Single dose of intravenous paracetamol versus placebo in post-orthognathic surgery pain: A randomized clinical trial

Phase 4

Completed

• Conditions: orthognathic surgery patients; intravenous paracetamol; orthognathic surgery

• Registration Number: TCTR20210908002
• Lead Sponsor: Faculty of Dentistry, Chulalongkorn University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2021-09-08
• Study Completion: 2022-11-30
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 62

Inclusion Criteria

1. patient undergoing orthognathic surgery
2. ASA classification 1 or 2

Exclusion Criteria

1. Allergy to drug used in the trial.
2. Patient refusal.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
pain every 4 hour in first 24 hour post operation visual analogue pain score

Secondary Outcome Measures

Name	Time	Method
morphine consumption and side effect at 24 hour post operation observation