Ulcerative Colitis and Vitamin D Supplementation
Primary Purpose
Ulcerative Colitis
Status
Withdrawn
Phase
Phase 1
Locations
Norway
Study Type
Interventional
Intervention
Vitamin D
placebo
Sponsored by
About this trial
This is an interventional treatment trial for Ulcerative Colitis
Eligibility Criteria
Inclusion Criteria:
- Men and women older than18 years old, diagnosed with UC (either debut or relapsed chronic UC), moderate or severe, where it is an indication to treat with infliximab.
Exclusion Criteria:
- Primary hyperparathyroidism (PHPT)
- Sarcoidosis
- Renal failure (serum creatinine > 125 mumol/L in men or > 105 mumol/L in women)
- Those, who use solarium routinely are not included
- Pregnant or breastfeeding women, otherwise women of fertile age must be on approved birth control methods during the study
- Renal stones last 15 years
- Cancer of any origin, diagnosed during last 5 years
- Unstable angina pectoris
Sites / Locations
- University Hospital of North Norway
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Vitamin D
Placebo
Arm Description
Decristol (cholecalciferol) 20000 IU per capsule 1 capsule per week
capsule with peanut oil
Outcomes
Primary Outcome Measures
number of patients with remission
Mandatory criterion of remission: clinical remission (defined as Mayo score <= 1, including endoscopic findings) and non-mandatory: laboratory (calprotectin < 100, WBC and SR within reference range). These criteria will be assessed at 12 month after the start of intervention
Secondary Outcome Measures
change in fecal calprotectin
change in fecal calprotectin compared to baseline value
change in bone mineral density (whole body)
change in bone mineral density in whole body, measured with DEXA (t-score and z-score)
change in fecal calprotectin
change in fecal calprotectin
change in tnf-alpha levels in colonic mucosa
change in mucosal tnf-alpha levels. Biopsies will be taken with the forceps from the colonic mucosa (colon sigmoid) and stored in RNA later media for the further analysis for TNF alpha concentration with PCR method.
change in tnf-alpha (in colonic mucosa)
Biopsies and analysis will be carried out as described ata 3 months follow-up
Full Information
NCT ID
NCT01846026
First Posted
April 30, 2013
Last Updated
June 1, 2015
Sponsor
University Hospital of North Norway
1. Study Identification
Unique Protocol Identification Number
NCT01846026
Brief Title
Ulcerative Colitis and Vitamin D Supplementation
Official Title
Immunomodulating and Clinical Effects of Vitamin D on Remission Induction in Patients With Moderate and Severe Ulcerative Colitis, Undergoing Treatment With Infliximab.
Study Type
Interventional
2. Study Status
Record Verification Date
June 2015
Overall Recruitment Status
Withdrawn
Why Stopped
At the planned study start new treatment guidelines for this disease with new drugs were implemented in clinical practice.
Study Start Date
April 2013 (undefined)
Primary Completion Date
April 2014 (Actual)
Study Completion Date
December 2016 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital of North Norway
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Ulcerative colitis (UC) is an inflammatory disease involving the colonic mucosa, with bleedings and ulcerations. Consequences are destroyed mucosal barrier and increased permeability. Several cytokines are described to mediate the progressive course of ulcerative colitis and it is considered nowadays an immunologic disease. Patients with UC have often low levels of vitamin D and elevated prevalence of osteoporosis.
In vitro studies demonstrate that vitamin D has an immunomodulating effect, and may have a direct healing action on colonic mucosa has been described in animal studies. One can therefore rise a hypothesis that vitamin D supplementation could be crucial in patients with UC. To our knowledge, it has not been performed randomized clinical trials to study these possible effects of vitamin D and it has not been studied the effects of vitamin D on the relapse frequency and immunological composition of colic mucosa in patient with moderate to severe ulcerative colitis.
Objectives for our study are as follows: To examine if high-dose vitamin D supplementation in patients with moderate to severe ulcerative colitis:
reduces relapse frequency and increase the duration of the Infliximab induced remission
mediates and changes the cytokines composition in the colic mucosa
decreases the excretion of calprotectin in feces and reduces the concentration of inflammation markers
augments bone mass
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ulcerative Colitis
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Vitamin D
Arm Type
Experimental
Arm Description
Decristol (cholecalciferol) 20000 IU per capsule
1 capsule per week
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
capsule with peanut oil
Intervention Type
Drug
Intervention Name(s)
Vitamin D
Other Intervention Name(s)
Cholecalciferol
Intervention Description
compare how vitamin D influences the course of ulcerative colitis versus placebo
Intervention Type
Drug
Intervention Name(s)
placebo
Primary Outcome Measure Information:
Title
number of patients with remission
Description
Mandatory criterion of remission: clinical remission (defined as Mayo score <= 1, including endoscopic findings) and non-mandatory: laboratory (calprotectin < 100, WBC and SR within reference range). These criteria will be assessed at 12 month after the start of intervention
Time Frame
12 months after start of intervention
Secondary Outcome Measure Information:
Title
change in fecal calprotectin
Description
change in fecal calprotectin compared to baseline value
Time Frame
12 months after start of intervention
Title
change in bone mineral density (whole body)
Description
change in bone mineral density in whole body, measured with DEXA (t-score and z-score)
Time Frame
12 months after the start of intervention
Title
change in fecal calprotectin
Description
change in fecal calprotectin
Time Frame
3 months
Title
change in tnf-alpha levels in colonic mucosa
Description
change in mucosal tnf-alpha levels. Biopsies will be taken with the forceps from the colonic mucosa (colon sigmoid) and stored in RNA later media for the further analysis for TNF alpha concentration with PCR method.
Time Frame
3 months
Title
change in tnf-alpha (in colonic mucosa)
Description
Biopsies and analysis will be carried out as described ata 3 months follow-up
Time Frame
12 months after baseline
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Men and women older than18 years old, diagnosed with UC (either debut or relapsed chronic UC), moderate or severe, where it is an indication to treat with infliximab.
Exclusion Criteria:
Primary hyperparathyroidism (PHPT)
Sarcoidosis
Renal failure (serum creatinine > 125 mumol/L in men or > 105 mumol/L in women)
Those, who use solarium routinely are not included
Pregnant or breastfeeding women, otherwise women of fertile age must be on approved birth control methods during the study
Renal stones last 15 years
Cancer of any origin, diagnosed during last 5 years
Unstable angina pectoris
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elena Kamycheva, MD, PhD
Organizational Affiliation
Medical Clinic, University Hospital of North Norway
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital of North Norway
City
Tromsø
ZIP/Postal Code
9014
Country
Norway
12. IPD Sharing Statement
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Ulcerative Colitis and Vitamin D Supplementation
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