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Vitamin D Supplementation to Obese Chinese Males

S

Shenzhen Center for Chronic Disease Control

Status

Completed

Conditions

Insulin Resistance
Obesity

Treatments

Dietary Supplement: Oral supplementation of vitamin D

Study type

Interventional

Funder types

Other

Identifiers

NCT01781169
VD50kIU2011

Details and patient eligibility

About

Hypothesis: Oral Supplementation of Vitamin D can Reduce Hypersecretion of Parathyroid Hormone and Insulin Resistance in Obese Chinese Males.

Protocol: Weekly oral supplementation of 50,000 IU vitamin D (cholecalciferol) or eight weeks to the obese males compared with the normal-weight males. Index measures were conducted at baseline and endpoint.

Enrollment

43 patients

Sex

Male

Ages

23 to 66 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • body mass index (BMI) ≥ 28kg/m2 or 18.5 ≤ BMI < 24 (kg/m2)
  • non vegetarian Han Chinese and did not smoke, drink, nor take vitamin D supplements for > 2 y
  • fasting serum glucose < 7.0 mmol/L
  • serum glucose of 2 hr after 75 g oral glucose loading < 11.1 mmol/L
  • normal functioning of liver and kidney evaluated by alkaline phosphatase, aspartate aminotransferase, creatinine, and uric acid

Exclusion criteria

  • not match the above inclusion criteria
  • diagnosed as having any organic diseases were excluded

Trial design

Primary purpose

Health Services Research

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

43 participants in 2 patient groups

Obese group
Experimental group
Description:
Oral supplementation of vitamin D (cholecalciferol), 50000 IU/wk for 8 weeks.
Treatment:
Dietary Supplement: Oral supplementation of vitamin D
Normal-weight group
Experimental group
Description:
Oral supplementation of vitamin D (cholecalciferol), 50000 IU/wk for 8 weeks.
Treatment:
Dietary Supplement: Oral supplementation of vitamin D

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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