Status:

COMPLETED

Xinju Xiaogao Prescription Study on Overweight

Lead Sponsor:

Guang'anmen Hospital of China Academy of Chinese Medical Sciences

Collaborating Sponsors:

China-Japan Friendship Hospital

The Affiliated Hospital of the Chinese Academy of Military Medical Sciences

Conditions:

Overweight

Eligibility:

All Genders

18-60 years

Phase:

NA

Brief Summary

Xinju Xiaogao prescription and 10% of it in the treatment of adiposity (stagnation of QI causing phlegm retention)clinical study

Detailed Description

Charged by the three research centers in line with traditional Chinese medicine stagnation of QI causing phlegm retention 120 cases have diabetes were randomly divided into Chinese herbal compound Xin...

Eligibility Criteria

Inclusion

  • Aged 18-60 years old
  • BMI≥28kg/m2,but\<40kg/m2
  • Waistline≥85cm(male),≥80cm(female)
  • Pathoglycemia must fulfill one of those four condition:
  • IGT,7.8≤2hPG≤11.0mmol/,
  • diabetics take medicine used to treat type 2 diabetes more than 3 month,and 5.6≤FBG≤12.2,and weight change under 4kg.
  • stagnation of QI causing phlegm retention
  • To sign informed consent.

Exclusion

  • After 3-6 months simply controlling their diet and more exercise treatment, body weight weight loss ≥ 5%.
  • TG\>4.5mmol/L.
  • Suffering from congenital heart disease, rheumatic heart disease, kidney disease, serious active liver disease, peptic ulcer disease or malabsorption syndrome.
  • There is a history of pancreatitis or endocrine diseases other than diabetes, diabetes treated with insulin.
  • Not suffered myocardial infarction in Past 3 months or unstable angina were confirmed.
  • Had been diagnosed as "post-surgical adhesions" .
  • There is a history of appetite or abuse of laxatives
  • Diastolic blood pressure,uncontrolled or controlled, three times greater than 105mmHg .
  • Pregnancy, prepare to pregnant or lactating women prepare.
  • Allergies to Chinese medicine , allergic.
  • Recurrent gallstone or a history of kidney stones.
  • Mentally ill.
  • Cancer patients.
  • A history of gastrointestinal surgery to lose weight.
  • Receiving other clinical studies nearly 3 months.
  • Alcohol and / or psychoactive substances, drug abusers and addicts.
  • Taking other weight-reducing aid Close within one month

Key Trial Info

Start Date :

June 1 2010

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

March 1 2011

Estimated Enrollment :

140 Patients enrolled

Trial Details

Trial ID

NCT01142076

Start Date

June 1 2010

End Date

March 1 2011

Last Update

December 11 2013

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