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| Study Type: | Interventional |
|---|---|
| Study Design: | Non-Randomized, Open Label, Single Group Assignment |
| Condition: |
Parkinson's Disease |
| Intervention: |
Drug: Rotigotine |
Participant Flow
| Key information relevant to the recruitment process for the overall study, such as dates of the recruitment period and locations |
|---|
| 124 patients were screened. 5 patients were run-in failures and 3 patients were screen failures. 116 patients started treatment, i.e. were included into the Safety Set. 114 patients were included into the Full Analysis Set. 99 patients completed the treatment period. 2 patients withdrew after the treatment period. 97 patients completed the study. |
| Significant events and approaches for the overall study following participant enrollment, but prior to group assignment |
|---|
| No text entered. |
| Description | |
|---|---|
| Rotigotine | Patients were dispensed rotigotine patches up to 8mg/24h at a dose considered by the investigator to be equivalent to the dose of ropinirole that the subject was currently taking. |
| Rotigotine | |
|---|---|
| STARTED | 124 |
| Start of Treatment - Safety Set | 116 |
| Full Analysis Set | 114 |
| Treatment Period Completed | 99 |
| COMPLETED | 97 |
| NOT COMPLETED | 27 |
| Adverse Event | 13 |
| Withdrawal by Subject | 1 |
| Protocol Violation | 3 |
| Lost to Follow-up | 2 |
| Run-In Failure | 5 |
| Screen Failure | 3 |
Baseline Characteristics
| Description | |
|---|---|
| Rotigotine | Patients were dispensed rotigotine patches up to 8mg/24h at a dose considered by the investigator to be equivalent to the dose of ropinirole that the subject was currently taking. |
| Rotigotine | |
|---|---|
|
Number of Participants [units: participants] |
116 |
|
Age [units: participants] |
|
| <=18 years | 0 |
| Between 18 and 65 years | 73 |
| >=65 years | 43 |
|
Age [units: years] Mean ± Standard Deviation |
60.0 ± 10.1 |
|
Gender [units: participants] |
|
| Female | 69 |
| Male | 47 |
|
Region of Enrollment [units: participants] |
|
| Korea, Republic of | 116 |
Outcome Measures
| 1. Primary: | Change in Pulse Rate (Supine, After 1 Minute) |
| 2. Primary: | Change in Systolic Blood Pressure (Supine, After 1 Minute) |
| 3. Primary: | Change in Diastolic Blood Pressure (Supine, After 1 Minute) |
| 4. Primary: | Change in Pulse Rate (Supine, After 5 Minutes) |
| 5. Primary: | Change in Systolic Blood Pressure (Supine, After 5 Minutes) |
| 6. Primary: | Change in Diastolic Blood Pressure (Supine, After 5 Minutes) |
| 7. Primary: | Change in Pulse Rate (Standing, After 1 Minute) |
| 8. Primary: | Change in Systolic Blood Pressure (Standing, After 1 Minute) |
| 9. Primary: | Change in Diastolic Blood Pressure (Standing, After 1 Minute) |
| 10. Primary: | Change in Pulse Rate (Standing, After 3 Minutes) |
| 11. Primary: | Change in Systolic Blood Pressure (Standing, After 3 Minutes) |
| 12. Primary: | Change in Diastolic Blood Pressure (Standing, After 3 Minutes) |
| 13. Primary: | Change in Heart Rate |
| 14. Primary: | Change in PR Interval |
| 15. Primary: | Change in QRS Duration |
| 16. Primary: | Change in QT Interval |
| 17. Primary: | Change in QT Interval Corrected for Heart Rate According to Bazett's Formula (QTcB) |
| 18. Primary: | Change in Percentage of Basophilic Granulocytes in White Blood Cell Count |
| 19. Primary: | Change in Percentage of Eosinophilic Granulocytes in White Blood Cell Count |
| 20. Primary: | Change in Hematocrit |
| 21. Primary: | Change in Hemoglobin |
| 22. Primary: | Change in Percentage of Lymphocytes in White Blood Cell Count |
| 23. Primary: | Change in Percentage of Monocytes in White Blood Cell Count |
| 24. Primary: | Change in Percentage of Neutrophilic Granulocytes Segmented in White Blood Cell Count |
| 25. Primary: | Change in Platelet Count |
| 26. Primary: | Change in Red Blood Cell Count |
| 27. Primary: | Change in White Blood Cell Count |
| 28. Primary: | Change in Albumin |
| 29. Primary: | Change in Alkaline Phosphatase |
| 30. Primary: | Change in Blood Urea Nitrogen |
| 31. Primary: | Change in Calcium |
| 32. Primary: | Change in Chloride |
| 33. Primary: | Change in Creatinine |
| 34. Primary: | Change in Gamma-Glutamyltransferase |
| 35. Primary: | Change in Glucose |
| 36. Primary: | Change in Inorganic Phosphate |
| 37. Primary: | Change in Potassium |
| 38. Primary: | Change in Serum Glutamic Oxaloacetic Transaminase |
| 39. Primary: | Change in Glutamic Pyruvic Transaminase |
| 40. Primary: | Change in Sodium |
| 41. Primary: | Change in Total Bilirubin |
| 42. Primary: | Change in Total Protein |
| 43. Primary: | Change in Uric Acid |
| 44. Primary: | Occurrence of Abnormal, Clinically Relevant Events in Physical Examination for ‘Ears, Eyes, Nose, Mouth, Throat’ |
| 45. Primary: | Occurrence of Abnormal, Clinically Relevant Events in Physical Examination for ‘Psychiatric’ |
| 46. Primary: | Occurrence of Abnormal, Clinically Relevant Events in Physical Examination for ‘Hematological/Lymphatic Nodes’ |
| 47. Primary: | Occurrence of Abnormal, Clinically Relevant Events in Physical Examination for ‘Dermatological’ |
| 48. Primary: | Occurrence of Abnormal, Clinically Relevant Events in Physical Examination for ‘Cardiovascular’ |
| 49. Primary: | Occurrence of Abnormal, Clinically Relevant Events in Physical Examination for ‘Peripheral Vascular’ |
| 50. Primary: | Occurrence of Abnormal, Clinically Relevant Events in Physical Examination for ‘Pulmonary’ |
| 51. Primary: | Occurrence of Abnormal, Clinically Relevant Events in Physical Examination for ‘Musculoskeletal’ |
| 52. Primary: | Occurrence of Abnormal, Clinically Relevant Events in Physical Examination for ‘Hepato-/Gastrointestinal’ |
| 53. Primary: | Occurrence of Abnormal, Clinically Relevant Events in Physical Examination for ‘Renal/Genitourological’ |
| 54. Primary: | Occurrence of Abnormal, Clinically Relevant Events in Physical Examination for ‘Metabolic/Endocrine’ |
| 55. Primary: | Occurrence of Abnormal, Clinically Relevant Events in Physical Examination for ‘Other’ |
| 56. Primary: | Occurrence of Abnormal, Clinically Relevant Events in Neurological Examination for ‘Mental Status’ |
| 57. Primary: | Occurrence of Abnormal, Clinically Relevant Events in Neurological Examination for ‘Deep Tendon Reflexes’ |
| 58. Primary: | Occurrence of Abnormal, Clinically Relevant Events in Neurological Examination for ‘Muscle Strength’ |
| 59. Primary: | Occurrence of Abnormal, Clinically Relevant Events in Neurological Examination for ‘Cranial Nerve Function’ |
| 60. Primary: | Occurrence of Abnormal, Clinically Relevant Events in Neurological Examination for ‘Plantar Reflex’ |
| 61. Primary: | Occurrence of Abnormal, Clinically Relevant Events in Neurological Examination for ‘Gait’ |
| 62. Primary: | Occurrence of Abnormal, Clinically Relevant Events in Neurological Examination for ‘Coordination/Balance’ |
| 63. Primary: | Occurrence of Abnormal, Clinically Relevant Events in Neurological Examination for ‘Involuntary Movements’ |
| 64. Primary: | Occurrence of Abnormal, Clinically Relevant Events in Neurological Examination for ‘Sensory Perception’ |
| 65. Primary: | Occurrence of Abnormal, Clinically Relevant Events in Neurological Examination for ‘Other’ |
| 66. Primary: | Completion of Trial From Baseline to End of Treatment |
| 67. Primary: | Completion of Trial on the Original Treatment Assignment From Baseline to End of Treatment |
| 68. Primary: | Drop-out During the 5 Half-life Overlap Period Due to Adverse Events (AEs) |
| 69. Primary: | Drop-out Due to Adverse Events (AEs) With Onset During the 5 Half-life Overlap Period |
| 70. Primary: | Dose Reduction During the 5 Half-life Overlap Period Due to Adverse Events (AEs) |
| 71. Primary: | Dose Reduction Due to Adverse Events (AEs) With Onset During the 5 Half-life Overlap Period |
| 72. Secondary: | Change in Unified Parkinson's Disease Rating Scale (UPDRS) Part I Score From Baseline to End of Treatment |
| 73. Secondary: | Change in Unified Parkinson's Disease Rating Scale (UPDRS) Part II Score From Baseline to End of Treatment |
| 74. Secondary: | Change in Unified Parkinson's Disease Rating Scale (UPDRS) Part III Score From Baseline to End of Treatment |
| 75. Secondary: | Change in Unified Parkinson's Disease Rating Scale (UPDRS) Part IV Score From Baseline to End of Treatment |
| 76. Secondary: | Change in Parkinson’s Disease Sleep Scale (PDSS) Sum Score From Baseline to End of Treatment |
| 77. Secondary: | Change in Epworth Sleepiness Scale (ESS) Sum Score From Baseline to End of Treatment |
| 78. Secondary: | Change in Parkinson’s Disease Non-Motor Symptom Assessment Scale (PDNMS) Total Sum Score From Baseline to End of Treatment |
| 79. Secondary: | Change in Clinical Global Impression (CGI) Item 1 Score From Baseline to End of Treatment |
| 80. Secondary: | Clinical Global Impression (CGI) Item 2 Score |
| 81. Secondary: | Clinical Global Impression (CGI) Item 3.1 |
| 82. Secondary: | Clinical Global Impression (CGI) Item 3.2 |
| 83. Secondary: | Patient Global Impression (PGI) Item 1 Score |
| 84. Secondary: | Patient Global Impression (PGI) Item 2 |
| 85. Secondary: | Patient Global Impression (PGI) Item 3 |
| 86. Secondary: | Change in Short-form Parkinson's Disease Questionnaire (PDQ-8) Single Index Score From Baseline to End of Treatment |
| 87. Secondary: | Patient Treatment Preference Scale Question 1 |
| 88. Secondary: | Patient Treatment Preference Scale Question 2 |
| 89. Secondary: | Patient Treatment Preference Scale Question 3 |
| 90. Secondary: | Patient Treatment Preference Scale Question 4 |
| 91. Secondary: | Patient Treatment Preference Scale Question 5 |
| 92. Secondary: | Patient Treatment Preference Scale Question 6 |
| 93. Secondary: | Patient Treatment Preference Scale Question 7 |
More Information
| Principal Investigators are NOT employed by the organization sponsoring the study. | ||||||
| There IS an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed. | ||||||
The agreement is:
|
| Limitations of the study, such as early termination leading to small numbers of participants analyzed and technical problems with measurement leading to unreliable or uninterpretable data |
|---|
| No text entered. |
| Responsible Party: | UCB ( Study Director ) |
| Study ID Numbers: | SP908 |
| Study First Received: | December 21, 2007 |
| Results First Received: | December 17, 2008 |
| Last Updated: | November 5, 2009 |
| ClinicalTrials.gov Identifier: | NCT00593606 History of Changes |
| Health Authority: | Korea: Food and Drug Administration |