Viewing Study NCT02561494


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Study NCT ID: NCT02561494
Status: COMPLETED
Last Update Posted: 2016-10-28
First Post: 2015-08-02
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Postoperative Analgesic Effect of Nefopam
Sponsor: Seoul National University Bundang Hospital
Organization:

Study Overview

Official Title: None
Status: COMPLETED
Status Verified Date: 2016-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Nefopam will be administered to the patients undergoing laparoscopic gastrectomy under the total intravenous anesthesia (TIVA).

The investigators will evaluate whether the nefopam can decrease the total amount of remifentanil administered during the operation, which will reduce the acute opioid tolerance and following consumption of fentanyl during postoperative period.
Detailed Description: None

Study Oversight

Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?: