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the Effect of Dexmedetomidine and Licodaine on Acute Postoperative Pain in Gynecological Laparoscopy

NCT04906889 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2023-01-12

No results posted yet for this study

Summary

The aim of this study is to investigate the effect of opioid-free anesthesia using dexmedetomidine and lidocaine instead of remifentanil infusion, on the acute postoperative pain after the gynecological laparoscopy

Conditions

  • Gynecologic Disease

Interventions

DRUG

Dexmedetomidine Hydrochloride

dexmedetomidine iv bolus for 10 minutes followed by the infusion of 0.1-1 ug/kg/h during general anesthesia

DRUG

Remifentanil Hydrochloride

remifentanil iv infusion of 0.5-5 ng/ml (effect site concentration using TCI) during general anesthesia

DRUG

Lidocaine Hydrochloride

lidocaine iv bolus followed by the infusion of 1.5mg/kg/h during general anesthesia

Sponsors & Collaborators

  • The Catholic University of Korea

    lead OTHER

Principal Investigators

  • Young Eun Moon, MD, PhD · Associate professor, Department of Anesthesiology and Pain Medicine

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
70 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-06-01
Primary Completion
2022-05-30
Completion
2022-06-01

Countries

  • South Korea

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 NCT04906889 on ClinicalTrials.gov