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Study ID Status Title Patient Level Data
29060/289 Completed A Study to Assess the Efficacy and Tolerance of Paroxetine in Patients with Depression by Double-Blind Comparison with Clomipramine
29060/290 Completed A prospective, randomized, double-blind, multicentre study of the efficacy and tolerance of paroxetine versus clomipramine in the treatment of endogenous depression in the elderly
29060/291 Completed A Multi-Centre Double-Blind Study to Investigate the Safety and Efficacy of Paroxetine in Comparison with Clomipramine in the Treatment of Reactive Depression in Elderly Patients.
29060/292 Completed A multi-centre study to assess the effectiveness and tolerance of paroxetine by double-blind comparison with amitriptyline
29060/294 Completed A study to investigate the effects of food on the bioavailability of a single 20 mg dose of ‘Paxil’ (paroxetine) in healthy volunteers
29060/298 Completed A double-blind study comparing the efficacy and tolerability of paroxetine and placebo in hospital out-patients with depressive symptoms associated with chronic back pain.
29060/299 Completed A Double-Blind Study Comparing The Efficacy and Tolerability of Paroxetine and Amitriptyline In Patients With Severe Depression.
29060/303 Completed A double blind, placebo controlled study to determine the effects of subchronic paroxetine treatment on nocturnal hormonal secretion and sleep in healthy male volunteers
29060/308 Completed Early clinical evaluation of a new antidepressant: A double-blind parallel study comparing paroxetine 30mg daily with amitriptyline 150mg daily
29060/309 Completed Early Clinical Evaluation of a New Antidepressant: A Double-Blind Parallel Study Comparing Paroxetine 30mg Daily with Amitriptyline 100mg Daily
29060/310 Completed Early Clinical Evaluation of a New Antidepressant: Double-Blind Parallel Study Comparing Paroxetine 30mg Daily with Amitriptyline 150mg Daily
29060/311 Completed Early clinical evaluation of a new antidepressant: An open pilot study of paroxetine 40mg daily
29060/312 Completed A Phase II Pharmacokinetic Double Blind Study Comparing Paroxetine with Amitriptyline in Depressed Patients
29060/313 Completed A study to assess the efficacy and pharmacokinetics of paroxetine in depressed geriatric patients
29060/314 Completed Double Blind Parallel Study Comparing Paroxetine, 30mg Daily, and Amitriptyline, 150mg Daily, in Depressed Patients
29060/315 Completed Early clinical evaluation of a new antidepressant: An open pilot study of paroxetine 40mg daily
29060/316 Completed Early Clinical Evaluation of a New Antidepressant: A Double-Blind Parallel Study Comparing Paroxetine 30mg Daily with Amitriptyline 150mg Daily
29060/317 Completed An early clinical evaluation of a new antidepressant: An open study of paroxetine 40mg o.d.
29060/318 Completed Early Clinical Evaluation of a New Antidepressant: A Double-Blind Parallel Study Comparing Paroxetine 30mg Daily with Amitriptyline 150mg Daily
29060/319 Completed Early clinical evaluation of a new antidepressant: A double-blind parallel study comparing paroxetine 30mg daily, with amitriptyline 150mg daily.
29060/320 Completed An open labelled study to investigate the safety and tolerability of paroxetine when single oral dosing of 40 mg of paroxetine in healthy volunteers
29060/322 Completed Phase I clinical investigation of paroxetine. The pharmacokinetics, safety and tolerance of single and repeat oral administration of paroxetine in healthy volunteers
29060/326 Completed A double-blind, randomised multi centre study to assess the safety and tolerability of paroxetine and amitriptyline in depressed subjects stabilised on lithium treatment
29060/327 Completed A double-blind, placebo-controlled, parallel group study of paroxetine in the treatment of dysthymia. Study Listed on ClinicalStudyDataRequest.com
29060/329 Completed A Multi-center, Double-blind, Placebo-Controlled Study of Paroxetine and Imipramine in Adolescents with Unipolar Major Depression - Acute Phase Study Listed on ClinicalStudyDataRequest.com

 

 

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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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