Bio-enhanced Curcumin as an Add-on Treatment in Maintaining Remission of Ulcerative Colitis

Phase 3

• Conditions: Ulcerative Colitis
• Interventions: Dietary Supplement: Bio-enhanced Curcumin Soft Gelatin Capsule; Drug: 5-Aminosalicyclic acid

• Registration Number: NCT02683759
• Lead Sponsor: Asian Institute of Gastroenterology, India

Brief Summary

Inflammatory Bowel Disease, including ulcerative colitis, is thought to result from an imbalance of pro-inflammatory and anti-inflammatory factors. As such, the majority of treatment options are directed at attempting to control the chronic inflammation and prolonging remission of clinical symptoms. Several studies have proven that curcumin has well-established anti-inflammatory properties. However, curcumin has poor bioavailability and prior studies have needed to use high concentrations in order to study the efficacy of the product. The investigators propose that a bio-enhanced preparation of curcumin will require a lower dosage to reach and affect its target tissue and will subsequently produce less adverse side effects.

Detailed Description

Not available

Study Timeline

• Status Verified: 2016-02
• Study Start: 2016-02
• Study First Submitted: 2016-02-10
• Study First Submitted QC: 2016-02-12
• Study First Posted: 2016-02-17
• Last Update Submitted: 2016-02-20
• Last Update Posted: 2016-02-23
• Primary Completion: 2017-02

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

• Patients who have been in symptomatic remission from Ulcerative Colitis for at least 3 months. This is defined as a Partial Mayo Index Score of 0 or 1
• Age 18 years and above
• Male or female
• Patients who are able and willing to follow the treatment given and record responses in survey form

Exclusion Criteria

• Patients who are currently experiencing symptomatic flares of mild or moderate ulcerative colitis, or have a partial mayo index score of 2 or greater
• Patients who have been taking azathioprine or mercaptopurine for <12 weeks for the treatment of their ulcerative colitis
• Patients who are taking steroids, immunosuppressants, or biologic agents for the treatment of their ulcerative colitis
• Patients who have severe ulcerative colitis
• Patients who are noncompliant with medication or regular follow up visits
• Patients who are unable or unwilling to record their responses in survey form
• Patients with comorbid illnesses, including: Diabetes Mellitus, Stage III or above Congestive Heart Failure, chronic pancreatitis, severe liver or renal disease
• Patients who have current gallstones or biliary dysfunction
• Patients with anemia (Hemoglobin <10), thrombocytopenia, abnormal lymphocyte counts, or coagulation abnormalities
• Patients with current sepsis or current ongoing infection, including C. difficile colitis or enteritis
• Patients with a history of malignancy
• Patients who are currently pregnant or nursing
• Patients who are current smokers

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Treatment Arm	Bio-enhanced Curcumin Soft Gelatin Capsule	Patients will receive 5-Aminosalicyclic acid as per their current treatment regimen and will also take Bio-enhanced curcumin twice daily after meals as per the following regimen:
Control Arm	5-Aminosalicyclic acid	Patients will receive 5-Aminosalicyclic acid as per their current treatment regimen and will also take a placebo pill twice daily after meals
Treatment Arm	5-Aminosalicyclic acid	Patients will receive 5-Aminosalicyclic acid as per their current treatment regimen and will also take Bio-enhanced curcumin twice daily after meals as per the following regimen:

Primary Outcome Measures

Name	Time	Method
Percentage of patients who remained in clinical remission in the treatment arm compared with percentage of patients who remained in clinical remission in the control arm	1 year	Clinical remission is recorded by a Partial Mayo Index score of 0-1
Percentage of patients who remained in endoscopic remission in the treatment arm compared with percentage of patients who remained in endoscopic remission in the control arm	1 year	Endoscopic remission is defined as endoscopic mucosal healing, is recorded by a Ulcerative Colitis Endoscopic Index of Severity (UCEIS) score of \<3

Secondary Outcome Measures

Name	Time	Method
Percentage of patients in the treatment arm who experienced adverse events as compared with patients in the placebo arm	1 year

Trial Locations

Locations (1)

Asian Institutes of Gastroenterology; 🇮🇳 Hyderabad, Telangana, India