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Study ID Status Title Patient Level Data
RES106087 Completed A randomized, double-blind study of treatment with a known anti-inflammatory (prednisolone) to evaluate novel endpoints in patients with chronic obstructive pulmonary disease (COPD)
RES11086 Completed Investigation of the side effects of orally administered glucocorticoids. An open label study to investigate the effects of orally administered prednisolone on bone metabolism in patients with COPD.
RH01299 Completed The Effect of Fluoride in an Experimental Dentifrice on Remineralization of Erosive Lesions In-Situ
RH01324 Completed A clinical study investigating the efficacy of a dentifrice in providing short term relief from dentinal hypersensitivity
RH01325 Completed A clinical study investigating the efficacy of a dentifrice in providing long term relief from dentinal hypersensitivity
RH01333 Completed A Randomized, Cross-Over, Single Dose Pharmacokinetic Study of 4mg Nicotine Lozenges.
RH01361 Completed Effects of two doses of a common cold treatment on cognitive function
RH01379 Completed A Single Centre, Examiner-blind Human Patch Test of Bactroban Disinfectant Liquid on Normal Skin
RH01381 Completed In Situ Study to Confirm the Anti-caries Potential of a 1.1365% w/w Sodium Monofluorophosphate (1500ppm F) Dentifrice
RH01390 Completed A Clinical Study to Evaluate Experimental Children's Toothpastes in an In-Situ Caries Model
RH01418 Completed A Pharmacokinetic Evaluation of Two Nicotine Patches in Smokers
RH01426 Completed A Proof of Concept Study to Evaluate the Efficacy of an Occlusion Based Dentifrice in the Relief of Dentinal Hypersensitivity
RH01561 Completed Clinical study to evaluate the efficacy of chlorhexidine mouthwashes
RH01589 Completed A Study to Evaluate Relief of Provoked Acute Craving by Nicotine Mouth Film and Nicotine Lozenge
RH01591 Completed A Proof of Concept Study to Evaluate the Efficacy of an Occlusion Based Dentifrice in the Relief of Dentinal Hypersensitivity
RH01619 Completed A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multi-Center Study to Assess the Efficacy of Once-Daily Fluticasone Propionate Aqueous Nasal Spray 200mcg for 14 Days on Ocular Symptoms Associated with Seasonal Allergic Rhinitis
RH01685 Completed A Clinical Study Investigating the Efficacy of a Dentifrice in Providing Long Term Relief from Dentinal Hypersensitivity
RH01705 Completed A pharmacokinetic study comparing two nicotine gum formulations in a single dose design
RH01899 Completed The effect of a nutritional supplement on post prandial glucose and lipids in an adult population
RH01948 Completed Contac Nasal Spray Questionnaire
RHS00691 Completed Meta-analysis of the efficacy of ranitidine 75mg and ranitidine 150mg versus placebo on the reduction of severity or prevention of meal-induced heartburn
ROF102100 Completed A randomised, double blind, placebo-controlled, parallel group study to investigate the safety and efficacy of controlled-release ropinirole (CR) (1-24 mg) administered once daily for 12 weeks in subjects with fibromyalgia Study Listed on ClinicalStudyDataRequest.com
ROP105323 Completed A Randomised, Double-Blind, Double-Dummy, Parallel Group Comparison of 24 Weeks of Treatment with Ropinirole Immediate Release Tablets (REQUIP IR) or Ropinirole Prolonged Release Tablets (SK&F-101468) in Advanced Stage Parkinson’s Disease Subjects who are not Adequately Controlled on L-dopa.
ROP106064 Completed Clinical Evaluation of Ropinirole PR/XR Tablets in Monotherapy for Parkinson's Disease - an Open-Label, Uncontrolled Study -
ROP109087 Completed An open label, repeat dose, dose escalation study conducted in Parkinson's Disease patients to characterize the pharmacokinetics and effect of food on ropinirole prolonged release (PR/CR) 12mg tablets. Study Listed on ClinicalStudyDataRequest.com

 

 

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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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