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临床试验/NCT04868227
NCT04868227已完成不适用

Scottish Vitamin D Intervention Study

University of Edinburgh2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2014年3月28日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
50
试验地点
2
主要终点
Number of Genes Significantly Associated With 25OHD Blood Vitamin D Level

研究概览

简要总结

AIMS To identify the underlying mechanism by which Vitamin D reduces colorectal cancer risk.

OBJECTIVES To demonstrate the effects of vitamin D supplementation on serum vitamin D levels.

To demonstrate dynamic changes in gene expression in response to vitamin D. To demonstrate the mechanism underlying the gene-environment interaction of vitamin D, susceptibility genetic variants (risk genes) and colorectal cancer.

详细描述

Through National Health Service (NHS) clinical services in colorectal surgery and oncology, patients will be identified and recruited from surgical wards or surgical/oncology out-patient clinics. A sample of participants with and without a new or previous diagnosis of colorectal cancer will be included for comparison.

Participation will consist of two events in the majority of participants. Firstly a in the surgical ward or clinic lasting no longer than 20 minutes in which the research will be discussed and informed consent gained. A blood sample will be taken prior to the conclusion of recruitment and a rectal biopsy taken using a rigid sigmoidoscopy which may or may not be required as part of their routine clinical assessment. Participants will be asked to take pharmaceutical grade vitamin D tablets for 3 months. After 12 weeks of vitamin D supplementation, a final blood sample and rectal biopsy will be taken.

If patients would like to contribute but cannot or would prefer not to take vitamin D, or cannot return for future sampling, a single sampling will be offered. This participant would undergo blood sampling and rectal biopsy as above. After this no further events would occur.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Aged 16 years or over.
  • Resident of the United Kingdom

排除标准

  • The inability to provide informed consent.
  • Under the age of 16 years.
  • A non-UK resident.
  • Patients who may be at increased risk from rigid sigmoidoscopy:
  • Individuals who are taking anti-coagulation medication.
  • Individuals with platelet disease or other bleeding issues.
  • Individuals with a history of a significant rectal bleed.
  • Suspected or known bowel perforation
  • Anal stenosis
  • Acute peritonitis
  • Colonic necrosis
  • Toxic megacolon
  • Acute severe diverticulitis
  • Diverticular abscess
  • Recent colonic surgery
  • Anal fissure
  • Severe coagulopathy
  • Anticoagulant therapy
  • Severe thrombocytopenia
  • Severe neutropenia
  • Patients who may be at increased risk from Vitamin D supplementation would not be included in the intervention arm but could still be included in the single sample arm:
  • Kidney disease
  • High levels of calcium in the blood
  • Atherosclerosis
  • Sarcoidosis
  • Histoplasmosis
  • Over-active parathyroid gland (hyperparathyroidism)
  • Currently taking thiazide diuretics, digoxin or other cardiac glycosides
  • Known allergy to nuts ( as peanut oil contained within vitamin D preparations)
  • Female subjects of child bearing age who are not taking effective contraception during the period of the trial
  • Patients in whom vitamin D levels may be unpredictable
  • Individuals already established on supplementary Vitamin D.
  • Individuals recently returned to the UK from an overseas holiday.
  • Individuals who have recently lived abroad.
  • Patients on anti-epileptic medication

结局指标

主要结局

Number of Genes Significantly Associated With 25OHD Blood Vitamin D Level

时间窗: AT BASELINE

RECTAL MUCOSA GENE EXPRESSION (HT12 microarray. No units on gene expression array)

GENE EXPRESSION CHANGE

时间窗: AFTER 12 WEEK'S SUPPLEMENTATION

RECTAL MUCOSA GENE EXPRESSION. We tested supplemented patients (i.e. response to supplementation) for enrichment of the candidate gene-set. Directional gene-set testing was performed in R, using the gene-setTest function in the 'limma' package. We performed participant-level gene-set enrichment testing with a 'response' to supplementation defined as enrichment (P\<0.001) of the candidate gene-set after supplementation.

次要结局

  • VITAMIN D STATUS(AT BASELINE)
  • VITAMIN D STATUS CHANGE(AFTER 12 WEEK'S SUPPLEMENTATION)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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