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Comparison of Lornoxicam and Paracetamol for Pre-emptive Intravenous Analgesia for Elective Inguinal Hernia Repair

NCT01069055 · Status: UNKNOWN · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2010-02-24

No results posted yet for this study

Summary

The purpose of this study is to determine whether lornoxicam or paracetamol is more effective in providing pre-emptive analgesia for adult patients undergoing elective unilateral inguinal hernia repair under general anesthesia.

Conditions

  • Inguinal Hernia
  • Postoperative Pain

Interventions

OTHER

Sterile Saline

Group I: 100 ml intravenous saline infusion as placebo 30 minitues before the surgery.

DRUG

Intravenous lornoxicam

Group II: 8 mg intravenous lornoxicam infusion in 100 ml saline 30 minitues before the surgery.

DRUG

Intravenous paracetamol

Group III: 1 g intravenous paracetamol infusion in 100 ml saline 30 minitues before the surgery.

Sponsors & Collaborators

  • Diskapi Teaching and Research Hospital

    lead OTHER

Principal Investigators

  • Ercan Sonmez, MD · Diskapi Teaching and Research Hospital

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-02-28
Primary Completion
2010-06-30
Completion
2010-06-30

Countries

  • Turkey (Türkiye)

Study Locations

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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 NCT01069055 on ClinicalTrials.gov