Skip to content

Therapeutic Modulation of the Intestinal Creatine Kinase System in Inflammatory Bowel Disease (IBD)

Therapeutic Modulation of the Intestinal Creatine Kinase System in Inflammatory Bowel Disease (IBD)

Status
Withdrawn
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02463305
Enrollment
0
Registered
2015-06-04
Start date
2022-08-31
Completion date
2023-03-01
Last updated
2023-04-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colitis, Ulcerative

Keywords

Colitis, ulcerative, Inflammatory bowel diseases

Brief summary

This study plans to learn more about the effects that creatine monohydrate has on disease activity in ulcerative colitis. Creatine is a substance that is naturally produced by the body and is found in foods, such as meat and fish. Creatine helps to provide energy to some body tissues, such as the colon. In the colon, this energy allows cells to form a tight barrier between molecules in digested food and bacteria and the body's infection-fighting cells within the colon underneath this barrier. If the barrier becomes leaky molecules may pass through and lead to inflammation. This leakiness may contribute to the colon inflammation seen in ulcerative colitis.

Interventions

DRUGCreatine monohydrate

21 grams creatine monohydrate total per day

OTHERPlacebo

7 grams of dextrose dissolved in 500mL water, taken three times daily

Sponsors

University of Colorado, Denver
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Male or female patients aged 18-70 years old with mild- to moderately-active UC that extends at least 15 cm proximal to the anal verge (i.e. not proctitis) as defined by a Mayo Score of 3-10, with an endoscopic subscore ≥ 1. * Allowed concomitant medications will include mesalamine compounds if used for at least 8 weeks and at a stable dose for at least 4 weeks, as well as thiopurines (azathioprine, 6-mercaptopurine) if used at a stable dose for at least 3 months.

Exclusion criteria

* Abnormal baseline laboratory tests: * Albumin \< 3.0 g/dL * ALT, AST, total bilirubin, or alkaline phosphatase \> 1.5 x ULN * Potassium \< 3.0 mmol/L or \> 5.5 mmol/L * Creatinine or cystatin C \> ULN * WBC ≤ 3000 * Platelets ≤ 105 * Hemoglobin ≤ 10g/dL * Positive stool test for Clostridium difficile, ova and parasites, or routine stool culture * Pregnancy (as confirmed by urine pregnancy test at study outset), stated desire to become pregnant during the study period, or refusal/inability to use effective methods of contraception during the study period. * Concomitant major comorbidities (renal, hepatic, cardiac, pulmonary or malignancy) to include any medical conditions requiring therapeutic anti-coagulation or anti-platelet therapy. * Diagnosis of severe UC (Mayo Score \> 10) * Evidence or history of toxic megacolon * Patients who received anti-TNF agents within 3 months of screening, or who used oral or rectal corticosteroids within 4 weeks of screening will be excluded. * Use of over-the-counter herbal or dietary supplements (excluding vitamin and minerals) two weeks prior to or during the study period. * Use of known nephrotoxic medications (including non-steroidal anti-inflammatory drugs (NSAIDs), cyclosporin A, tacrolimus, aminoglycoside antibiotics, diuretics, angiotensin converting enzyme (ACE) inhibitors, or angiotensin receptor blockers) 2 weeks prior to or during the study period * Prior surgical bowel resections (excluding appendectomy) * Local or systemic complications or other pathological states requiring therapy with corticosteroids and/or immunosuppressive agents.

Design outcomes

Primary

MeasureTime frameDescription
Improvement in endoscopic assessment of mucosal inflammation in ulcerative colitis.8 weeksAs defined by the Mayo endoscopic score for ulcerative colitis.

Secondary

MeasureTime frameDescription
Intestinal permeability8 weeksAs measured by urinary saccharide excretion
Patient symptom severity8 weeksAs measured by inflammatory bowel disease questionnaire (IBDQ), simple Crohn's and colitis activity index (SCCAI), and Mayo composite scores.
Colonic inflammation8 weeksAs assessed by fecal calprotectin, CRP, and histologic scoring.
Clinical response in ulcerative colitis disease activity.8 weeksAs defined by the Mayo composite score for ulcerative colitis.
Clinical remission of ulcerative colitis disease activity.8 weeksAs defined by the Mayo composite score for ulcerative colitis.
Creatine modulation8 weeksAs defined by colonic tissue and serum levels.
Creatine kinase modulation8 weeksAs assessed by CK transcript and protein in colonic tissue and serum levels.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026