Trial · NCT02009163
Results by group108
Each measurement the trial posted, group by group, in the words and numbers it posted.
1 to 20 of 108
Download this page as JSON| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Time to Relapse From Date of Randomization to Endpoint of The Randomized-withdrawal Period | Placebo (Randomized-withdrawal Period) | NA | Inter-Quartile Range 55.0 to NA | days | |
| Time to Relapse From Date of Randomization to Endpoint of The Randomized-withdrawal Period | SPD489 (Randomized-withdrawal Period) | NA | Inter-Quartile Range NA to NA | days | |
| Change From Randomized-Withdrawal Baseline in The Number of Binge- Eating Days Per Week During The Randomized-withdrawal Period | Placebo (Randomized-withdrawal Period) | 0.63 | Standard Error 0.076 | days | |
| Change From Randomized-Withdrawal Baseline in The Number of Binge- Eating Days Per Week During The Randomized-withdrawal Period | SPD489 (Randomized--Withdrawal Period) | 0.02 | Standard Error 0.061 | days | |
| Percent of Participants Within Each Category of The Clinical Global Impression-Severity of Illness (CGI-S) Scale at Endpoint of The Randomized-withdrawal Period | Placebo (Randomized-withdrawal Period) | Normal, Not at All Ill | 45.0 | percentage of participants | |
| Percent of Participants Within Each Category of The Clinical Global Impression-Severity of Illness (CGI-S) Scale at Endpoint of The Randomized-withdrawal Period | SPD489 (Randomized-withdrawal Period) | Normal, Not at All Ill | 81.6 | percentage of participants | |
| Percent of Participants Within Each Category of The Clinical Global Impression-Severity of Illness (CGI-S) Scale at Endpoint of The Randomized-withdrawal Period | Placebo (Randomized-withdrawal Period) | Borderline Mentally Ill | 10.7 | percentage of participants | |
| Percent of Participants Within Each Category of The Clinical Global Impression-Severity of Illness (CGI-S) Scale at Endpoint of The Randomized-withdrawal Period | SPD489 (Randomized-withdrawal Period) | Borderline Mentally Ill | 11.8 | percentage of participants | |
| Percent of Participants Within Each Category of The Clinical Global Impression-Severity of Illness (CGI-S) Scale at Endpoint of The Randomized-withdrawal Period | Placebo (Randomized-withdrawal Period) | Mildly Ill | 14.5 | percentage of participants | |
| Percent of Participants Within Each Category of The Clinical Global Impression-Severity of Illness (CGI-S) Scale at Endpoint of The Randomized-withdrawal Period | SPD489 (Randomized-withdrawal Period) | Mildly Ill | 2.2 | percentage of participants | |
| Percent of Participants Within Each Category of The Clinical Global Impression-Severity of Illness (CGI-S) Scale at Endpoint of The Randomized-withdrawal Period | Placebo (Randomized-withdrawal Period) | Moderately Ill | 22.1 | percentage of participants | |
| Percent of Participants Within Each Category of The Clinical Global Impression-Severity of Illness (CGI-S) Scale at Endpoint of The Randomized-withdrawal Period | SPD489 (Randomized-withdrawal Period) | Moderately Ill | 2.2 | percentage of participants | |
| Percent of Participants Within Each Category of The Clinical Global Impression-Severity of Illness (CGI-S) Scale at Endpoint of The Randomized-withdrawal Period | Placebo (Randomized-withdrawal Period) | Markedly Ill | 6.9 | percentage of participants | |
| Percent of Participants Within Each Category of The Clinical Global Impression-Severity of Illness (CGI-S) Scale at Endpoint of The Randomized-withdrawal Period | SPD489 (Randomized-withdrawal Period) | Markedly Ill | 2.2 | percentage of participants | |
| Percent of Participants Within Each Category of The Clinical Global Impression-Severity of Illness (CGI-S) Scale at Endpoint of The Randomized-withdrawal Period | Placebo (Randomized-withdrawal Period) | Severely Ill | 0.0 | percentage of participants | |
| Percent of Participants Within Each Category of The Clinical Global Impression-Severity of Illness (CGI-S) Scale at Endpoint of The Randomized-withdrawal Period | SPD489 (Randomized-withdrawal Period) | Severely Ill | 0.0 | percentage of participants | |
| Percent of Participants Within Each Category of The Clinical Global Impression-Severity of Illness (CGI-S) Scale at Endpoint of The Randomized-withdrawal Period | Placebo (Randomized-withdrawal Period) | Among the Most Extremely Ill | 0.8 | percentage of participants | |
| Percent of Participants Within Each Category of The Clinical Global Impression-Severity of Illness (CGI-S) Scale at Endpoint of The Randomized-withdrawal Period | SPD489 (Randomized-withdrawal Period) | Among the Most Extremely Ill | 0.0 | percentage of participants | |
| Change From Randomized-Withdrawal Baseline in The Total Score of The Yale-Brown Obsessive Compulsive Scale Modified for Binge Eating (Y-BOCS-BE) During The Randomized-withdrawal Period | Placebo (Randomized-withdrawal Period) | 5.5 | Standard Error 0.66 | units on a scale | |
| Change From Randomized-Withdrawal Baseline in The Total Score of The Yale-Brown Obsessive Compulsive Scale Modified for Binge Eating (Y-BOCS-BE) During The Randomized-withdrawal Period | SPD489 (Randomized-withdrawal Period) | -0.0 | Standard Error 0.52 | units 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/NCT02009163/results