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NCT02598050

Preoperative Cognitive Screening in Older Surgical Patients Utility for Predicting Morbidity

Completed Last updated 15 April 2021
What this trial tests

trial testing No Interventions as this is a observational study in Cognitive Impairment in 250 participants. Completed in 31 December 2017.

Timeline
1 February 2016
Primary endpoint
30 March 2017
31 December 2017

Quick facts

Lead sponsorBrigham and Women's Hospital
StatusCompleted
Study typeOBSERVATIONAL
Enrollment250
Start date1 February 2016
Primary completion30 March 2017
Estimated completion31 December 2017
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Brigham and Women's Hospital

Who can join

65 and older, any sex, with Cognitive Impairment. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this work is to determine whether preoperative cognitive screening of patients over the age of 65 can be used as predictor of postoperative outcomes in patients undergoing lower extremity surgical procedures. This work is important as it may aid patients, families and physicians about the appropriateness of the surgical procedure and in providing resources to patients who are at the highest risk of adverse outcomes.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Cognitive Impairment

Currently open trials in the same condition.

Other Brigham and Women's Hospital trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02598050.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing