MedTrace Logo

Preemptive Oral Gabapentin and Tramadol on Postoperative Pain After Knee Arthroscopy

NCT06112223 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2024-10-02

No results posted yet for this study

Summary

The aim of this study to evaluate the effect of preemptive oral gabapentin versus tramadol on postoperative pain after knee arthroscopy under spinal anesthesia.

Conditions

  • Gabapentin
  • Tramadol
  • Postoperative Pain
  • Knee Arthroscopy
  • Spinal Anesthesia

Interventions

DRUG

Gabapentin

Patients will receive oral gabapentin 600 mg 1 hour before the surgery.

DRUG

Tramadol

Patients will receive oral tramadol 100 mg 1 hour before the surgery.

Sponsors & Collaborators

  • Tanta University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-04-01
Primary Completion
2023-09-01
Completion
2023-09-01

Countries

  • Egypt

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06112223 on ClinicalTrials.gov