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Study ID Status Title Patient Level Data
29060/421 Completed Paroxetine and Fluoxetine effects on mood and cognitive function in depressed nondemented elderly patients. Extensive searching has revealed that no clinical report is available for this study. The clinical trial results were reported via publications; see citation below.
29060/427 Completed A Multicentre, Double-Blind, Placebo-Controlled Study to Investigate the Effects of Paroxetine (5mg OD Vs 10mg OD Vs 20mg OD) in Patients with Premenstrual Dysphoric Disorder (PMDD).
29060/433 Completed Treatment of fibromyalgia: a randomized, double-blind, placebo-controlled study of paroxetine, a selective serotonin re-uptake inhibitor
29060/436 Completed Safety Evaluation of Paroxetine in Elderly Depressed Patients
29060/437 Completed A Double-blind, Placebo-controlled Study to Investigate the Effect of Pindolol on the Onset of Anti-depressant Activity of Paroxetine in the Treatment of Depression.
29060/440 Completed A single dose 4-part crossover study to determine the comparative bioavailability of an oral liquid formulation of paroxetine (20 mg pfb) and a standard 20 mg pfb Paxil tablet administered immediately before and after breakfast
29060/442 Completed A multicentre, randomised, double-blind study to compare paroxetine versus placebo in the treatment of double depression.
29060/448 Completed A Double-Blind, Placebo Controlled Trial to Evaluate the Clinical Effects of Immediate Release Paroxetine and Modified Release Paroxetine in the Treatment of Major Depression Study Listed on ClinicalStudyDataRequest.com
29060/449 Completed A Double-Blind, Placebo Controlled Trial to Evaluate the Clinical Effects of Immediate Release Paroxetine and Modified Release Paroxetine in the Treatment of Major Depression Study Listed on ClinicalStudyDataRequest.com
29060/451 Completed An open 5 part crossover study to examine the bioavailability characteristics of two controlled-release and two delayed-release oral formulations of paroxetine (20 mg), in comparison with a standard 20 mg tablet, in healthy volunteers
29060/452 Completed A double-blind, placebo-controlled, parallel group study to investigate the incidence of nausea following 3 days treatment with modified release formulations of paroxetine compared with the standard immediate release paroxetine tablet at a dose level of 30 mg in healthy volunteers
29060/453 Completed A 38-Week, Two Phase, Multi-center Study to Investigate the Safety and Effectiveness of paroxetine (10-60mg/day in the Treatment of Children and Adolescent Outpatients with Obsessive Compulsive Disorder (OCD)
29060/454 Completed A Randomized, Double-Blind, Fixed Dose Comparison of 20, 40, and 60mg Daily of Paroxetine and Placebo in the Treatment of Generalized Social Phobia. Study Listed on ClinicalStudyDataRequest.com
29060/464 Completed Bioequivalence study of paroxetine hydrochloride formulations: bioequivalence study between two paroxetine hydrochloride 20 mg tablets of different formulas (new and old formula tablets) in healthy adult volunteers
29060/470 Completed An Extension Trial Comparing Paroxetine and Placebo in the Long Term Treatment of Generalized Social Phobia
29060/472 Completed A randomised, open, four-period crossover study to compare the pharmacokinetic profile of paroxetine after single doses of each enteric coated Geomatrix controlled-release tablet strength (12.5, 25, 37.5 and 50 mg)
29060/473 Completed A single dose, two-period crossover study to compare the bioavailability of paroxetine from the enteric-coated Geomatrix controlled-release paroxetine tablet (50 mg) when administered in the fasted state and after a standard FDA high-fat breakfast
29060/474 Completed A steady-state, two-period crossover study to compare the pharmacokinetic profile of paroxetine after repeated daily dosing of the controlled release paroxetine tablet (50 mg) with that of standard immediate release paroxetine (Paxil, 40 mg)
29060/475 Completed Pharmacokinetic study of paroxetine hydrochloridePharmacokinetics after single oral administration of paroxetine hydrochloride 20 mg to healthy elderly volunteers
29060/480 Completed A single-dose, two-period crossover study to demonstrate bioequivalence between the controlled-release paroxetine tablet (50 mg) manufactured at Cidra and two 25 mg controlled-release tablets manufactured at Crawley
29060/485 Completed An open 3 part crossover study to examine the bioavailability characteristics of slow release oral formulations of paroxetine (30 mg dose), in comparison with a standard, immediate release 30 mg tablet, in healthy volunteers
29060/486 Completed The effects of paroxetine on the pharmacodynamics and pharmacokinetics of terfenadine in healthy adult males
29060/487 Completed A Double-Blind, Placebo Controlled Trial to Evaluate the Clinical Effects of Immediate Release Paroxetine and Controlled Release Paroxetine in the Treatment of Major Depression in Elderly Patients Study Listed on ClinicalStudyDataRequest.com
29060/494 Completed A Double-Blind, Placebo-Controlled, Flexible-Dosing Trial to Evaluate the Efficacy of Modified-Release Paroxetine in the Treatment of Panic Disorder Study Listed on ClinicalStudyDataRequest.com
29060/495 Completed A Double-Blind, Placebo-Controlled, Flexible-Dosing Trial to Evaluate the Efficacy of Controlled-Release Paroxetine in the Treatment of Panic Disorder 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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