A Phase 2 interventional study of Methylnaltrexone and Placebo in Postoperative Ileus, sponsored by Ohio State University. Completed at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2021-10-27.
Sponsored by Ohio State University · Phase 2, Interventional, and Prevention
This randomized controlled trial will prospectively evaluate the clinical benefit for subcutaneous methylnaltrexone (MNTX) in counteracting the obstipatory (causing constipation) effects of spinal surgery without increasing narcotic usage or otherwise disrupting the recovery course of patients. Using a double-blind randomized design, either subcutaneous MNTX (0.15 mg/kg rounded to 8 mg or 12 mg) or placebo will be administered starting before surgery and then daily for three days. Information will be collected from medical records in IHIS up to 30 days prior to surgery and then for up to 30 days after surgery.
Postoperative Ileus refers to the transient interruption of propulsive motor activity of the gastrointestinal (GI) tract that prevents effective movement of its contents and tolerance of oral intake. Although POI is generally considered to significantly increase hospital stays and inpatient costs after spinal surgery, the incidence, associated risk factors, and effective preventative strategies remain poorly characterized. The proposed etiologies underlying POI are broad and remain incompletely characterized. They include post surgical sympathetic nervous system activation, inflammatory factors, and the effects of analgesics on GI tract motility. Treatment often consists of aggressive bowel regimens, nasogastric tube insertion for decompression, and the application of various laxatives, suppositories, and enemas. The widespread use of these measures is unfortunately not supported by high level evidence. The incidence of POI after spinal fusion is reported to range between 0.6 to 16.7%. This estimated range likely represents a gross underestimate of POI given the retrospective nature of studies undertaken to date. Fineberg and colleagues reported that the risk increases nearly 3-fold following anterior lumbar spinal fusions as compared to posterior surgeries. Furthermore, the only risk factors they identified to be correlated with POI is male gender, = 3 fusion levels, alcohol abuse, anemia, electrolyte abnormalities, and weight loss. Kiely and colleagues found that ileus was associated with the administration of certain intravenous solutions such as lactated ringers and sodium chloride. Interestingly, they found that albumin administration was associated with a reduced incidence of ileus postoperatively. Lee and colleagues evaluated POI following orthopedic surgery and reported an incidence of 2.1%. They found that patients who developed POI were more likely to be older, had higher blood loss during surgery, and also had higher rates of preoperative constipation. This study, however, included all types of orthopedic surgeries (not limited to spinal fusion). Early clinical studies evaluated the effectiveness of MNTX in treating opioid-induced constipation (OIC). Several clinical trials confirmed that MNTX was well tolerated and counteracted the GI effects of opioids, thereby enhancing gut motility without inhibiting their analgesic properties. Only two studies to date have evaluated the potential effectiveness of MNTX in reducing the incidence of POI following GI surgery. Both studies were unfortunately hampered by serious design flaws. Most importantly, neither study included pre-operative administration of MNTX. As such, MNTX remains at this time approved only for chronic OIC based on two double-blind, randomized, placebo-controlled trials conducted in patients with advanced illness wherein MNTX rapidly induced laxation as compared to placebo.
167 studies on the registry are indexed under Ileus; 23 are open to participants now.
This study's enrollment of 82 is close to the median of 90 across 138 interventional studies indexed under Ileus.
Browse Ileus studies →Ohio State University is the lead sponsor of 663 studies on the registry; 148 are open to participants now.
Of its 67 completed or terminated interventional studies of FDA-regulated products, 49 (73%) have results posted.
Counted across the registry records on this site, refreshed daily.
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.
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.
Relapsed: the illness came back after treatment had worked. Refractory: it did not respond to treatment, or stopped responding while still on it.
Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.
GFR (glomerular filtration rate) is how much blood the kidneys filter each minute. It is usually estimated from a blood test — eGFR, by formulas such as CKD-EPI or MDRD — and some studies ask for it to be measured directly instead. Usually given in mL/min/1.73 m².
Check the method, the units and the minimum the study states. A value of 90 or above is in the normal-or-high range, but kidney damage can show in other tests too.
A drug or device being studied in a clinical trial.
It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.
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.
Relapsed and refractory
Relapsed: the illness came back after treatment had worked. Refractory: it did not respond to treatment, or stopped responding while still on it.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Clinically significant
Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
GFR and eGFR (kidney filtering)
GFR (glomerular filtration rate) is how much blood the kidneys filter each minute. It is usually estimated from a blood test — eGFR, by formulas such as CKD-EPI or MDRD — and some studies ask for it to be measured directly instead. Usually given in mL/min/1.73 m².
Check the method, the units and the minimum the study states. A value of 90 or above is in the normal-or-high range, but kidney damage can show in other tests too.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Investigational drug or device
A drug or device being studied in a clinical trial.
It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
The study arm will receive subcutaneous methylnaltrexone (0.15mg/kg rounded to 8 or 12 mg) before surgery and then daily, for the following three days after surgery (four doses).
Drug: Methylnaltrexone
The placebo arm will receive subcutaneous placebo before surgery and then daily, for the following three days after surgery (four doses).
Other: Placebo
Randomization of methylnaltrexone to placebo will be at a 1:1 ratio. Those receiving methylnaltrexone (study drug) will receive a subcutaneous dose pre-surgery and daily for three days following surgery.
Randomization of methylnaltrexone to placebo will be at a 1:1 ratio. Those receiving placebo will receive a subcutaneous dose pre-surgery and daily for three days following surgery.
Time to First Bowel Movement
The time it takes for the participant to have a bowel movement from the end of surgery.
Time frame: 30 days post-operative
Time to Discharge
The number of hours it takes for the participant to meet all discharge criteria and be released from the hospital.(Time-to-discharge/discharge eligibility)
Time frame: 30 Days post-operative
Time to Discharge
The time it takes for the participant to discharge
Time frame: 30 Days post-operative
Daily Narcotics
The amount of daily narcotics (in morphine milli-equivalents) given to a patient (average of post op day 1 - 3)
Time frame: 30 days post-operative
| Milestone | Study Arm: Methylnaltrexone | Placebo Arm |
|---|---|---|
| Started | 41 | 41 |
| Completed | 41 | 41 |
| Not completed | 0 | 0 |
The time it takes for the participant to have a bowel movement from the end of surgery.
| hours | Study Arm: Methylnaltrexone | Placebo Arm |
|---|---|---|
| Time to First Bowel Movement | 61.8 (35.7 to 93.6) | 50.7 (17.8 to 110.8) |
The number of hours it takes for the participant to meet all discharge criteria and be released from the hospital.(Time-to-discharge/discharge eligibility)
| Hours | Study Arm: Methylnaltrexone | Placebo Arm |
|---|---|---|
| Time to Discharge | 105.0 (84.6 to 110.2) | 90.7 (85.4 to 111.3) |
The time it takes for the participant to discharge
| Days | Study Arm: Methylnaltrexone | Placebo Arm |
|---|---|---|
| Time to Discharge | 4.29 (3.38 to 8.39) | 4.19 (3.23 to 7.69) |
The amount of daily narcotics (in morphine milli-equivalents) given to a patient (average of post op day 1 - 3)
| MME | Study Arm: Methylnaltrexone | Placebo Arm |
|---|---|---|
| Daily Narcotics | 136.8 (107.9 to 168.6) | 148.5 (94.8 to 203.7) |
Collected over Immediately pre-operative to 30 Days post-operative. Non-serious events are listed at a 0% frequency threshold.
| Group | Deaths | Serious | Other |
|---|---|---|---|
| Study Arm: Methylnaltrexone | 0/41 (0%) | 6/41 (14.6%) | 11/41 (26.8%) |
| Placebo Arm | 0/41 (0%) | 7/41 (17.1%) | 7/41 (17.1%) |
| Event | Study Arm: Methylnaltrexone | Placebo Arm |
|---|---|---|
| Migratory artheralgias/ gout flare upImmune system disorders | 0/41 | 2/41 |
| Disorientation/ Hallucinations secondary to alcohol withdrawalPsychiatric disorders | 0/41 | 1/41 |
| Abdominal PainGastrointestinal disorders | 0/41 | 1/41 |
| Wound DehiscenceInfections and infestations | 0/41 | 1/41 |
| StrokeVascular disorders | 0/41 | 1/41 |
| Non-ST-elevation myocardial infarction (NSTEMI)Cardiac disorders | 0/41 | 1/41 |
| Altered mental status (AMS)Psychiatric disorders | 1/41 | 1/41 |
| hypoxemia, loss of responseBlood and lymphatic system disorders | 1/41 | 0/41 |
| Syncope; dehydration; Fracture- Right footSocial circumstances | 1/41 | 0/41 |
| Post-Operative IleusGastrointestinal disorders | 1/41 | 0/41 |
| Event | Study Arm: Methylnaltrexone | Placebo Arm |
|---|---|---|
| > 3 bowel movements in 1 dayGastrointestinal disorders | 4/41 | 1/41 |
| Wound dehiscence / drainage from incisionInfections and infestations | 2/41 | 2/41 |
| AMS and emesis during attempted bowel movement.Psychiatric disorders | 1/41 | 0/41 |
| Hemoglobin dropBlood and lymphatic system disorders | 1/41 | 0/41 |
| Intraoperatively, a Cerebrospinal Fluid (CSF) leak was noted.Surgical and medical procedures | 1/41 | 0/41 |
| Diagnosis of Acute Kidney InjuryRenal and urinary disorders | 1/41 | 0/41 |
| Post-operative illeusGastrointestinal disorders | 1/41 | 1/41 |
| increasing pain with concern for infection without drainage or disMusculoskeletal and connective tissue disorders | 1/41 | 0/41 |
| Hypotension, syncopeCardiac disorders | 0/41 | 1/41 |
| Kidney Disease Improving Global Outcomes Stage III (kidney disease)Renal and urinary disorders | 0/41 | 1/41 |
| Age, Categorical(Participants) | Study Arm: Methylnaltrexone | Placebo Arm | Total |
|---|---|---|---|
| <=18 years | 0 | 0 | 0 |
| Between 18 and 65 years | 29 | 28 | 57 |
| >=65 years | 12 | 13 | 25 |
| Age, Continuous(years) | Study Arm: Methylnaltrexone | Placebo Arm | Total |
|---|---|---|---|
| Mean | 61.8 ± 10.2 | 60.8 ± 10.0 | 61.3 ± 10.0 |
| Sex: Female, Male(Participants) | Study Arm: Methylnaltrexone | Placebo Arm | Total |
|---|---|---|---|
| Female | 21 | 23 | 44 |
| Male | 20 | 18 | 38 |
| Ethnicity (NIH/OMB)(Participants) | Study Arm: Methylnaltrexone | Placebo Arm | Total |
|---|---|---|---|
| Hispanic or Latino | 0 | 1 | 1 |
| Not Hispanic or Latino | 40 | 38 | 78 |
| Unknown or Not Reported | 1 | 2 | 3 |
| Race (NIH/OMB)(Participants) | Study Arm: Methylnaltrexone | Placebo Arm | Total |
|---|---|---|---|
| American Indian or Alaska Native | 0 | 0 | 0 |
| Asian | 1 | 0 | 1 |
| Native Hawaiian or Other Pacific Islander | 0 | 0 | 0 |
| Black or African American | 2 | 7 | 9 |
| White | 38 | 34 | 72 |
| More than one race | 0 | 0 | 0 |
| Unknown or Not Reported | 0 | 0 | 0 |
| Region of Enrollment(participants) | Study Arm: Methylnaltrexone | Placebo Arm | Total |
|---|---|---|---|
| United States | 41 | 41 | 82 |
PDFs hosted by the registry, ClinicalTrials.gov.
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Studies of the drug tested here: Methylnaltrexone