Ketofol Versus Dexmedetomidine for Prevention of Emergence Delirium in Pediatric Patients Undergoing Squint Surgeries: A Randomized Controlled Study.

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1/Phase 2
SUMMARY

The aim of the study is to compare the effectiveness of ketofol for the prevention of emergence delirium in pediatric patients undergoing squint surgery, in comparison to dexmedetomidine.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 2
Maximum Age: 6
Healthy Volunteers: t
View:

• • All pediatric patients aged 2 to 6 years.

‣ Both sexes.

⁃ ASA physical status I and II.

⁃ Patients undergoing squint surgery.

Locations
Other Locations
Egypt
Abu ElResh hospital
NOT_YET_RECRUITING
Cairo
Abu Elresh Hospitals ( Cairo university )
RECRUITING
Cairo
Contact Information
Primary
Muhammad Kh Ibrahim
dr.mki26413@gmail.com
+201032170260
Backup
Mohamed El Abdelfatah
mohyaseen2@gmail.com
+201272288695
Time Frame
Start Date: 2024-08-10
Estimated Completion Date: 2024-11-10
Participants
Target number of participants: 46
Treatments
Experimental: Ketofol Group
Five minutes after induction; Ketofol (ketamine to propofol ratio 1:4) will be infused at a rate of 0.6 ml/kg/hr. Ketofol will be prepared by adding 40 mg of ketamine to 160 mg of propofol and diluted to 20 ml with normal saline 0.9%.
Experimental: Dexmedetomidine
Five minutes after securing the airway, dexmedetomidine infusion will be started at a rate of 0.2 mcg/kg/hr.
Related Therapeutic Areas
Sponsors
Leads: Cairo University

This content was sourced from clinicaltrials.gov

Similar Clinical Trials