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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02159144
Other study ID # 2014Wze088
Secondary ID
Status Completed
Phase N/A
First received May 31, 2014
Last updated August 11, 2015
Start date June 2014
Est. completion date September 2014

Study information

Verified date August 2015
Source Wuhan General Hospital of Guangzhou Military Command
Contact n/a
Is FDA regulated No
Health authority China: the ethic committee of Wuhan General Hospital
Study type Interventional

Clinical Trial Summary

Adipose tissues, which include white adipose tissue (WAT) and brown adipose tissue (BAT), play an essential role in regulating whole-body energy homeostasis. Recent studies also reveal the presence of a subset of cells in WAT that could be induced by environmental or hormonal factors to become ''brown-like'' cells, and this ''beigeing'' process has been suggested to have strong antiobesity and antidiabetic benefits. More recently, same studies showed that cold stress stimulate the browning of subcutaneous white adipose. However, to the investigators knowledge, there are no direct data that clearly show that cold stress can promote the browning of subcutaneous white adipose.


Description:

Individuals have cold exposure at 15C for 2 hr everyday for one week.Biopsy for subcutaneous white adipose was performed before and after one week cold exposure programme under local anesthesia. Measure the brown fat characteristics of biopsy samples. The expression levels of uncoupling protein-1 (UCP-1), peroxisome proliferator-activated receptor (PPAR)-r, peroxisome proliferator-activated receptor r coactivator 1 a (PGC1a) , growth factor receptor binding protein-10 (Grb10), PR domain containing 16 (PRDM16) will be determined before and after cold stress programme from the biopsy samples. In addition, a combination of PET and computed tomography (CT) — with the glucose analogue 18F-fluorodeoxyglucose (18F-FDG) as a tracer will be performed for brown adipose tissue before and after cold stress programme.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date September 2014
Est. primary completion date September 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 20 Years to 60 Years
Eligibility Inclusion Criteria:

- healthy men

- 18-60 years old

- BMI 20-28 kg/m2

Exclusion Criteria:

- BMI < 20 kg/m2

- BMI > 28 KG/M2

- Female

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label


Related Conditions & MeSH terms


Intervention

Other:
cold stress


Locations

Country Name City State
China Wuhan General Hospital Wuhan Hubei

Sponsors (1)

Lead Sponsor Collaborator
Xiang Guang-da

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary browning of subcutaneous white adipose Brown fat characteristics of biopsy samples will be assessed by determining the expression levels of UCP1, PGC1a, PRDM16 and Grb10. 4 months No
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