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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 19 February 2015
Main ID:  NCT01349387
Date of registration: 03/05/2011
Prospective Registration: No
Primary sponsor: Centre d’Etudes et de Recherche pour l’Intensification du Traitement du Diabète
Public title: Effect of Treatment With Metformin in Type 2 Diabetes Patients on Alternative Genes Splicing METFORGENE
Scientific title: Effect of Treatment With Metformin in Type 2 Diabetes Patients on Alternative Genes Splicing Whose Maturation Depends on the Protein HuR, Including Gene Encoding Insulin Receptor
Date of first enrolment: May 2011
Target sample size: 25
Recruitment status: Completed
URL:  http://clinicaltrials.gov/show/NCT01349387
Study type:  Interventional
Study design:  Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Basic Science  
Phase:  N/A
Countries of recruitment
France
Contacts
Name:     Guillaume CHARPENTIER, MD
Address: 
Telephone:
Email:
Affiliation:  CHSF-CERITD
Key inclusion & exclusion criteria

Inclusion Criteria:

- Type 2 Diabetic patients usually treated with metformin (= 1400 mg/day), associated
or not to other oral anti-diabetic treatment or. injection treatment

- Patients major.

- Patients with a social security number

- Patients having signed a consent to participate in the study

Exclusion Criteria:

- Intolerance metformin

- Patients with type 1.

- Patients on pioglitazone or rosiglitazone

- Renal failure by an anomaly of the creatinine clearance (< 60 mL/min).

- Patients pregnant or likely to be.



Age minimum: 18 Years
Age maximum: N/A
Gender: Both
Health Condition(s) or Problem(s) studied
Type 2 Diabetes
Intervention(s)
Drug: Metformin
Primary Outcome(s)
Comparison of expression of isoforms A and B of the insulin receptor using quantitative RT PCR [Time Frame: inclusion (baseline), 30th days and 60th days]
Secondary Outcome(s)
Secondary ID(s)
2010-A01389-30
2011-000128-13
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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