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Efficacy and Safety of Ropinirole XR (Extended Release) in Patients with Restless Legs Syndrome NCT00197080 - Ambulatory Blood Pressuure Monitoring Diary; Equipment Request

- 20/09/21 - 1 modulo, 5 itemgroups, 18 elementi, 1 linguaggio
Itemgroups: When dispensed?, Administrative, Ambulatory Blood Pressure Monitoring Diary, Blood Pressure Measurement, Equipment Request
Study ID: 101468/205 Clinical Study ID: 101468/205 Study Title:A 12-Week, Double-Blind, Placebo Controlled, Parallel Group Study to Assess the Efficacy and Safety of Ropinirole XR (Extended Release) in Patients with Restless Legs Syndrome Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00197080 Sponsor: GlaxoSmithKline Phase: phase 3 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Modutab,ZIPEREVE,ZEPREVE,REPREVE,ADARTREL,REQUIP,Zygara; Zygara,ZIPEREVE,ZEPREVE,Requip Depot,REQUIP,REPREVE,Modutab,ADARTREL Study Indication: Restless Legs Syndrome

Safety, tolerability and pharmacokinetics of repeat inhaled doses of milveterol in healthy subjects (Study ID: 101682) - 24hrs Ambulatory Blood Pressure Monitoring

- 14/01/19 - 1 modulo, 4 itemgroups, 21 elementi, 1 linguaggio
Itemgroups: Administrative data, Time documentation, 24hrs Ambulatory Blood pressure monitoring, Abnormalities
tudy ID: 101682 Clinical Study ID: B2E101682 Study Title: A randomised, double-blind, placebo-controlled, parallel group study to examine the safety, tolerability, and pharmacokinetics of repeat inhaled doses of GSK159797 in healthy subjects. Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: milveterol Trade Name: milveterol Study Indication: Pulmonary Disease, Chronic Obstructive

ABPM Substudy GSK study Chronic Coronary Heart Disease NCT00799903

- 12/12/17 - 1 modulo, 4 itemgroups, 25 elementi, 1 linguaggio
Itemgroups: ABPM Substudy Participation, Medical condition ABPM substudy, ABPM substudy, ABPM substudy Repeat assessments
Study ID: 100601 Clinical Study ID: LPL100601 Study Title: LPL100601, A Clinical Outcomes Study of Darapladib versus Placebo in Subjects with Chronic Coronary Heart Disease to Compare the Incidence of Major Adverse Cardiovascular Events (MACE) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00799903 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: darapladib Trade Name: darapladib Study Indication: Atherosclerosis Study part: ABPM Substudy.

Ambulatory Blood Pressure Monitoring Diary Restless Legs Syndrom NCT00355641 - Ambulatory Blood Pressure Monitoring Diary

- 13/08/17 - 1 modulo, 2 itemgroups, 19 elementi, 1 linguaggio
Itemgroups: General Information, Ambulatory Blood Pressure Monitoring
Study part: Ambulatory Blood Pressure Monitoring Diary. A 52-Week, Open-Label Study to Assess the Long-Term Safety of Ropinirole Extended Release (XR) in Patients with Restless Legs Syndrome (RLS). Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Clinicaltrials.gov Identifier: NCT00355641. Phase: phase 3. Study Recruitment Status: Completed. Generic Name: ropinirole. Trade Name Modutab, ZIPEREVE, ZEPREVE, REPREVE, ADARTREL, REQUIP, Zygara; Zygara, ZIPEREVE, ZEPREVE, Requip Depot, REQUIP, REPREVE, Modutab, ADARTREL. Study Indication : Restless Legs Syndrome. Study ID: 101468/206. Clinical Study ID: 101468/206.

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