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Effect of Preoperative Rectus Sheath Block on Quality of Recovery in Single Port Laparoscopic Adnexal Surgery

NCT05984212 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 56

Last updated 2023-08-09

No results posted yet for this study

Summary

In this study, the investigators aimed to demonstrate if the quality of recovery in patients undergoing single-port laparoscopic adnexal surgery, with preoperative rectus sheath block and intraoperative opioid administration based on analgesia nociception index, improves compared to the patients without block.

Conditions

  • Single Port Laparoscopic Adnexal Surgery

Interventions

DRUG

Ultrasound guided rectus sheath block with dexmedetomidine

Intervention Group: Ultrasound guided rectus sheath block with 0.5% ropivacaine 20ml at each side (bilateral)

DRUG

Ultrasound guided rectus sheath block with normal saline

Control Group: Ultrasound guided rectus sheath block with 0.9% normal saline 20ml at each side (bilateral)

Sponsors & Collaborators

  • Yonsei University

    lead OTHER

Principal Investigators

  • Youngwon Kim · Department of Anesthesiology and Pain Medicine, Anesthesia and Pain Research Institute, Yonsei University College of Medicine

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
19 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-08-31
Primary Completion
2024-07-31
Completion
2024-07-31

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 NCT05984212 on ClinicalTrials.gov