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

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Yonsei University

Status

Not yet enrolling

Conditions

Single Port Laparoscopic Adnexal Surgery

Treatments

Drug: Ultrasound guided rectus sheath block with dexmedetomidine
Drug: Ultrasound guided rectus sheath block with normal saline

Study type

Interventional

Funder types

Other

Identifiers

NCT05984212
4-2023-0611

Details and patient eligibility

About

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.

Enrollment

56 estimated patients

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  1. Adult female patient aged 19 years or older undergoing elective single-port laparoscopic adnexal surgery under general anesthesia at Yonsei Cancer Center

  2. patients with moderate to severe pain before surgery 2. patients with history of taking chronic analgesic use, 3. patients allergic or hypersensite to remifentanil or local anesthetic (ropivacaine), 4. patients with infection at the site of the block, 5. patietns who cannot communicate

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

56 participants in 2 patient groups, including a placebo group

dexmedetomidine infusion group
Experimental group
Treatment:
Drug: Ultrasound guided rectus sheath block with dexmedetomidine
normal saline infusion group
Placebo Comparator group
Treatment:
Drug: Ultrasound guided rectus sheath block with normal saline

Trial contacts and locations

1

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Central trial contact

Youngwon Kim

Data sourced from clinicaltrials.gov

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