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

U

University of Malaya

Status and phase

Unknown
Phase 3

Conditions

Postoperative Pain
Inguinal Hernia

Treatments

Drug: Pregabalin

Study type

Interventional

Funder types

Other

Identifiers

NCT01450345
toh2c79@Pregabalin

Details and patient eligibility

About

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.

Enrollment

72 estimated patients

Sex

All

Ages

12 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Clinical diagnosis of inguinal hernia
  • Patient undergo operation under daycare basis
  • ASA I-II
  • Written consent

Exclusion criteria

  • ASA > II
  • Allergic reaction against gabapentin and/or pregabalin
  • History of recurrent hernia repair.
  • Patient who has taken analgesia prior to the surgery
  • Liver failure
  • Renal failure
  • Pregnancy

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

72 participants in 1 patient group

Pregabalin Group
Experimental group
Description:
The patient under Group P will be serving with 150 mg of oral Pregabalin 1 to 2 hours prior to induction.
Treatment:
Drug: Pregabalin

Trial contacts and locations

1

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Central trial contact

CharngChee Toh, MBBS, MRCS

Data sourced from clinicaltrials.gov

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