NCT06455540Not yet recruitingNot Applicable
Superior Hypogastric Plexus Block During Laparoscopic Hysterectomy
Sixth Affiliated Hospital, Sun Yat-sen University0 sites198 target enrollmentStarted: July 16, 2024Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 198
- Primary Endpoint
- Quality of recovery
Study Overview
Brief Summary
This trial sest to assess the efficacy of a superior hypogastric plexus block (SHPB) for quality of recovery after a laparoscopic hysterectomy.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Prevention
- Masking
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Eligibility Criteria
- Ages
- 18 Years to 70 Years (Adult, Older Adult)
- Sex
- Female
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Able to provide informed consent
- •Undergoing laparoscopic hysterectomy for benign indications
Exclusion Criteria
- •Planned procedure that requires dissection of the presacral space
- •Allergy to block medication (s)
- •Known or suspected malignancy
Outcomes
Primary Outcomes
Quality of recovery
Time Frame: Postoperative day 1
The Quality of recovery (QoR) 15 is a patient-reported outcome questionnaire that measures the quality of recovery after surgery.
Secondary Outcomes
- The McGill Pain Questionnaire(Up to postoperative day 90)
- Postoperative Pain Scores(Up to postoperative day 2)
- Postoperative Opioid Use(Up to postoperative day 2)
- Quality of recovery(Up to postoperative day 2)
- Postoperative nausea and vomiting(Up to postoperative day 2)
- The Brief Pain Inventory (BPI)(Up to postoperative day 90)
- Incidence of Adverse events(Intraoperative (During block performance))
- Length of stay in post-anesthesia care unit (PACU) area(Postoperative day 1)
Investigators
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