Trial · NCT02507505
Outcomes12
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
1 to 12 of 12
Download this page as JSON| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Death or Inability to Walk 10 Feet or Across a Room Without Human Assistance | Approximately 60 days after Randomization | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Overall Health and Disability | Approximately 60, 180, and 365 days after randomization | Patients providing data at each time point | score on a scale | MEDIAN |
| SECONDARY | Ability to Return to Home | Approximately 60, 180, and 365 days after randomization | This outcome was assessed among patients who were not admitted from a nursing home, rehabilitation facility, or acute care hospital. Denominator includes all known decedents at each time point, plus survivors providing information on location of residence at the time of study interview. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Chronic Pain | Approximately 60, 180, and 365 days after randomization | Numbers differ across rows due to missing data | units on a scale | MEAN |
| SECONDARY | Cognitive Function | Baseline and approximately 60, 180, and 365 days after randomization | Numbers differ across rows due to missing data | units on a scale | MEDIAN |
| SECONDARY | All-cause Mortality | Approximately 60, 180, and 365 days after randomization | All enrolled patients who had not withdrawn or been lost to follow up a given study time point | participants | NUMBER |
| SECONDARY | Need for Assistive Devices for Walking | Approximately 60, 180, and 365 days after randomization | 60-day outcome | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Acute Postoperative Pain | Before surgery and daily through postoperative day 3 or day of discharge, whichever occurs first | units on a scale | MEAN | |
| SECONDARY | Satisfaction With Care | Postoperative day 3 or day of discharge, whichever occurs first | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Postoperative Delirium | Baseline and daily through postoperative day 3 or day of discharge, whichever occurs first | This outcome was assessed only among patients who had a negative 3D-CAM assessment for delirium before randomization. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Inpatient Mortality | During initial hospitalization until day of discharge or 30 days after randomization, whichever occurs first | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Major Inpatient Morbidity | During initial hospitalization until day of discharge or 30 days after randomization, whichever occurs first | Participants | COUNT_OF_PARTICIPANTS |
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
Read this list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT02507505/outcomes