EUCTR2008-000370-20-IT
Active, not recruiting
Not Applicable
Evaluation of pharmacokinetic and pharmacodynamic interactions between escitalopram and drugs used for the treatment of bipolar disorders. - ND
AZIENDA OSPEDALIERA PISANA0 sitesJuly 1, 2008
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- bipolar disorders
- Sponsor
- AZIENDA OSPEDALIERA PISANA
- Status
- Active, not recruiting
- Last Updated
- 14 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Male and female patients Age between 18 and 70 years Patients candidate to receive escitalopram for major depressive episodes, depressive episodes, panic, anxiety or obsessive\-compulsive symptoms. Patients treated with: lamotrigine, valproic acid, carbamazepine, oxcarbazepine, gabapentin, levetiracetam, and lithium. Those drugs will be prescribed and administered at doses indicated. Patients with adequate bone marrow, liver and renal function. Patients able to provide a Written Informed Consent.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1\.2 Adults (18\-64 years) yes
- •F.1\.2\.1 Number of subjects for this age range
- •F.1\.3 Elderly (\>\=65 years) yes
- •F.1\.3\.1 Number of subjects for this age range
Exclusion Criteria
- •Patients younger than 18 or older than 70 years Patients treated with antipsychotics. Patients need to be treated with antidepressant other than study drug. Patients who will not be able to attend the follow up visits Patients with poor compliance Patients who scored ≥2 at item 3 on HAMD Pregnancy or breast feeding Premenopausal female patients who do not use contraceptives Substance abuse or dependence within the last year A diagnosis of renal or liver failure, jaundice, cardiopathy or severe lung diseases, hematological diseases and past episodes of photosensibilization.
Outcomes
Primary Outcomes
Not specified
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