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Study ID Status Title Patient Level Data
29060/329_1 Completed A Multi-center, Double-blind, Placebo-Controlled Study of Paroxetine and Imipramine in Adolescents with Unipolar Major Depression - Continuation Phase. Study Listed on ClinicalStudyDataRequest.com
29060/331 Completed Paroxetine in Depressed Patients with Ischemic Heart Disease- A Randomized Safety Study
29060/332 Completed A Double-Blind, Multicentre Study to Assess the Efficacy and Tolerability of Paroxetine and Amitriptyline in Patients With a Mild, Moderate, or Severe Depressive Episode Associated With Rheumatoid Arthritis
29060/348 Completed Bioequivalence study of paroxetine hydrochloride formulations: bioequivalence study between two paroxetine hydrochloride formulations (10 mg tablet and 20 mg tablet) in healthy adult volunteers
29060/352 Completed A Double-Blind, Placebo-Controlled, Comparison of Imipramine and Paroxetine in the Treatment of Bipolar Depression
29060/353 Completed A Ten-Week, Single-Blind, Multicentre Study Evaluating the Efficacy and Tolerability of Paroxetine vs. Desipramine in the Treatment of Outpatients with Major Depression According to DSM-III-R
29060/356 Completed A double-blind, multicentre study to compare paroxetine and fluoxetine in the treatment of patients with major depressive disorder with regard to antidepressant efficacy, effects on associated anxiety and tolerability.
29060/356_1 Completed Extension phase for a double-blind, multicentre study to compare paroxetine and fluoxetine in the treatment of patients with major depressive disorder with regard to antidepressant efficacy, effects on associated anxiety and tolerability.
29060/358 Completed Comparative study of paroxetine and mianserin in depression of the elderly: efficacy, tolerance, serotonin dependence.
29060/360 Completed A single dose, crossover study to determine the comparative bioavailability of an oral liquid preparation of paroxetine (30 mg pfb) and a 30 mg pfb paroxetine tablet
29060/368 Completed Belgian Paroxetine Experience: An open-label study evaluating the efficacy and safety of paroxetine in depressed patients treated by Belgian psychiatrists and general practitioners
29060/374 Completed A repeat-dose steady-state crossover evaluation of the bioequivalence of a 20 mg “wet granulation” standard Paxil™ tablet with a liquid formulation of paroxetine (20 mg p.f.b)
29060/377 Completed A Double-blind, Multicentre Placebo-Controlled Study of Paroxetine in Adolescents with Unipolar Major Depression. Study Listed on ClinicalStudyDataRequest.com
29060/382 Completed A Randomized, Double-Blind, Comparison of Paroxetine and Placebo in the Treatment of Generalized Social Phobia Study Listed on ClinicalStudyDataRequest.com
29060/391 Completed A double-blind study of the effects of paroxetine, fluoxetine and placebo on driving ability in healthy volunteers
29060/395 Completed Double-blind, randomised study to compare the effects of paroxetine and amitriptyline on driving ability and psychomotor performance in patients with mild to moderate depression treated for at least 4 weeks
29060/397 Completed A double-blind multicentre study to assess the tolerability and efficacy of paroxetine compared with amitriptyline in the treatment of depressed patients in general practice
29060/398 Completed Pharmacokinetics of paroxetine 10 mg, 20 mg and 40 mg in single oral administration in healthy volunteers
29060/400 Completed A Double-Blind, Placebo Controlled Study to Investigate the Efficacy, Safety and Tolerability of Paroxetine in Patients with Premenstrual Dysphoric Disorder.
29060/402 Completed A double-blind, multicentre, parallel group study of paroxetine and amitriptyline in the treatment of patients with depression associated with breast cancer
29060/403 Completed Antidepressant efficacy and safety of paroxetine; a double blind amitriptyline controlled multicenter comparison study in depressive patients.
29060/406 Completed A Double-Blind, Long-Term Extension Study for Patients Previously Participating in Protocol 29060/131
29060/409 Completed A comparative, controlled double blind, double dummy study about the efficacy and safety of paroxetine vs imipramine in ambulatory patients with major depression
29060/418 Completed A single-dose 3-part crossover study to determine the comparative bioavailability of two oral liquid preparations of paroxetine (30 mg pfb) and a 30 mg tablet of paroxetine
29060/419 Completed A repeat-dose steady-state crossover evaluation of the bioequivalence of a 20 mg direct compression tablet of paroxetine with a 20 mg standard “Paxil” tablet

 

 

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GSK-sponsored clinical trials are those for which GSK is ultimately responsible for all aspects of the study even if some or all of these activities are transferred to another party.

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