Clinical Trials Directory

Trials / Completed

CompletedNCT07128719

Study Effects of Preoperative Modafinil on Recovery Profile of Morbidly Obese Patients Scheduled for Bariatric Surgery if it Can Enhance Recovery From Anesthesia

Study Effects of Preoperative Modafinil on Recovery Profile of Morbidly Obese Patients Scheduled for Bariatric Surgery

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Ain Shams University · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Accepted

Summary

study Effects of Preoperative Modafinil on Recovery Profile of Morbidly Obese Patients Scheduled for Bariatric Surgery if it Can Enhance Recovery From Anesthesia and provide improvement in recovery

Detailed description

The study was conducted to 20 patients scheduled for bariatric surgeries. The study group (Modafinil group) received oral 200 mg modafinil 8 hours before surgery and then another 200 mg 2 hours before surgery. The other group (Placebo group) were given placebo through the same regimen as Modafinil. Immediate recovery time, cognitive recovery, emotional (general) status, discharge from PACU according to modified Aldrete score were assessed.

Conditions

Interventions

TypeNameDescription
DRUGModafinildose of modafinil preoperatively for for active comparator

Timeline

Start date
2024-01-01
Primary completion
2025-01-01
Completion
2025-06-01
First posted
2025-08-19
Last updated
2025-08-19

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT07128719. Inclusion in this directory is not an endorsement.