Overview
Comparative the Effect of Metformin and Acupuncture on Weight Loss and Insulin Sensitivity
Status:
Completed
Completed
Trial end date:
2015-04-01
2015-04-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The investigators designed this randomized double blind (patients/ assessor) clinical trial to compare the therapeutic effects of Metformin monotherapy with Metformin and acupuncture combined therapy on weight loss and insulin sensitivity among overweight/obese type 2 diabetes mellitus (T2DM) patients. We compared the inflammatory markers, lipid profiles, and adipokines in overweight/obese T2DM patients receiving the combined therapy to those receiving the Metformin monotherapy, to understand whether acupuncture plus Metformin is a better approach then Metformin only on treating diabetes.Phase:
N/AAccepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Amir FirouzjaeiTreatments:
Insulin
Metformin
Criteria
Inclusion Criteria:- Who had been diagnosed with type 2 diabetes mellitus and has using Metformin
monotherapy as well to control their diabetes during the period of this study as
previously (500 mg one/two/three times per day)
- All patients were overweight according to BMI ≥25
Exclusion Criteria:
- Individuals with nephritic syndrome (urine protein over 3.5 g/day), edema or renal
failure (serum creatinine over 115 µmol/L)
- Individuals who had been diagnosed with heart failure (NYHA Fc III-IV) or who had been
a pacemaker implanted
- Individuals with abnormal liver dysfunction (GOT and glutamate-pyruvate transaminase
(GPT) levels twofold above the normal range) or a diagnosis of liver cirrhosis
- Individuals with a high HbA1C level (HbA1C above 9 %)
- Pregnant women
- Individuals who were receiving insulin therapy already
- Individuals who receive other therapy or had any change at dosage during the period of
therapy
- Individuals who were suffering from endocrine abnormalities such as Thyroid disease,
polycystic ovary syndrome (PCOS), etc
- Individuals who were receiving weight loss medicine, anti depressant agents' or
hormonal medicines during the last 3 months and the period of study
- Individuals who were suffering from a homeostasis disorder or other systemic disease
- Individuals who did not comply(signed informed consent) with the treatment during the
study period