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The effect of vitamin D supplementation in patients with ulcerative colitis

Study of the effect of vitamin D supplementation on serum vitamin D concentration, quality of life, disease activity index, and some of inflammatory and oxidative factors in patients with ulcerative colitis with vitamin D deficiency

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20100524004010N22
Enrollment
50
Registered
2018-02-01
Start date
2017-04-19
Completion date
Unknown
Last updated
2018-03-26

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

Conditions

ulcerative colitis. Ulcerative colitis, unspecified

Interventions

Intervention 1: vitamin D supplement for 12 weeks 2 pearl contain 1000 IU daily. Intervention 2: One vitamin D supplement 1000 IU daily and one pelacebo for 12 weeks.

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Cases with Ulcerative colitis Active mild to moderate disease severity No evident affliction with other intestinal diseases or disorders, inflammatory diseases and infectious diseases No history of taking supplements such as vitamin D multivitamin-mineral, omega-3, polyphenolic and antioxidants Not taking anti-coagulation drugs such as Heparin and Warfarin or NSAIDs (Non steroidal anti-inflammatory drugs), antihistamines and calcium channel antagonists such as Nifedipine within the past month Patients with vitamin d defficiency (less than 30 nano gram per mili liter) Body mass index (BMI) over than 18.5 and less than 30 kg/m2 Tendency to participate in this research No change in type & dose of drug usage during last month

Exclusion criteria

Exclusion criteria: Pregnancy or lactation in women or use of oral contraceptive drugs The patient Unwillingness to continue participation in this research Drug type and dosage change during intervention

Design outcomes

Primary

MeasureTime frame
Simple Clinical Colitis Activity Index. Timepoint: At the beginning and at the end of the study. Method of measurement: Simple Clinical Colitis Activity Index Questionnaire (SCCAIQ).;Quality of life. Timepoint: At the beginning and at the end of the study. Method of measurement: Inflammatory Bowel Disease Questionnaire -9 (IBDQ-9).;TNF-a. Timepoint: At the beginning and at the end of the study. Method of measurement: ELISA.;Hs-CRP. Timepoint: At the beginning and at the end of the study. Method of measurement: ELISA.;Serum TOC. Timepoint: At the beginning and at the end of the study. Method of measurement: kit.;Serum TAC. Timepoint: At the beginning and at the end of the study. Method of measurement: kit.

Secondary

MeasureTime frame
Vitamin A intake. Timepoint: At the beginning and at the end of the study. Method of measurement: 24h recall questionnaire.;Carbohydrate intake. Timepoint: At the beginning and at the end of the study. Method of measurement: 24h recall questionnaire.;Weight. Timepoint: At the beginning and at the end of the study. Method of measurement: Scale.;Waist circumference. Timepoint: At the beginning and at the end of the study. Method of measurement: Metre.;Hip circumference. Timepoint: At the beginning and at the end of the study. Method of measurement: Metre.;Body Mass Index. Timepoint: At the beginning and at the end of the study. Method of measurement: Calculating.;Total energy intake. Timepoint: At the beginning and at the end of the study. Method of measurement: 24h recall questionnaire.;Protein intake. Timepoint: At the beginning and at the end of the study. Method of measurement: 24h recall questionnaire.;Total fat intake. Timepoint: At the beginning and at the end of the study. Method of measurement: 24h recall questionnaire.;PUFA fatty acid intake (omega 3). Timepoint: At the beginning and at the end of the study. Method of measurement: 24h recall questionnaire.;Cholesterol intake. Timepoint: At the beginning and at the end of the study. Method of measurement: 24h recall questionnaire.;Fiber intake. Timepoint: At the beginning and at the end of the study. Method of measurement: 24h recall questionnaire.;SFA fatty acid intake. Timepoint: At the beginning and at the end of the study. Method of measurement: 24h recall questionnaire.;MUFA fatty acid intake. Timepoint: At the beginning and at the end of the study. Method of measurement: 24h recall questionnaire.;PUFA fatty acid intake (omega 6). Timepoint: At the beginning and at the end of the study. Method of measurement: 24h recall questionnaire.;Vitamin E intake. Timepoint: At the beginning and at the end of the study. Method of measurement: 24h recall questionnaire.;VitaminC intake. Timepoint: At the beginning and

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAzita Hekmatdoost

Shahid Beheshti Nutrition Faculty

A_hekmat2000@yahoo.com+98 21 2237 6480

Outcome results

None listed

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