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NCT01461031 Clinical Trial

Effect of Nefopam on Acute Postoperative Pain in Patients Undergoing Orthognathic Surgery

Pain Clinical Trial

Official title:
Effect of Nefopam on Acute Postoperative Pain in Patients Undergoing Orthognathic Surgery

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01461031
Other study ID # nefopam-orthognathic
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 2011
Est. completion date September 2012

Study information
Verified date February 2021
Source The Catholic University of Korea
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to determine the analgesic effect of perioperative nefopam on acute pain in patient undergoing orthognathic surgery.

Recruitment information / eligibility
Status Completed
Enrollment 40
Est. completion date September 2012
Est. primary completion date September 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 60 Years
Eligibility Inclusion Criteria: - aged 20-60 years - undergoing elective orthognathic surgery Exclusion Criteria: - pregnancy - psychiatric disease - hepatobiliary or renal disease - monoamine oxidase inhibitor-taking patients

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• nefopam
nefopam infusion for postoperative 24 hours
• normal saline (control)
normal saline infusion for postoperative 24 hours

Locations
Country Name City State
Korea, Republic of Seoul St.Mary's Hospital Seoul Seocho-gu

Sponsors (1)
Lead Sponsor Collaborator
The Catholic University of Korea

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary pain score on the visual analogue scale after orthognathic surgery (up to postoperative 24 hours)
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