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Exploring the Effects of Caltrate Supplement on the Chronic Course of Crohn's Disease Patients With Vitamin D Deficiency

Primary Purpose

Crohn's Disease, Vitamin D Deficiency, Vitamin D Supplement

Status
Unknown status
Phase
Early Phase 1
Locations
China
Study Type
Interventional
Intervention
Caltrate Pill
Sponsored by
Second Affiliated Hospital of Wenzhou Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Crohn's Disease

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Clearly diagnosed patients with CD
  • Vitamin D deficiency (<= 20ng / ml)

Exclusion Criteria:

  • Pregnancy, lactation
  • Liver and kidney insufficiency
  • Co-morbid with other autoimmune diseases
  • Use antiepileptic drugs or drugs metabolized by liver cytochrome P450 enzymes
  • Vitamin D level is normal or high

Sites / Locations

  • SAHWenzhouMU

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Caltrate

Control

Arm Description

This group of patients are going to supplemented with Caltrate 0.6 g / d orally.

The other group do not interfere.

Outcomes

Primary Outcome Measures

Serum 25 (OH) D level
Because serum 25 (OH) D levels are relatively stable, they are considered the most reliable indicator of vitamin D status.

Secondary Outcome Measures

White blood cell count
White blood cell count can be used to reflect the degree of inflammation in the body
erythrocyte sedimentation rate
ESR can be used to reflect the degree of inflammation in the body.
C-reactive protein.
C-reactive protein can be used to reflect the degree of inflammation in the human body

Full Information

First Posted
February 17, 2020
Last Updated
October 9, 2020
Sponsor
Second Affiliated Hospital of Wenzhou Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT04276636
Brief Title
Exploring the Effects of Caltrate Supplement on the Chronic Course of Crohn's Disease Patients With Vitamin D Deficiency
Official Title
Exploring the Effects of Caltrate Supplement on the Chronic Course of Crohn's Disease Patients With Vitamin D Deficiency,a Prospective Cohort Study
Study Type
Interventional

2. Study Status

Record Verification Date
October 2020
Overall Recruitment Status
Unknown status
Study Start Date
October 2020 (Anticipated)
Primary Completion Date
March 2021 (Anticipated)
Study Completion Date
March 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Second Affiliated Hospital of Wenzhou Medical University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Aims:Prospectively observe the effects of Caltrate supplementation on the chronic course of Crohn's disease patients, analyze whether the effect of Caltrate on CD patients is affected by factors such as disease site, disease activity, treatment, etc.Provide a certain theoretical basis for "precision treatment" for CD patients in the future. Design:It is a prospective cohort study. Investigators include a total of 60 participants with CD according to the inclusion and exclusion criteria, and divide them into two groups to assess their initial disease activity and detect related indicators. At the same time,Investigators detect the Vitamin D Gene gene polymorphisms in all participants.One group is given Caltrate 0.6g per day orally, and the control group do not intervene. After 12 months, re-evaluate the disease activity and retest the relevant indicators, and use statistical methods to analyze whether Caltrate supplementation treatment can increase the serum 25 (OH) D level of CD participants, improve the condition of CD participants,relationship with Vitamin D Gene Polymorphism,and analyze the effect of Caltrate on participants with CD is affected by factors such as disease site, disease activity, and treatment.
Detailed Description
The research can be started only after approval by the Medical Ethics Committee of the Second Affiliated Hospital of Wenzhou Medical University. According to the "Consensus on Diagnosis and Treatment of Inflammatory Bowel Disease" formulated by the Beijing Conference in 2018 as a standard, patients with clear diagnosis of CD are collected. Exclusion criteria included pregnancy, breastfeeding, liver and kidney dysfunction, concurrent autoimmune diseases, and use of antiepileptic drugs or drugs metabolized by liver cytochrome P450 enzymes. Assess disease activity of CD participants based on the "Simplified Crohn's disease Activity Score". General information about participants with CD is collected. Detection of VDR gene polymorphisms using Snapshot technology. Serum C-reactive protein, erythrocyte sedimentation rate, white blood cells, albumin, creatinine, alanine aminotransferase, calcium and phosphorus levels are measured. The level of serum 25 (OH) D of participants is detected. Develop a treatment plan for participants. Participants are divided into two groups, one group is given oral Caltrate 0.6g / d, and the other group did not intervene. The above serum indicators are re-measured in the 12th month, and the condition of CD participants is also evaluated. Follow-up for 12 months. By comparing the above indicators, observe that in the Han population: Can Caltrate supplementation increase serum 25 (OH) D levels in patients with CD? Can Caltrate supplementation improve the condition of patients with CD? whether vitamin D gene polymorphisms affect the efficacy of Caltrate supplementation therapy? Analyze whether the effect of Caltrate on CD patients is affected by factors such as disease site, disease activity, treatment, etc .. Through statistical analysis, comprehensive analysis of the effectiveness and safety of Caltrate supplementation in Han patients with CD, and its relationship with vitamin D gene polymorphisms, providing a theoretical basis for further "precise treatment" intervention in inflammatory bowel disease.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Crohn's Disease, Vitamin D Deficiency, Vitamin D Supplement

7. Study Design

Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Caltrate
Arm Type
Experimental
Arm Description
This group of patients are going to supplemented with Caltrate 0.6 g / d orally.
Arm Title
Control
Arm Type
No Intervention
Arm Description
The other group do not interfere.
Intervention Type
Drug
Intervention Name(s)
Caltrate Pill
Intervention Description
Vitamin D-deficient CD patients are divided into two groups, one group is given orally with Caltrate Pill 0.6 g / d, while the other group do not interfere.
Primary Outcome Measure Information:
Title
Serum 25 (OH) D level
Description
Because serum 25 (OH) D levels are relatively stable, they are considered the most reliable indicator of vitamin D status.
Time Frame
1year
Secondary Outcome Measure Information:
Title
White blood cell count
Description
White blood cell count can be used to reflect the degree of inflammation in the body
Time Frame
1year
Title
erythrocyte sedimentation rate
Description
ESR can be used to reflect the degree of inflammation in the body.
Time Frame
1year
Title
C-reactive protein.
Description
C-reactive protein can be used to reflect the degree of inflammation in the human body
Time Frame
1year

10. Eligibility

Sex
All
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Clearly diagnosed patients with CD Vitamin D deficiency (<= 20ng / ml) Exclusion Criteria: Pregnancy, lactation Liver and kidney insufficiency Co-morbid with other autoimmune diseases Use antiepileptic drugs or drugs metabolized by liver cytochrome P450 enzymes Vitamin D level is normal or high
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xia sheng long, Master
Phone
0086-15868532956
Email
xsl1989@foxmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xia Xia long, Master
Organizational Affiliation
Second Affiliated Hospital of Wenzhou Medical University
Official's Role
Principal Investigator
Facility Information:
Facility Name
SAHWenzhouMU
City
Wenzhou
State/Province
Zhejiang
ZIP/Postal Code
325000
Country
China

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
Data sets will be made available on relevant requests and in accordance with journal guidelines when publishing results from this study.

Learn more about this trial

Exploring the Effects of Caltrate Supplement on the Chronic Course of Crohn's Disease Patients With Vitamin D Deficiency

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