Risultati di ricerca - Portale di modelli di dati medici (MDM-Portal)

7% CO2, GW597599, paroxetine andor alprazolam in healthy volunteers 100690 - Session 2 Day 2 Unscheduled

- 23/10/17 - 1 modulo, 3 itemgroups, 7 elementi, 1 linguaggio

Itemgroups: Administrative Documentation, Clinical Chemistry and Haematology, Urinalysis

Study ID: 100690 Clinical Study ID: NKP100690 Study Title: A randomised, double blind triple dummy, placebo controlled balanced incomplete block crossover study to evaluate the change in response to a 7% CO2 challenge and pharmacokinetics of single oral doses of GW597599 and paroxetine (5 or 7.5 mg) either alone or in combination, or alprazolam (0.75 mg) in healthy volunteers Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 1 Study Recruitment Status: Completed Generic Name: paroxetine Trade Name: Tagonis,Seroxat,Paxil,Paroxat,Deroxat,Aropax Study Indication: Depressive Disorder and Anxiety Disorders CRF Seiten: 255-365

7% CO2, GW597599, paroxetine andor alprazolam in healthy volunteers 100690 - Session 2Day 2

- 23/10/17 - 1 modulo, 3 itemgroups, 7 elementi, 1 linguaggio

Itemgroups: Administrative Documentation, Clinical Chemistry and Haematology, Urinalysis

Study ID: 100690 Clinical Study ID: NKP100690 Study Title: A randomised, double blind triple dummy, placebo controlled balanced incomplete block crossover study to evaluate the change in response to a 7% CO2 challenge and pharmacokinetics of single oral doses of GW597599 and paroxetine (5 or 7.5 mg) either alone or in combination, or alprazolam (0.75 mg) in healthy volunteers Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 1 Study Recruitment Status: Completed Generic Name: paroxetine Trade Name: Tagonis,Seroxat,Paxil,Paroxat,Deroxat,Aropax Study Indication: Depressive Disorder and Anxiety Disorders CRF Seiten: 255-365

L-dopa controlled study of ropinirole, neuroprotective effect and ophthalmological safety in early Parkinson’s disease 101468/125 Module 1 Visit 3 Week 2 (optional visit)

- 12/10/17 - 1 modulo, 5 itemgroups, 8 elementi, 1 linguaggio

Itemgroups: Vital signs, Concomitant medication, Adverse Experiences, Study Medication Compliance, Patient continuation

Study ID: 101468/125 Clinical Study ID: SKF-101468/125 Study Title: A double-blind, multicentre, flexible dose, L-dopa controlled study of ropinirole to investigate A) neuroprotective effect as measured by 3D PET scanning, and B) ophthalmological safety, in patients with early Parkinson’s disease Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: requip Study Indication: Restless Legs Syndrome

L-dopa controlled study of ropinirole, neuroprotective effect and ophthalmological safety in early Parkinson’s disease 101468/125 Module 1 Screening/Baseline Conclusion

- 12/10/17 - 1 modulo, 2 itemgroups, 5 elementi, 1 linguaggio

Itemgroups: Screening Baseline Conclusion, Investigator´s signature

Study ID: 101468/125 Clinical Study ID: SKF-101468/125 Study Title: A double-blind, multicentre, flexible dose, L-dopa controlled study of ropinirole to investigate A) neuroprotective effect as measured by 3D PET scanning, and B) ophthalmological safety, in patients with early Parkinson’s disease Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: requip Study Indication: Restless Legs Syndrome

GSK Ropinirole in Subjects with Restless Legs Syndrome 101468/191 Screening (Form 1)

- 30/08/17 - 1 modulo, 19 itemgroups, 84 elementi, 1 linguaggio

Itemgroups: General Information, RLS Screen History, RLS Diagnostic Criteria, Demography, Vital signs, Orthostatic Vital Signs, Electrocardiogramm (12 Lead), Physical Examination, Laboratory Evaluation, Pregnancy Dipstick, Significant medical/surgical history and physical examination, List of diagnosis other than RLS or PLMS, Prior and Concomitant Medication, Details prior and concomitant medication, RLS Pharmacotherapy history, Details RLS pharmacotherapy history, Screening Inclusion Criteria, Screening Exclusion Criteria, Repeat Electrocardiogram

Study ID: 101468/191 Clinical Study ID: SKF-101468/191 Study Title:A 12 Week, Double-Blind, Placebo-Controlled, Parallel Group Study to Assess the Efficacy, Safety and Tolerability of Ropinirole in Subjects with Restless Legs Syndrome (RLS) Suffering from Periodic Leg Movements of Sleep (PLMS) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Requip Study Indication: Restless Legs Syndrome