Effect of Preoperative Rectus Sheath Block on Quality of Recovery in Single Port Laparoscopic Adnexal Surgery: A randomized controlled trial

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0011467

Enrollment

Registered

2026-01-15

Start date

2023-08-10

Completion date

Unknown

Last updated

2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Procedure/Surgery : Intervention Group: Ultrasound guided rectus sheath block with 0.5% ropivacaine 20ml at each side (bilateral) Control Group: Ultrasound guided rectus sheath block with 0.9% normal

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Adult female patient aged 19 years or older undergoing regular single-port laparoscopic adnexal surgery under general anesthesia at Yonsei Cancer Center

Exclusion criteria

Exclusion criteria: patients with moderate to severe pain before surgery, patients with a history of taking chronic pain medications before surgery, patients with a history of allergy or hypersensitivity to remifentanil or a local anesthetic (ropivacaine), patients with an infection at the site where your block will be performed, patients who cannot communicate

Design outcomes

Primary

Measure	Time frame
24hours postoperative QoR-15 scale score	—

Secondary

Measure	Time frame
intraoperative remifentanil consumption;Pain scores at 0, 1, 6, 12, and 24 hours after surgery;Rescue analgesic consumption for postoperative 24 hours;patients' satisfaction on pain control at postoperative 24hours;incidence and severity of postoperative nausea and vomiting ; serum cortisol level, leukocyte level, arterial pH, blood glucose level	—

Countries

Korea, Republic of

Contacts

Public ContactYoungwon Kim

Yonsei University Health System, Severance Hospital

youngwon.md@gmail.com+82-2-6091-6849

Outcome results