Trial · NCT01551758
Trial comparisons12
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
1 to 12 of 12
Download this page as JSON| Comparison | Source |
|---|---|
| FF/VI 100 mcg/25 mcg vs Usual Care: Time to an Event of Discontinuation of Initial Therapy Occurring in a Year | Trial comparisons |
| FF/VI 100 mcg/25 mcg vs Usual Care: Time to the First Serious Adverse Event of Pneumonia Occuring in a Year | Trial comparisons |
| FF/VI 100 mcg/25 mcg vs Usual Care: Number of Participants With Non-serious Adverse Drug Reactions (ADR) | Trial comparisons |
| FF/VI 100 mcg/25 mcg vs Usual Care: Time to First Moderate/Severe Exacerbations on Initial Therapy Occurring in a Year | Trial comparisons |
| FF/VI 100 mcg/25 mcg vs Usual Care: Number of Participants With Serious Adverse Events (SAEs) of Pneumonia During the Study | Trial comparisons |
| FF/VI 100 mcg/25 mcg vs Usual Care: Time to First Moderate/Severe Exacerbations Occurring in a Year | Trial comparisons |
| FF/VI 100 mcg/25 mcg vs Usual Care: Time to the Addition of a Further COPD Controller Medication Occurring in a Year | Trial comparisons |
| FF/VI 100 mcg/25 mcg vs Usual Care: Time to First Severe Exacerbations Occurring in a Year | Trial comparisons |
| FF/VI 100 mcg/25 mcg vs Usual Care: Number of Participants With Serious Adverse Drug Reactions | Trial comparisons |
| FF/VI 100 mcg/25 mcg vs Usual Care: Number of Participants With Serious Adverse Events | Trial comparisons |
| FF/VI 100 mcg/25 mcg vs Usual Care: Number of Participants With Fatal Serious Adverse Events of Pneumonia | Trial comparisons |
| FF/VI 100 mcg/25 mcg vs Usual Care: serious adverse events | Trial comparisons |
trials-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
Read this list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT01551758/comparisons