Phase
Condition
Joint Injuries
Rheumatoid Arthritis
Treatment
Placebo
Methotrexate treatment
Metformin treatment
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Patients aged over 18 years old,
Patient affected by RA according to American College of Rheumatology (ACR) 2010criteria
DAS28-ESR > 3.2
Methotrexate naïve patients, or without any methotrexate intake for more than sixmonths.
Men who accept to take active contraception during the study and during six monthsafter the end of the Methotrexate treatment. Partner of patient will be informed ofteratogenicity of MTX and will be advised to be on effective contraceptives for allthe study duration.
OR
Women with a negative test of β-human chorionic gonadotropin (HCG) who accept totake active contraception during the study and during six months after the end ofthe Methotrexate treatment
Patients without any Metformin previous therapy.
Being affiliated to a health insurance system
Having signed an informed consent form (later than the day of inclusion and beforeany examination required by the research)
Exclusion
Exclusion Criteria:
Patient who present contraindications to treatment with Methotrexate or Metformin
Patient with type 1 or type 2 diabetes
Patient with daily corticosteroid treatment at a dosage ≥ 15 mg/day within fourweeks before the inclusion
History of allergy or intolerance to biguanide
Presence of anemia (hemoglobin < 80 g/l), neutropenia (neutrophils count < 1500mm3), lymphopenia (lymphocytes count < 750 mm3), thrombopenia (platelets < 100 000/mm3) or bone marrow hypoplasia.
Renal insufficiency with clearance < 50 ml/mn
Decompensated heart failure
Uncontrolled heart history
Severe respiratory insufficiency
Hepatic insufficiency, or bilirubin level upper than 5mg/dl (85,5 µmol/l), oraspartate transaminase (ASAT) / alanine aminotransferase (ALAT) more than twice thestandard level.
Acute or chronic infection, such as tuberculosis or HIV
Critical ischemia of the lower limbs
Recent stroke
Patient with pleural effusion, or ascites
Patient with stomatitis, mouth ulcers, or active gastrointestinal ulcer.
Patient with alcohol intoxication
B12 Vitamin deficiency
Patient performing or planning to perform a long-fasting period
Pregnant or breastfeeding women
Patient concerned by articles L 1121-5 to L 1121-8 (persons deprived of theirliberty by a judicial or administrative decision, minors, persons of legal age whoare the object of a legal protection measure or unable to express their consent).
Study Design
Study Description
Connect with a study center
CH de la Côte Basque - service de rhumatologie
Bayonne,
FranceSite Not Available
CHU de Bordeaux - service de rhumatologie
Bordeaux,
FranceSite Not Available
CHU de Brest - service de rhumatologie
Brest,
FranceSite Not Available
CH de Cahors - service de rhumatologie
Cahors,
FranceSite Not Available
Clinique de l'Infirmerie protestante de Lyon - service de rhumatologie
Caluire-et-Cuire,
FranceSite Not Available
CHD de Vendée - service de rhumatologie
La Roche-sur-Yon,
FranceSite Not Available
CH du Mans - service de rhumatologie
Le Mans,
FranceSite Not Available
CH de Libourne - service de rhumatologie
Libourne,
FranceSite Not Available
CHU de Limoges - service de rhumatologie
Limoges,
FranceSite Not Available
CHU de Montpellier - service de rhumatologie
Montpellier,
FranceSite Not Available
CH des Pays de Morlaix - service de rhumatologie
Morlaix,
FranceSite Not Available
CHR Orléans la Source - service de rhumatologie
Orléans,
FranceSite Not Available
CH de Pau - service de rhumatologie
Pau,
FranceSite Not Available
CHU de Toulouse - service de rhumatolgie
Toulouse,
FranceSite Not Available
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