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TerminatedNCT00805285Updated Dec 4, 2019Results posted

The Use of Oral Budesonide and Rectal Hydrocortisone for the Treatment of Active Ulcerative Colitis

A Phase 2 interventional study of Combination Oral Budesonide and Rectal Hydrocortisone in Inflammatory Bowel Disease and Ulcerative Colitis, sponsored by University of Maryland, Baltimore. Terminated at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2019-12-04.

Sponsored by University of Maryland, Baltimore · Phase 2, Interventional, and Treatment

Why this study was terminated
Study terminated due to insufficient enrollment
Phase
Phase 2
Study type
Interventional
Enrollment
1
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of this study is to evaluate if the combination of oral budesonide and rectal hydrocortisone improves symptoms in patients with active ulcerative colitis. Also, we would like to determine if oral budesonide and rectal hydrocortisone has fewer and less severe side effects compared to standard steroids (prednisone).

Read the detailed description

Ulcerative colitis (UC) is a common chronic inflammatory condition of the intestines that results in bloody diarrhea, abdominal pain, and extraintestinal manifestations of disease. The disease course is typically chronic, characterized by periodic exacerbations followed by symptom- free intervals; less commonly symptoms are continuous and unrelenting. The symptoms and disease course have a profound, detrimental impact on the quality of life in patients with UC.

The initial therapeutic approach depends upon both the extent of colonic involvement and the severity of the disease process at presentation. Typically, patients are treated based on a pyramid or "Step up" approach. If patients have mild symptoms, they receive less powerful therapies lower in the pyramid with fewer side effects. Patients with disease confined to distal colon are typically treated with topical therapies including either 5-ASA or steroid enemas. However, as symptoms worsen or if severe at the time of diagnosis, patients receive more aggressive therapies higher in the pyramid including steroids. Despite medical therapy, 50% will have colectomy or become steroid dependent one year after receiving steroids.

Steroids are associated with significant side effects. Adverse consequences of steroids are related to dose and duration of exposure, and include but are not limited to cosmetic side effects, ocular disease (glaucoma, cataracts), diabetes, hypertension, vascular disease, osteoporosis, neuropsychiatric complications, and increased risk of infection.

Newer "designer" corticosteroids including budesonide have reduced systemic bioavailability and high local anti-inflammatory activity; as a result it is associated with fewer and less severe side effects. Studies have proven the efficacy of budesonide in inducing remission in active Crohn's disease. However, the data for the use of oral budesonide in patients with UC is less extensive. However, the data regarding the efficacy of topical therapy for left-sided UC is extensive. Randomized controlled trials of budesonide enemas have demonstrated similar efficacy and safety profile to hydrocortisone enemas in the induction of remission of left sided UC. We have chosen to utilize hydrocortisone enemas in our study as it is widely available in the United States.

A 52-week open-label pilot study will be performed at the University of Maryland Medical Center. Subjects will include patients with previously or newly diagnosed extensive ulcerative colitis. Patients will be treated with oral budesonide and rectal hydrocortisone for 8 weeks followed by a predetermined taper. All patients will undergo research clinic visits at enrollment and week 8. During these visits, patients will complete a series of questionnaires that measure the patient's disease activity, quality of life, side effects, medical compliance, and other parameters. Blood draws and stool studies are required at each study visit to monitor blood counts, electrolytes, liver function, inflammatory markers, and adrenal function. Additionally, at week 16, an ACTH (cosyntropin) stimulation test will be performed. After obtaining a basal cortisol level, 250 ug of cosyntropin is given intravenously. Plasma samples of cortisol will then be drawn at 30 minutes to assess for adrenal insufficiency. Close follow-up with eight 30-min telephone sessions (every 2-3 weeks) will also be conducted to assess disease activity and adverse events.

The goal of this study is to determine whether combination therapy using oral budesonide and topical hydrocortisone will result in the induction of remission in patients with active extensive ulcerative colitis. Further, we aim to show that combination therapy is better tolerated and has less severe side effects compared to conventional therapy with prednisone.

02

Conditions studied

  • Inflammatory Bowel Disease
  • Ulcerative Colitis

Keywords

  • Inflammatory Bowel Disease
  • Ulcerative Colitis
  • Budesonide
  • Corticosteroids
03

In context

Colitis

1,073 studies on the registry are indexed under Colitis; 131 are open to participants now.

This study's enrollment of 1 is below the median of 60 across 771 interventional studies indexed under Colitis.

Browse Colitis studies →

Lead sponsor

University of Maryland, Baltimore is the lead sponsor of 687 studies on the registry; 130 are open to participants now.

Of its 90 completed or terminated interventional studies of FDA-regulated products, 63 (70%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Written, voluntary, informed consent given
  • 18 years or older
  • Speak and read English
  • Extensive ulcerative colitis based upon endoscopy, histopathology, and clinical symptoms
  • SCCAI Score > 3
  • Presence of diarrhea (3 or more bowel movements per 24 hours) AND grossly visible blood in stool

Exclusion criteria

Exclusion Criteria:

  • Serum creatinine > 2.0 mg/dL
  • Pregnant or breastfeeding
  • Prior history of total or subtotal colectomy, or currently has an ostomy
  • History or suspicion of Crohn's disease or Indeterminate colitis
  • Diagnosis of any condition deemed by the investigator inhibiting completion of the trial
  • Initiated therapy with or change in mesalamine dose within the last 4 weeks
  • Change in azathioprine, 6-mercaptopurine, or cyclosporine within the last 8 weeks
  • Currently taking or have used corticosteroids within the last 8 weeks
  • Rectally administered mesalamine or steroids within the last 2 weeks
  • Current or prior use of anti-TNF alpha agents within the last 8 weeks
  • Experimental ulcerative colitis agents within the last 8 weeks
  • Concomitant use of CYP3A4 activity inhibitor (e.g. ketoconazole, itraconazole, ritonavir, indinavir, erythromycin)
  • Uncontrolled diabetes (HgA1c > 8.0) within 1 year
  • Unstable Coronary artery disease/Class III/IV CHF
  • Decompensated cirrhosis (e.g. encephalopathy, renal failure, ascites, GIB)
  • Any known infection requiring antibiotics
  • Active Clostridium difficile infection
  • COPD requiring home oxygen
  • HIV/AIDS with CD4 \< 200 or AIDs-defining illnesses/infections
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
1 participant (actual)

Study arms

  • Experimental
    Combination Oral Budesonide and Rectal Hydrocortisone

    See intervention

    Drug: Combination Oral Budesonide and Rectal Hydrocortisone

Interventions

  • DrugCombination Oral Budesonide and Rectal Hydrocortisone

    Budesonide 9 mg PO (oral) daily and hydrocortisone 100 mL PR (enema) for an 8-week period. The doses of each drug to be used in the pilot study are standard doses used in clinical practice. After 8-weeks, the budesonide will be tapered in the following manner: 1) budesonide 6 mg PO daily and hydrocortisone 100 ml PR every other day (EOD) for 3 weeks then 2) budesonide 3 mg PO daily and hydrocortisone 100 ml PR 2 x per week for 3 weeks then 3) discontinue budesonide.

    Also known as: Entocort

06

What researchers measure

Primary outcomes

  1. Simple Clinical Colitis Disease Activity (SCCAI)

    Scores range from 0-19. Higher scores indicated increased disease severity. A score less than 3 is consistent with clinical remission.

    Time frame: 0, 2, 4, 6, and 8 weeks

  2. Short Inflammatory Bowel Disease Questionnaire (SIBDQ)

    Scores range from 10-70 where higher scores indicated better quality of life.

    Time frame: Week 0 and 8

Secondary outcomes

  1. ACTH Stimulation Test

    An increase in cortisol after stimulation by ACTH is normal. Blood cortisol after ACTH stimulation should be greater than 18 - 20 mcg/dL, depending on the dose of cosyntropin used.

    Time frame: Week 16

  2. Adverse Events

    Time frame: 0, 2, 4, 6, 8, 11, 14, 20, 26, and 52 weeks

  3. C Reactive Protein

    Higher values indicated increased disease activity

    Time frame: Week 0 and 8

07

Results

Posted May 13, 2013
Limitations and caveats
The study was terminated early by the University of Maryland HRPO secondary to limited recruitment of participants. This resulted in an inability to analyze the results.

Participant flow

Participant flow — Overall Study
MilestoneCombination Oral Budesonide and Rectal Hydrocortisone
Started1
Completed0
Not completed1
Withdrew: Lack of efficacy1

Outcome measures

PrimarySimple Clinical Colitis Disease Activity (SCCAI)

Scores range from 0-19. Higher scores indicated increased disease severity. A score less than 3 is consistent with clinical remission.

Time frame:
0, 2, 4, 6, and 8 weeks

No measurements were reported for this outcome.

PrimaryShort Inflammatory Bowel Disease Questionnaire (SIBDQ)

Scores range from 10-70 where higher scores indicated better quality of life.

Time frame:
Week 0 and 8

No measurements were reported for this outcome.

SecondaryACTH Stimulation Test

An increase in cortisol after stimulation by ACTH is normal. Blood cortisol after ACTH stimulation should be greater than 18 - 20 mcg/dL, depending on the dose of cosyntropin used.

Time frame:
Week 16

No measurements were reported for this outcome.

SecondaryAdverse Events
Time frame:
0, 2, 4, 6, 8, 11, 14, 20, 26, and 52 weeks
Reported as:
Number · Adverse events
Adverse Events
Adverse eventsCombination Oral Budesonide and Rectal Hydrocortisone
Adverse Events2
SecondaryC Reactive Protein

Higher values indicated increased disease activity

Time frame:
Week 0 and 8

No measurements were reported for this outcome.

Adverse events

Non-serious events are listed at a 5% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Combination Oral Budesonide and Rectal Hydrocortisone—1/1 (100%)1/1 (100%)
Most frequent serious events
Most frequent serious events
EventCombination Oral Budesonide and Rectal Hydrocortisone
Worsening of ulcerative colitisGastrointestinal disorders1/1
Most frequent other events
Most frequent other events
EventCombination Oral Budesonide and Rectal Hydrocortisone
Portal vein and superior mesenteric vein thrombosisVascular disorders1/1

Baseline characteristics

The only enrolled patient was withdrawn secondary to disease worsening.

Age, Categorical
Age, Categorical(Participants)Combination Oral Budesonide and Rectal Hydrocortisone
<=18 years0
Between 18 and 65 years1
>=65 years0
Age, Continuous
Age, Continuous(years)Combination Oral Budesonide and Rectal Hydrocortisone
Mean45 ± 0
Sex: Female, Male
Sex: Female, Male(Participants)Combination Oral Budesonide and Rectal Hydrocortisone
Female1
Male0
Region of Enrollment
Region of Enrollment(participants)Combination Oral Budesonide and Rectal Hydrocortisone
United States1
08

Study locations

1 site
  • University of Maryland
    Baltimore, Maryland 21201, United States
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 4, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00805285
Lead sponsor
University of Maryland, Baltimore
Responsible party
Raymond Cross (Principal Investigator, University of Maryland, Baltimore) — Principal investigator
First posted
Dec 9, 2008
Start date
Oct 2008
Primary completion
Oct 2009
Completion
Mar 2010
Results posted
May 13, 2013
Last update
Dec 4, 2019

Study contacts

Raymond K Cross, MD, MS
principal investigator · University of Maryland, College Park
Leyla J Ghazi, MD
study chair · University of Maryland, College Park

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

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This study is terminated, as verified in Nov 2019. You cannot join it, but the record below documents what was studied.

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