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NCT04438915

The Effect of Obesity on the Incidence of Postoperative Cognitive Dysfunction in Gynecological Day Case Surgery

Completed NA Last updated 20 July 2021
What this trial tests

NA trial testing Effect of Obesity on incidence of Postoperative cognitive in Gynecological Day- Day- case surgery in Postoperative Cognitive Dysfunction in 138 participants. Completed in 20 May 2021.

Timeline
1 December 2020
Primary endpoint
20 May 2021
20 May 2021

Quick facts

Lead sponsorBeni-Suef University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposediagnostic
Enrollment138
Start date1 December 2020
Primary completion20 May 2021
Estimated completion20 May 2021
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Beni-Suef University

Who can join

Adults 20 to 40, female only, with Postoperative Cognitive Dysfunction. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Cognitive dysfunction is the impairment of mental process of perception. memory and information processing which allow the human to acquire knowledge and plan for the future. The etiology of Post operative cognitive dysfunction (POCD) is unclear and seems to be multifactorial involving a combination of patient, surgical, anesthetic and environmental factors. The definition of day surgery in Great Britain and Ireland is clear; the patient is admitted and discharged on the same day.

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 Postoperative Cognitive Dysfunction

Currently open trials in the same condition.

Other Beni-Suef University trials

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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/NCT04438915.

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