Comparison of postoperative analgesic effects of bilateral rectus sheath block and intravenous patient-controlled analgesia in Total Laparoscopic Hysterectomy

Comparison of postoperative analgesic effects of bilateral rectus sheath block and intravenous patient-controlled analgesia in Total Laparoscopic Hysterectomy: a prospective randomized non-inferiority clinical trial

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0008629

Enrollment

Registered

2023-07-18

Start date

2023-08-02

Completion date

Unknown

Last updated

2023-08-21

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 : - IV PCA group Start by connecting IV PCA (Fentanyl 1500mcg/30ml+Normal saline 70ml, total volume 100ml, bolus 1ml, lock out time 15min, basal 1ml) 30 minutes before the end of sur

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Adult patients undergoing double-port laparoscopic hysterectomy under general anesthesia (aged between 19 and 70 years of age), American Society of Anesthesiologist standard physical condition (ASA class I- III), A person who consented to the clinical trial and signed the subject consent form

Exclusion criteria

Exclusion criteria: Patients who refused rectus sheath block Patients who failed rectus sheath block Patients who refused IV-PCA Patients who have taken opioids for a long time, patients with a history of severe side effects to opioids Patients allergic to local anesthetics Patients with bleeding abnormalities or disorders Those who cannot undergo nerve block due to recent systemic or partial infection Patients who did not undergo hysterectomy using a double port Patients who changed from laparoscopic surgery to open surgery A person who is judged to be inappropriate to participate in a clinical trial according to the judgment of the researcher

Design outcomes

Primary

Measure	Time frame
highest pain score in the recovery room (NRS)	—

Secondary

Measure	Time frame
Resting Pain Score 24 hours after surgery (NRS) ;Pain on movement score 24 hours after surgery (NRS) ;Amount of narcotic analgesic administered;Amount of non-narcotic analgesic administered;First gas-out time after surgery;Frequency of Nausea or Vomiting;Complications in the group that underwent nerve block;Time the patient stopped IV PCA ;Recovery degree questionnaire score after anesthesia;Satisfaction with pain control;sleep satisfaction on the first night after surgery	—

Measure

Time frame

Resting Pain Score 24 hours after surgery (NRS) ;Pain on movement score 24 hours after surgery (NRS) ;Amount of narcotic analgesic administered;Amount of non-narcotic analgesic administered;First gas-out time after surgery;Frequency of Nausea or Vomiting;Complications in the group that underwent nerve block;Time the patient stopped IV PCA ;Recovery degree questionnaire score after anesthesia;Satisfaction with pain control;sleep satisfaction on the first night after surgery

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Countries

Korea, Republic of

Contacts

Public ContactJisun Choi

Samsung Medical Center

luck8909@naver.com+82-2-3410-2470

Outcome results