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Cholecalciferol in Chronic Inflammatory Bowel Diseases (5C)

Primary Purpose

IBD

Status
Recruiting
Phase
Phase 3
Locations
Switzerland
Study Type
Interventional
Intervention
D3 VitaCaps®
Sponsored by
University Hospital, Basel, Switzerland
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for IBD

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Confirmed IBD diagnosis; Age ≥ 18 years Exclusion Criteria: Hypercalcaemia defined as serum calcium value >2.70 mmol/l; Hyperparathyreoidism defined as serum iPTH value >65 ng/l; Hypoparathyreoidism defined as serum iPTH value <15 ng/l; Renal insufficiency defined as eGFR < 30 ml/min; Anamnesis of: Propensity to form calcium-containing kidney stones, Impaired renal calcium or phosphate excretion, Sarcoidosis; Pregnancy or lactation; Supplementation of vitamin D >200 IU/d (5μg/d) during study period; Administration of products that have a potential interaction with cholecalciferol, e.g. phenytoin, rifampicin, barbiturates, actinomycin, imidazole-antifungals

Sites / Locations

  • Clarunis University Center for Gastrointestinal and Liver DiseasesRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

No Intervention

Arm Label

Weekly

Monthly

Control

Arm Description

weekly administration of one capsule, corresponding to approximately 3'500 IU cholecalciferol daily.

monthly administration of one capsule, corresponding to approximately 800 IU cholecalciferol daily.

no treatment

Outcomes

Primary Outcome Measures

Faecal calprotectin value
Reduction of the faecal calprotectin value after 6 months.

Secondary Outcome Measures

CRP serum levels
Change in CRP serum levels after 6 months.
Vitamin D levels
Increase in vitamin D levels after 6 months.
Disease-specific activity score
Change in disease-specific activity score after 6 months.
Adherence to the comedication
Adherence to the comedication with the vitamin D capsules

Full Information

First Posted
November 14, 2022
Last Updated
November 28, 2022
Sponsor
University Hospital, Basel, Switzerland
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1. Study Identification

Unique Protocol Identification Number
NCT05624801
Brief Title
Cholecalciferol in Chronic Inflammatory Bowel Diseases
Acronym
5C
Official Title
Cholecalciferol Comedication in Patients With Chronic Inflammatory Bowel Diseases (Crohn's Disease or Ulcerative Colitis) - the 5C-study
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 1, 2022 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Basel, Switzerland

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
In this research project, the investigators want to find out whether the additional intake of vitamin D further reduces the inflammatory events in the intestines of IBD patients. There are three groups of subjects: the 1st group takes a capsule of 24,000 IU per week, the 2nd group takes 24,000 IU per month, the 3rd group is the control group. The intake extends over 6 months during the autumn and winter period.
Detailed Description
Inflammatory bowel diseases (IBD) are a chronic immunologically mediated inflammatory condition of the gastrointestinal tract comprising two clinical entities: ulcerative colitis and Crohn's disease. Genetic,environmental and microbial factors, and the immune responses play an important role in the disease development. The incidence and prevalence of IBD have increased in the past 50 years in the Western world and are increasing in developing countries. Faecal calprotectin is a reliable biomarker for functional quantitative measurement of intestinal inflammation in IBD. Faecal calprotectin test is recognized to be reliable in clinical practice for the assessment of endoscopic activity and remission. Vitamin D or cholecalciferol is a prohormone classified as a fat-soluble vitamin. The organism can produce the substance itself in the skin during summer time. The importance of vitamin D for the regulation of calcium metabolism, for bone formation, for the treatment of osteoporosis and for the prevention of falls and associated fractures is generally recognized. Vitamin D seems to play a role in the pathogenesis of many diseases,including IBD. Several observational studies showed an inverse correlation between 25(OH)D and disease activity. Vitamin D deficiency is common among patients with IBD. The relapse rate in patients with Crohn' disease and 25(OH)D <50 nmol/l is almost doubled. There is a significant inverse correlation between serum 25(OH)D levels and the specific inflammatory marker faecal calprotectin. The lowest serum 25(OH)D levels have been reported in patients with a more severe disease progression or previous ileum resection. Low 25(OH)D serum concentrations are associated with more frequent IBDassociated surgeries and hospitalisations. However, no intervention studies have been conducted to date that have investigated the influence of vitamin D on inflammation in adult IBD patients. An intervention study with subjects aged 5-18 years nevertheless showed a statistically significant inverse correlation between 25(OH)D serum concentration and the inflammation marker calprotectin. The FOPH Expert Commission recommends a daily intake of 600 IU for adults aged 19-59 years, 800 IU for >60 years. The maximum tolerable intake for all age groups is 4'000 IU daily, with daily or cumulative intermittent, weekly or monthly, administration being considered. Adherence is, however, better with intermittent intake. In this study, the administration to patients with monthly supplementation represents one capsule per month, corresponding to 800 IU cholecalciferol daily. The administration to patients with weekly supplementation is one capsule per week, corresponding to 3,500 IU cholecalciferol daily. The cumulative administration of 24'000 IU per week does not exceed the upper limit of 4'000 IU per day or 28'000 IU per week. Insufficient adherence to IBD medication has been identified as responsible for therapy escalation with more expensive regimens, disease complication or hospitalization, that all drive substantial costs. In a systematic review including 93'998 patients with IBD, adherence rate to prescribed biologics ranged from 37% to 96%. Difficulties with medication adherence can be identified with indirect methods such as questionnaires. To monitor adherence, questionnaires and pill-count are the most frequently used methods. However, more robust methods are recommended such as electronic methods. One option is the use of a e-pill bottles with electronic caps. The opening of the e-pill-bottle that corresponds to the withdrawal of a medicine from the container is registered with a time stamp, a method currently in development in our research group.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
IBD

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Weekly
Arm Type
Active Comparator
Arm Description
weekly administration of one capsule, corresponding to approximately 3'500 IU cholecalciferol daily.
Arm Title
Monthly
Arm Type
Active Comparator
Arm Description
monthly administration of one capsule, corresponding to approximately 800 IU cholecalciferol daily.
Arm Title
Control
Arm Type
No Intervention
Arm Description
no treatment
Intervention Type
Drug
Intervention Name(s)
D3 VitaCaps®
Other Intervention Name(s)
Vitamin D
Intervention Description
Gelatine free soft capsules containing 24'000 IU cholecalciferol per capsule
Primary Outcome Measure Information:
Title
Faecal calprotectin value
Description
Reduction of the faecal calprotectin value after 6 months.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
CRP serum levels
Description
Change in CRP serum levels after 6 months.
Time Frame
6 months
Title
Vitamin D levels
Description
Increase in vitamin D levels after 6 months.
Time Frame
6 months
Title
Disease-specific activity score
Description
Change in disease-specific activity score after 6 months.
Time Frame
6 months
Title
Adherence to the comedication
Description
Adherence to the comedication with the vitamin D capsules
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Confirmed IBD diagnosis; Age ≥ 18 years Exclusion Criteria: Hypercalcaemia defined as serum calcium value >2.70 mmol/l; Hyperparathyreoidism defined as serum iPTH value >65 ng/l; Hypoparathyreoidism defined as serum iPTH value <15 ng/l; Renal insufficiency defined as eGFR < 30 ml/min; Anamnesis of: Propensity to form calcium-containing kidney stones, Impaired renal calcium or phosphate excretion, Sarcoidosis; Pregnancy or lactation; Supplementation of vitamin D >200 IU/d (5μg/d) during study period; Administration of products that have a potential interaction with cholecalciferol, e.g. phenytoin, rifampicin, barbiturates, actinomycin, imidazole-antifungals
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Petr Hrúz, Prof. Dr.
Phone
+41 61 777 74 19
Email
petr.hruz@clarunis.ch
First Name & Middle Initial & Last Name or Official Title & Degree
Jean-Pierre Rothen, Dr.
Phone
+41 61 207 61 75
Email
jp.rothen@unibas.ch
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Petr Hrúz, Prof. Dr.
Organizational Affiliation
Clarunis University Center for Gastrointestinal and Liver Diseases
Official's Role
Principal Investigator
Facility Information:
Facility Name
Clarunis University Center for Gastrointestinal and Liver Diseases
City
Basel
ZIP/Postal Code
4002
Country
Switzerland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Petr Hrúz, Prof. Dr.
Phone
0041 61 77 77 575
Email
petr.hruz@clarunis.ch
First Name & Middle Initial & Last Name & Degree
Jean-Pierre Rothen, Dr.
Phone
0041 61 207 61 75
Email
jp.rothen@unibas.ch

12. IPD Sharing Statement

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Cholecalciferol in Chronic Inflammatory Bowel Diseases

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