Trial · NCT01631825
Results by group127
Each measurement the trial posted, group by group, in the words and numbers it posted.
1 to 20 of 127
Download this page as JSON| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Incidence and Severity of Adverse Events (AEs), Vital Signs, and Laboratory Parameters | SPM 962 | Any AEs | 311 | participants | |
| Incidence and Severity of Adverse Events (AEs), Vital Signs, and Laboratory Parameters | SPM 962 | Treatment-related AEs | 269 | participants | |
| Incidence and Severity of Adverse Events (AEs), Vital Signs, and Laboratory Parameters | SPM 962 | SAEs | 34 | participants | |
| Incidence and Severity of Adverse Events (AEs), Vital Signs, and Laboratory Parameters | SPM 962 | Treatment-related SAEs | 6 | participants | |
| Incidence and Severity of Adverse Events (AEs), Vital Signs, and Laboratory Parameters | SPM 962 | Severe AEs | 16 | participants | |
| Incidence and Severity of Adverse Events (AEs), Vital Signs, and Laboratory Parameters | SPM 962 | Discontinuation due to AEs | 47 | participants | |
| Incidence and Severity of Adverse Events (AEs), Vital Signs, and Laboratory Parameters | SPM 962 | Death | 1 | participants | |
| Incidence and Severity of Adverse Events (AEs), Vital Signs, and Laboratory Parameters | SPM 962 | AEs of special interest 1 | 7 | participants | |
| Incidence and Severity of Adverse Events (AEs), Vital Signs, and Laboratory Parameters | SPM 962 | AEs of special interest 2 | 4 | participants | |
| Incidence and Severity of Adverse Events (AEs), Vital Signs, and Laboratory Parameters | SPM 962 | AEs of special interest 3 | 54 | participants | |
| Incidence and Severity of Adverse Events (AEs), Vital Signs, and Laboratory Parameters | SPM 962 | Valvular disease of the heart | 0 | participants | |
| Incidence and Severity of Adverse Events (AEs), Vital Signs, and Laboratory Parameters | SPM 962 | Sitting systolic blood pressure, ≤ 100 mmHg | 9 | participants | |
| Incidence and Severity of Adverse Events (AEs), Vital Signs, and Laboratory Parameters | SPM 962 | QTcB ≥ 500 ms | 5 | participants | |
| Incidence and Severity of Adverse Events (AEs), Vital Signs, and Laboratory Parameters | SPM 962 | QTcF ≥ 500 ms | 2 | participants | |
| Incidence and Severity of Adverse Events (AEs), Vital Signs, and Laboratory Parameters | SPM 962 | Application site reaction ≥ +++ | 14 | participants | |
| Incidence and Severity of Adverse Events (AEs), Vital Signs, and Laboratory Parameters | SPM 962 | Weight decrease reported as AE | 8 | participants | |
| Unified Parkinson's Disease Rating Scale (UPDRS) Part 3 Sum Score | SPM 962 | Week 12 | -8.3 | Standard Deviation 7.1 | Scores on a scale |
| Unified Parkinson's Disease Rating Scale (UPDRS) Part 3 Sum Score | SPM 962 | Week 24 | -8.0 | Standard Deviation 7.6 | Scores on a scale |
| Unified Parkinson's Disease Rating Scale (UPDRS) Part 3 Sum Score | SPM 962 | Week 52 | -7.5 | Standard Deviation 8.6 | Scores on a scale |
| UPDRS Part 2 Sum Score (Average of on State and Off State) | SPM 962 | Week 12 | -2.6 | Standard Deviation 3.0 | Scores on a scale |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
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GET https://conductscience.org/api/trials/v1/NCT01631825/results