Status:

COMPLETED

Preemptive Oral Gabapentin 600 mg in Reducing Morphine Requirement After Non Obstetric Lower Abdominal Surgery

Lead Sponsor:

Indonesia University

Conditions:

Non-obstetric Lower Abdominal Surgery

Eligibility:

All Genders

18-65 years

Phase:

PHASE1

PHASE2

Brief Summary

This study aimed to get the information about the effectiveness of preemptive oral gabapentin 600 mg in reducing morphine requirement after non obstetric lower abdominal surgery

Detailed Description

Seventy-two subjects were given informed consent before enrolling the study and randomized into two groups; gabapentin and placebo. Two hours before the incision, patients were given preemptive analge...

Eligibility Criteria

Inclusion

  • Inclusion criteria:
  • Male or female
  • Age: 18-65 years old
  • Weigh in range around 20% of the ideal body weight
  • Physical status ASA I-II
  • Scheduled for elective non-obstetric lower abdominal surgery with general anesthesia
  • Duration of surgery less than 4 hours
  • Patients who agreed to participate in this study and sign informed consent
  • Exclusion criteria:
  • Patients who have history of allergy or hypersensitivity to gabapentin, paracetamol, morphine, or the other opioids
  • Patients who consumed analgesia and NSAID less than 12 hours before surgery
  • Patients who experienced physical trauma less than 4 days before surgery
  • Patients who have contraindications to gabapentin, morphine, and paracetamol
  • Patients who were treated with neuraxial block or peripheral nerve block before and during surgery
  • Patients who have history of diabetes, severe live or renal disease
  • Patients who were treated with antihypertension, sedatives, hypnotics, antidepressants, and the other drugs that have effects on nervous system
  • Patients who have psychiatric disorders
  • Patients who consumed gabapentin before perioperative period
  • Pregnant or breastfeeding patients

Exclusion

    Key Trial Info

    Start Date :

    November 11 2019

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    February 29 2020

    Estimated Enrollment :

    72 Patients enrolled

    Trial Details

    Trial ID

    NCT04434430

    Start Date

    November 11 2019

    End Date

    February 29 2020

    Last Update

    September 13 2021

    Active Locations (1)

    Enter a location and click search to find clinical trials sorted by distance.

    Page 1 of 1 (1 locations)

    1

    Cipto Mangunkusumo Cental National Hospital

    Jakarta, DKI Jakarta, Indonesia, 10430