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The effect of curcumin supplementation in the treatment of patients with ulcerative colitis

The effect of curcumin supplementation on clinical Outcomes, and some Inflammatory Markers in Patients with Ulcerative Colitis

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180207038664N1
Enrollment
70
Registered
2018-04-30
Start date
2018-02-19
Completion date
Unknown
Last updated
2018-05-21

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

Conditions

Ulcerative colitis. Ulcerative colitis

Interventions

Intervention 1: Intervention group:Curcumin supplement, 1500 milligram daily, 3 times per day ,500 milligram capsule each time, for 60 days. Karen Pharma & Food Supplement Co. Intervention 2: Control

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
17 Years to 70 Years

Inclusion criteria

Inclusion criteria: Ulcerative colitis, confirmed by histopathology The severity of the disease is mild to moderate Patients without current diagnosis of other inflammatory, autoimmune and inclusive disease( including cancer, kidney disease, rheumatoid arthritis, liver disease, AIDS, and cardiovascular disease) The age range is between 17-70 years Tendency to participate in the study No changes in the type and amount of drug in the past month The patient should not be pregnant or breastfeeding

Exclusion criteria

Exclusion criteria: The patient is in the acute phase of the disease Reluctance to continue cooperation in this research History of large gastrointestinal surgery (except appendectomy, Cholecystectomy and hemorrhoidectomy) Smoking, alcohol and drug abuse Patients with gallstones or any disorder of the gallbladder, bladder stones

Design outcomes

Primary

MeasureTime frame
Serum hs-CRP. Timepoint: The beginning of the study- The end of the study. Method of measurement: ELISA.;Serum TNF-a. Timepoint: The beginning of the study- The end of the study. Method of measurement: ELISA.;Serum ESR. Timepoint: The beginning of the study- The end of the study. Method of measurement: Westergren's Method.;Stool frequency per day. Timepoint: The beginning of the study- The end of the study. Method of measurement: Mayo Score.;Frequency of rectal bleeding per day. Timepoint: The beginning of the study- The end of the study. Method of measurement: Mayo Score.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNarges Sadeghi

Ahvaz University of Medical Sciences

sadeghi.n@ajums.ac.ir+98 61 3321 4578

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026