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Parkinsons Disease ×
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Table of contents
  1. 1. Clinical Trial
  2. 2. Routine Documentation
  3. 3. Registry/Cohort Study
  4. 4. Quality Assurance
  5. 5. Data Standard
  6. 6. Patient-Reported Outcome
  7. 7. Medical Specialty
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395 Search results.

Adverse Events & Concomitant Medications Week 3 (Visit 7) Ropinirole Parkinson Disease 101468/165 - Adverse Events & Concomitant Medications Week 3 (Visit 7)

- 10/30/19 - 1 form, 1 itemgroup, 5 items, 1 language
Itemgroup: Adverse Events; Concomitant Medications
Study Part: Adverse Events & Concomitant Medications Week 3 (Visit 7). An open-label, up-titration study to assess the dose proportionality of ropinirole controlled release (CR) and to demonstrate the bioequivalence of ropinirole CR (1 x 8 mg) compared to the ropinirole CR (4 x 2 mg) in Parkinson's Disease patients not receiving other dopaminergic therapies. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Phase: phase 2. Study Recruitment Status: Completed. Generic Name: ropinirole. Trade Name: Modutab, ZIPEREVE, ZEPREVE, REPREVE, ADARTREL, REQUIP,Zygara. Study Indication: Parkinson Disease. Study ID: 101468/165. Clinical Study ID: 101468/165

Eligibility Parkinson's Disease NCT01607697

- 1/17/19 - 1 form, 2 itemgroups, 10 items, 1 language
Itemgroups: Inclusion Criteria, Exclusion Criteria
Mindfulness Based Intervention (MBI) on the Quality of Life and Non-Motor Symptoms (NMS) of Persons With PD; ODM derived from: https://clinicaltrials.gov/show/NCT01607697

Eligibility Parkinson's Disease NCT01673724

- 1/17/19 - 1 form, 2 itemgroups, 10 items, 1 language
Itemgroups: Inclusion Criteria, Exclusion Criteria
Pramipexole and Bromocriptine on Nonmotor Symptoms of Early Parkinson's Disease; ODM derived from: https://clinicaltrials.gov/show/NCT01673724

Eligibility Parkinson's Disease NCT01590056

- 1/17/19 - 1 form, 2 itemgroups, 9 items, 1 language
Itemgroups: Inclusion Criteria, Exclusion Criteria
Emotional and Cognitive Subthalamic Nucleus in Deep Brain Stimulation Treated Parkinson Patients; ODM derived from: https://clinicaltrials.gov/show/NCT01590056

Eligibility Parkinson's Disease NCT01572142

- 1/17/19 - 1 form, 2 itemgroups, 10 items, 1 language
Itemgroups: Inclusion Criteria, Exclusion Criteria
Decrease in Sense of Smell and Associated Cognitive Decline in Parkinson's Disease; ODM derived from: https://clinicaltrials.gov/show/NCT01572142

Eligibility Parkinson`s Disease - Autonomic Dysregulation NCT01518751

- 1/17/19 - 1 form, 1 itemgroup, 11 items, 1 language
Itemgroup: Criteria
Orthostatic Dysregulation and Associated Gastrointestinal Dysfunction in Parkinson's Disease - Evolution; ODM derived from: https://clinicaltrials.gov/show/NCT01518751

Eligibility Idiopathic Parkinson's Disease NCT01028586

- 8/19/18 - 1 form, 2 itemgroups, 10 items, 1 language
Itemgroups: Inclusion Criteria, Exclusion Criteria
MOTION, Safinamide in Early Idiopathic Parkinson's Disease (IPD), as add-on to Dopamine Agonist (Extension of Trial 27918); ODM derived from: https://clinicaltrials.gov/show/NCT01028586

L-dopa controlled study of ropinirole, neuroprotective effect and ophthalmological safety in early Parkinson’s disease 101468/125 - Module 3 Visit 6 Month 6

- 12/20/17 - 1 form, 18 itemgroups, 51 items, 1 language
Itemgroups: Current Dose Level, Vital signs, Concomitant Medication, Adverse Experiences, L-Dopa Rescue, Study Medication Compliance, End of visit instructions for patients continuing, End of visit instructions for patients not continuing, ERG Examintion Appointment Card, Concomitant Medication, Details on concomitant medication, Levodopa Rescue Therapy, Details on Levodopa - rescue therapy, Adverse Experiences, Details on Adverse Experiences, Investigator´s Signature, Patient Continuation / Withdrawal, 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

status of treatment blind Ropinirole CR Ropinirole IR Monotherapy 101468/168

- 12/6/17 - 1 form, 2 itemgroups, 6 items, 1 language
Itemgroups: administrative data, Status of treatment blind
Study ID: 101468/168 Clinical Study ID: 101468/168 Study Title: A Randomised, Double Blind, Three Period, Cross-Over Study of Ropinirole CR and Ropinirole IR Monotherapy 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: Modutab,ZIPEREVE,ZEPREVE,REPREVE,ADARTREL,REQUIP,Zygara Study Indication: Parkinson Disease

Unified Parkinson's Disease Rating Scale (Fahn et al. 1987) (UPDRS) - Unified Parkinson's Disease Rating Scale (Fahn et al. 1987)(UPDRS)

- 11/14/17 - 1 form, 12 itemgroups, 107 items, 2 languages
Itemgroups: Mentation, behaviour and mood (UPDRS), ON Activities of daily living (UPDRS), OFF Activities of daily living (UPDRS), ON Motor Examination (UPDRS), OFF Motor Examination (UPDRS), ON Complications of therapy - dyskinesias (in the past week) (UPDRS), OFF Complications of therapy - dyskinesias (in the past week) (UPDRS), ON Complications of therapy - clinical fluctuations (in the past week) (UPDRS), OFF Complications of therapy - clinical fluctuations (in the past week) (UPDRS), ON Complications of therapy - other complications (in the past week) (UPDRS), OFF Complications of therapy - other complications (in the past week) (UPDRS), UPDRS Result
Unified Parkinson's Disease Rating Scale (Fahn et al. 1987).

Early withdrawal physical examination Ropinirole CR Ropinirole IR Monotherapy 101468/168

- 11/3/17 - 1 form, 10 itemgroups, 16 items, 1 language
Itemgroups: administrative data, vital signs, clinical global impression questionnaire, unified parkinson's disease rating scale questionnaire, parkinson's disease sleep scale, Beck Depression Inventory, Epworth Sleepiness Scale, pregnancy test, 12-lead ECG, central laboratory
Study ID: 101468/168 Clinical Study ID: 101468/168 Study Title: A Randomised, Double Blind, Three Period, Cross-Over Study of Ropinirole CR and Ropinirole IR Monotherapy 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: Modutab,ZIPEREVE,ZEPREVE,REPREVE,ADARTREL,REQUIP,Zygara Study Indication: Parkinson Disease

visit week 36 physical examination Ropinirole CR Ropinirole IR Monotherapy 101468/168

- 11/3/17 - 1 form, 9 itemgroups, 15 items, 1 language
Itemgroups: administrative data, vital signs, clinical global impression questionnaire, unified parkinson's disease rating scale questionnaire, parkinson's disease sleep scale, Beck Depression Inventory, Epworth Sleepiness Scale, 12-lead ECG, central laboratory
Study ID: 101468/168 Clinical Study ID: 101468/168 Study Title: A Randomised, Double Blind, Three Period, Cross-Over Study of Ropinirole CR and Ropinirole IR Monotherapy 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: Modutab,ZIPEREVE,ZEPREVE,REPREVE,ADARTREL,REQUIP,Zygara Study Indication: Parkinson Disease