higher score means higher disease severity.
Time frame: week 24
Determine endoscopic response rates using Simple Endoscopic Score for Crohn Disease (SES-CD) in patients with Crohn's disease receiving cannabis at weeks 4
Endoscopic response will be defined as decrease of ≥50% in SES-CD score from baseline to week 4 Higher SES-CD score means higher disease activity and severity. A drop \> 50% is considered an endoscopic response
Time frame: week 4
Determine endoscopic response rates using Mayo score in patients with Ulcerative Colitis receiving cannabis at weeks 4
Endoscopic response will be defined as reduction in Endoscopic Mayo score ≤ 1 for Ulcerative Colitis Endoscopic Mayo score range from 0-3. Higher score means higher disease severity
Time frame: week 4
Determine endoscopic response rates using Simple Endoscopic Score for Crohn Disease (SES-CD) in patients with Crohn's disease receiving cannabis at weeks 12
Endoscopic response will be defined as decrease of ≥50% in SES-CD score from baseline to week 12 Higher SES-CD score means higher disease activity and severity. A drop \> 50% is considered an endoscopic response
Time frame: week 12
Determine endoscopic response rates using Mayo score in patients with Ulcerative Colitis receiving cannabis at weeks 12
Endoscopic response will be defined as reduction in Endoscopic Mayo score ≤ 1 for from baseline to week 12 Endoscopic Mayo score range from 0-3. Higher score means higher disease severity
Time frame: week 12
Determine endoscopic response rates using Simple Endoscopic Score for Crohn's Disease (SES-CD) in patients with Crohn's disease receiving cannabis at weeks 24
Endoscopic response will be defined as decrease of ≥50% in SES-CD score from baseline to week 24 Higher SES-CD score means higher disease activity and severity. A drop \> 50% is considered an endoscopic response
Time frame: week 24
Determine endoscopic response rates using Mayo score in patients with Ulcerative Colitis receiving cannabis at weeks 24
Endoscopic response will be defined as reduction in Endoscopic Mayo score ≤ 1 for from baseline to week 24 Endoscopic Mayo score range from 0-3. Higher score means higher disease severity
Time frame: week 24
Determine endoscopic remission rates using Simple Endoscopic Score for Crohn's Disease (SES-CD) in patients with Crohn's disease receiving cannabis at week 4
Endoscopic remission will be defined as SES-CD\<4 for Crohn's disease SES-CD ranges from a minimum score o and has no high limit. Higher SES-CD score means higher disease severity and activity.
Time frame: week 4
Determine endoscopic remission rates using Mayo score in patients with Ulcerative Colitis receiving cannabis at weeks 4
Endoscopic remission will be defined as Endoscopic Mayo score = 0 for ulcerative colitis Endoscopic Mayo score range from 0-3. Higher score means higher disease severity
Time frame: week 4
Determine endoscopic remission rates using Simple Endoscopic Score for Crohn's Disease (SES-CD) in patients with Crohn's disease receiving cannabis at week 12
Endoscopic remission will be defined as SES-CD\<4 for Crohn's disease SES-CD ranges from a minimum score o and has no high limit. Higher SES-CD score means higher disease severity and activity.
Time frame: week 12
Determine endoscopic remission rates using Mayo score in patients with Ulcerative Colitis receiving cannabis at weeks 12
Endoscopic remission will be defined as Endoscopic Mayo score = 0 for ulcerative colitis Endoscopic Mayo score range from 0-3. Higher score means higher disease severity
Time frame: week 12
Determine endoscopic remission rates using Simple Endoscopic Score for Crohn's Disease (SES-CD) in patients with Crohn's disease receiving cannabis at week 24
Endoscopic remission will be defined as SES-CD\<4 for Crohn's disease SES-CD ranges from a minimum score o and has no high limit. Higher SES-CD score means higher disease severity and activity.
Time frame: week 24
Determine endoscopic remission rates using Mayo score in patients with Ulcerative Colitis receiving cannabis at weeks 24
Endoscopic remission will be defined as Endoscopic Mayo score = 0 for Ulcerative Colitis Endoscopic Mayo score range from 0-3. Higher score means higher disease severity
Time frame: week 24
Assess the effect of cannabis treatment on pain levels using visual analog scale (VAS) in patients with IBD, after 1 month of treatment
Pain levels will be measured using pain visual analog scale (VAS) VAS scale range from 0 to 10, where 0 means no pain and higher score means worse pain
Time frame: week 4
Assess the effect of cannabis treatment on pain levels using visual analog scale (VAS) in patients with IBD, after 3 month of treatment
Pain levels will be measured using pain visual analog scale (VAS) VAS scale range from 0 to 10, where 0 means no pain and higher score means worse pain
Time frame: week 12
Assess the effect of cannabis treatment on pain levels using visual analog scale (VAS) in patients with IBD, after 6 month of treatment
Pain levels will be measured using pain visual analog scale (VAS) VAS scale range from 0 to 10, where 0 means no pain and higher score means worse pain
Time frame: week 24
Assess the effect of cannabis treatment on sleep quality using the Pittsburgh Sleep Quality Index (PSQI) in patients with IBD after 1 month of treatment
Sleep quality will be measured using the PSQI PSQI has a range of 0-21; higher score indicate worse sleep quality.
Time frame: week 4
Assess the effect of cannabis treatment on sleep quality using the Pittsburgh Sleep Quality Index (PSQI) in patients with IBD after 3 month of treatment
Sleep quality will be measured using the PSQI PSQI has a range of 0-21; higher score indicate worse sleep quality.
Time frame: week 12
Assess the effect of cannabis treatment on sleep quality using the Pittsburgh Sleep Quality Index (PSQI) in patients with IBD after 6 month of treatment
Sleep quality will be measured using the PSQI PSQI has a range of 0-21; higher score indicate worse sleep quality.
Time frame: week 24
Assess the safety of cannabis treatment in patients with IBD after 1 month of treatment
The safety of cannabis treatment will be measured using Common Terminology Criteria for Adverse Events (CTCAE)
Time frame: 4 weeks
Assess the safety of cannabis treatment in patients with IBD after 3 month of treatment
The safety of cannabis treatment will be measured using Common Terminology Criteria for Adverse Events (CTCAE)
Time frame: 12 weeks
Assess the safety of cannabis treatment in patients with IBD after 6 month of treatment
The safety of cannabis treatment will be measured using Common Terminology Criteria for Adverse Events (CTCAE)
Time frame: 24 weeks
Assess the effect of cannabis treatment on quality of life using medical management questionnaire (IBD self-efficacy scale) in patients with IBD
Quality of life will be measured using IBD self-efficacy scale questionnaire The overall score of the IBD-SES ranges from 29 to 290 with a lower score indicating lower SE.
Time frame: week 24
Assess the effect of cannabis treatment on quality of life Patient Reported Outcomes (PROMIS) questionnaire in patients with IBD
Quality of life will be measured using Patient Reported Outcomes (PROMIS) questionnaire PROMIS measures use T-scores. A higher PROMIS T-score represents more of the concept being measured (negative or positive)
Time frame: week 24
Assess personality traits of patients with IBD favoring cannabis treatment using the Big Five personality traits questionnaire
Personality traits will be measured using the Big Five personality traits questionnaire Each personality type will have a score between 0-40. Higher scores equal stronger personality type.
Time frame: week 24
Started Jul 2019 (actual). Primary completion is estimated for Jul 2023, 48 months after the start.
Of 231 non-industry observational studies under Crohn Disease, half reached primary completion within 47 months of starting (the median), counting those still running; a quarter within 32 and three quarters within 101. This study's planned 48 months is close to that.
Counting every sponsor, half of 304 studies reached it within 42 months; a quarter within 29 and three quarters within 88.
How these figures are worked out, and which studies are left out of them.
This study is status unknown, as verified in Oct 2022. You cannot join it, but the record below documents what was studied.
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Eli Sprecher, MD