UnknownPhase 4

The Sedative Effects of Dexmedetomidine VS Propofol During Peribulbar Anesthesia in Patients Undergoing Vitrectomy Surgery

Egypt420 participantsStarted 2024-05-01

Plain-language summary

The aim of the work to compare the Sedative Effects of Dexmedetomidine and Propofol during peribulbar anesthesia in patients undergoing vitrectomy surgery on hemodynamic, respiratory parameters, recovery profile, analgesic effects, post-operative cognitive function, patients satisfaction and adverse events.

Who can participate

Age range20 Years – 70 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Age between 20-70 years. * Expected time of surgery less than 2 hours Exclusion Criteria: * patients with an initial mini mental state examination (MMSE) score less than 23 * Patients refusing LA * Clotting abnormalities * Impaired mental status * Allergy to any of the study medications * Also, patients were excluded if they had severe cardiac disease, chronic obstructive lung disease, a history of sleep apnea and those who received general anesthesia.

What they're measuring

Patient satisfaction

Timeframe: 6 hours after the end of surgery.

Trial details

NCT IDNCT06369103

SponsorBeni-Suef University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-05-01

Contact for this trial

Dina M Fakhry, MD

+201289998680 dina_fakhry_91@yahoo.com

View on ClinicalTrials.gov More Patient trials