KCT0008629RecruitingUnknown
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
Conditions
Trial Snapshot
- Phase
- Unknown
- Status
- Recruiting
- Sponsor
- Samsung Medical Center
- Enrollment
- 76
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 19(Year) to 70(Year) (—)
- Sex
- Female
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
- •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
Investigators
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