MedTrace Logo

Efficacy of Pre-operative Oral Pregabalin in Ambulatory Inguinal Hernia Repair for Post Operative Pain

NCT01450345 · Status: UNKNOWN · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 72

Last updated 2011-10-12

No results posted yet for this study

Summary

The study carry out is to determine whether the use of oral pregabalin premedication to assess the analgesic efficacy, opiod sparing, adverse effect and clinical value in post-operative pain management.

Conditions

  • Inguinal Hernia
  • Postoperative Pain

Interventions

DRUG

Pregabalin

The patient under Group P will be serving with 150 mg of oral Pregabalin 1 to 2 hours prior to induction.

Sponsors & Collaborators

  • University of Malaya

    lead OTHER

Principal Investigators

  • CharngChee Toh, MBBS, MRCS · University of Malaya

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
12 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-09-30
Primary Completion
2011-12-31
Completion
2011-12-31

Countries

  • Malaysia

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 NCT01450345 on ClinicalTrials.gov