SOLMANIA - Comparison of Valproate-Amisulpride and Valproate-Haloperidol in Bipolar I Patients

NCT ID: NCT00126009

Last Updated: 2008-04-10

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 120 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2004-05-31

Brief Summary

The primary objective is:

• To compare the efficacy of the association valproate-amisulpride (400 to 800 mg/day) to the association valproate-haloperidol (5 to 15 mg/day) in bipolar I patients suffering from a manic episode according to DSM IV TR (American Psychiatric Association [APA] 2000) and treated for a 3-month period.

The secondary objectives are:

• To evaluate the clinical and biological safety of the association valproate-amisulpride to the association valproate-haloperidol;
• To assess the patient status 3 weeks and 3 months after inclusion; and
• To assess patient satisfaction at 3 months.

Conditions

Bipolar Disorder

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Interventions

Amisulpride

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• In-patients
• From 18 to 65 years old
• Able to comply with the protocol
• Having given their written informed consent (with a legal representative or a person of trust)
• Current diagnosis of bipolar I disorder according to DSM IV TR (APA 2000)
• Having had at least one manic episode in the past
• Currently suffering from a manic episode according to DSM IV TR (APA 2000)
• A minimum total score of 20 on the Young Mania Rating Scale (Y-MRS) at D-3

• Having completed at least one day of the one to three-day washout period
• A minimum total score of 20 on the Young Mania Rating Scale at D0
• A score of > or = 3 for 2 of the following Y-MRS items: elevated mood; increased motor activity energy; sleep; content (grandiosity).
• A score of > or = 5 on the Clinical Global Impression Severity Scale for the severity of mania items at D0
• Using an effective contraception method (women of childbearing age only)

Exclusion Criteria

• Having participated in a clinical trial within the three previous months
• Pregnant or breast-feeding. Female patients should therefore be using reliable contraceptive methods (oral or parenteral contraception, intra-uterine device or surgical sterilisation)
• Uncontrolled gastro-intestinal, renal, hepatic, endocrine, cardiovascular, pulmonary, immunological or hematological disease
• Central nervous system (CNS) neoplasm; demyelinating disease; degenerative neurological disorder; active CNS infection; or any progressive disorder that may confound interpretation of the study results
• Prolactin-dependant tumor
• Past or current pancreatitis
• Acute hepatitis, chronic hepatitis, or family history of severe hepatitis, especially drug related, hepatic porphyry
• Current or recent (within 3 months) DSM IV diagnosis of substance dependence (with the exception of nicotine or caffeine dependence); or substance abuse with stimulants including, but not limited to, cocaine, crack, amphetamines, pseudoephedrine, cold medications with phenylephrine, or other stimulants. Alcohol and marijuana abuse prior to study entry would be acceptable if related to the current manic episode, based on the investigator's judgement
• Parkinson's disease
• Phaeochromocytoma
• History of epilepsy
• History of allergy or hypersensitivity to haloperidol or benzamides or valproate
• Treated with fluoxetin within the past 4 weeks
• Treated with injectable long-acting neuroleptics if, for the patient, the interval between 2 injection periods has not elapsed before pre-inclusion (D-3)
• Treated with a mood stabiliser (other than valproate) at effective dose for less than 7 days preceding D-3 and for whom a modification is not justified
• Bradycardia < 55 beats per minute (bpm)
• Known hypokaliaemia
• Congenital prolongation of the QT interval
• Treated with any of the following medications: Class Ia antiarrhythmic agents such as quinidine, disopyramide/Class III antiarrhythmic agents such as amiodarone, sotalol; Drugs like: beperidil, cisapride, sultopride, thioridazine, intravenous (IV) erythromycin, IV vincamine, halofantrine, pentamidine, or sparfloxacin.

• Potentially significant alterations of laboratory tests on D0:

• ASAT or ALAT > 2 upper limit of normal (ULN). If ASAT or ALAT values range between 1.5 ULN and 2 ULN, the patient can be randomized and a new test will be performed 7 days after randomization;
• Alkaline phosphatase levels or bilirubin levels not within normal reference range.
• QTc prolongation on D0; QTc Bazett > 450ms in male patients and QTc > 470ms in female patients on electrocardiogram (ECG).

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Sanofi

INDUSTRY

Sponsor Role: lead

Principal Investigators

Gilles Perdriset, MD

Role: STUDY_DIRECTOR

Sanofi

Locations

Sanofi-Aventis

Prague, , Czechia

Sanofi-Aventis

Paris, , France

Sanofi-Aventis

Warsaw, , Poland

Sanofi-Aventis

Bratislava, , Slovakia

Sanofi-Aventis

Barcelona, , Spain

Countries

Czechia; France; Poland; Slovakia; Spain

Other Identifiers

C_8428

Identifier Type: -

Identifier Source: org_study_id