144
Participants
Start Date
December 15, 2024
Primary Completion Date
June 15, 2025
Study Completion Date
July 16, 2025
Gabapentin Group (Group G): Patients will receive 300 mg of oral Gabapentin
In this study, the intervention involves administering 300 mg of oral gabapentin to patients in the intervention group two hours prior to surgery, aiming to assess its efficacy in attenuating the pressor response to laryngoscopy and tracheal intubation.
Placebo Oral Tablet
The placebo group will receive an identical capsule without active medication, administered two hours before surgery, to compare its effects with those of gabapentin on the pressor response to laryngoscopy and tracheal intubation.
Liaquat National Hospital & Medical College
OTHER