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Study ID Status Title Patient Level Data
29060/257 Completed An Open Multicentre Study to Assess the Safety and Efficacy of Paroxetine in Patients with Depression
29060/258 Completed An Early Clinical Phase II Evaluation of Paroxetine, a New Product and 5-HT Uptake Inhibitor in Patients with Depressive Illness
29060/259 Completed Paroxetine, a Selective Serotonin Uptake Inhibitor in the Treatment of Depressive Illness – a Clinical Phase II Study
29060/260 Completed Paroxetine in the treatment of depression – a randomised comparison with amitriptyline.
29060/261 Completed A Double-Blind, Comparative Study of Paroxetine and Clomipramine to Assess Efficacy and to Evaluate the Correlation Between Plasma Concentration and Effect
29060/268 Completed A study to assess the efficacy and safety of paroxetine in patients with depression
29060/270 Completed Comparison of the effects of single doses of paroxetine, amitriptyline and placebo on systolic time intervals in volunteers
29060/272 Completed A Comparison of the Efficacy and Tolerance of Paroxetine and Amitriptyline in the Treatment of Depression. A Double-Blind, Parallel Study
29060/274 Completed A study to assess the effectiveness and tolerance of paroxetine by double-blind comparison with placebo Study Listed on ClinicalStudyDataRequest.com
29060/276 Completed A double-blind study to investigate the efficacy, safety and tolerability of Paroxetine in the treatment of depression in comparison with placebo Study Listed on ClinicalStudyDataRequest.com
29060/277 Completed The effect of paroxetine taken in the evening, on sleep in human non-depressed, poor sleepers
29060/278 Completed The effect of paroxetine taken in the morning on sleep in human non-depressed, poor sleepers
29060/281 Completed A trial to assess the effectiveness and tolerance of paroxetine by double-blind comparison with amitriptyline in the treatment of depressed patients in General Practice
29060/282 Completed A trial to assess the effectiveness and tolerance of paroxetine by double-blind comparison with placebo using a novel “shifted crossover” design Study Listed on ClinicalStudyDataRequest.com
29060/283/014B Completed The Short Term Phase of an Open, Long-Term, Safety and Tolerability Study of Paroxetine in Patients Suffering from Depression
29060/284 Completed A comparison of the effect of paroxetine and amitriptyline in single doses on psychomotor performance
29060/285 Completed To assess the effect of repeated dosing with paroxetine, amitriptyline and placebo on psychomotor skills and cardiac function in volunteers
29060/286 Completed An investigation of the pharmacokinetics, efficacy, and tolerance of paroxetine in geriatric patients with depression
29060/287 Completed A Report on the Short-Term Phase of an Open Long-Term Study to Investigate the Safety of Paroxetine in Geriatric Patients
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.

 

 

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GSK-sponsored clinical studies 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.
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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