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Spots Global Cancer Trial Database for Postoperative Analgesic Effect of Nefopam

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Trial Identification

Brief Title: Postoperative Analgesic Effect of Nefopam

Official Title:

Study ID: NCT02561494

Interventions

Nefopam
Saline

Study Description

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:

Keywords

Eligibility

Minimum Age: 20 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Seoul National University Bundang Hospital, Seongnam, Gyeonggi, Korea, Republic of

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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