Gabapentin and Pressor Response to Intubation

PHASE1/PHASE2Not yet recruitingINTERVENTIONAL
Enrollment

144

Participants

Timeline

Start Date

December 15, 2024

Primary Completion Date

June 15, 2025

Study Completion Date

July 16, 2025

Conditions
Elective Surgical PatientsBlood Pressure
Interventions
DRUG

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.

OTHER

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.

All Listed Sponsors
lead

Liaquat National Hospital & Medical College

OTHER

NCT06705101 - Gabapentin and Pressor Response to Intubation | Biotech Hunter | Biotech Hunter