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5 Resultados de la búsqueda.

ABPM Substudy GSK study Chronic Coronary Heart Disease NCT00799903

- 12/12/17 - 1 formulario, 4 itemgroups, 25 items, 1 idioma

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.

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

- 14/1/19 - 1 formulario, 4 itemgroups, 21 items, 1 idioma

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

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

- 20/9/21 - 1 formulario, 5 itemgroups, 18 items, 1 idioma

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

Blood pressure Pediatric surgery UKM - Blood pressure monitoring

- 4/12/16 - 1 formulario, 1 itemgroup, 6 items, 2 idiomas

Itemgroup: Blood pressure monitoring

Blood pressure monitoring form converted to ODM format. Routine documentation of University Hospital of Münster. Publication granted by Dr. med. V. Müller

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

- 13/8/17 - 1 formulario, 2 itemgroups, 19 items, 1 idioma

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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