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Recruiting Not applicable

Superior HypogastrIc plExus bLock During Laparoscopic Colorectal Cancer Surgery

NCT07579780 · tracked via the Priya Life Science China tracker
Phase
Not applicable
Started
2025-12-15
Last updated
2026-05-12

Condition(s) studied

Colorectal Cancer (Diagnosis)Laparoscopic SurgerySuperior Hypogastric Plexus Block

Investigational drug(s) / intervention(s)

Superior hypogastric plexus block

Superior hypogastric plexus block: After establishing pneumoperitoneum in laparoscopic colorectal cancer surgery, the superior hypogastric plexus block will be performed on all patients. The block will contain 20 mL of 0.75% ropivacaine hydrochloride or 0.9% normal saline. The injection will be performed by tenting the presacral peritoneum, aspirating with a laparoscopic needle-tip syringe to ensure extravascular placement, and injecting the block.

Study summary

This trial seeks to assess the efficacy of a superior hypogastric plexus block for early quality of recovery after laparoscopic colorectal cancer surgery.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Able to provide informed consent. * Undergoing elective laparoscopic radical resection for colorectal cancer. * American Society of Anesthesiologists Physical Status (ASA) class I-III. Exclusion Criteria: * Allergy to block medication (s). * Coagulation dysfunction. * Local or systemic infection. * Unable to cooperate with the completion of the study protocol.

Primary outcome measure(s)

  • Quality of recovery — Up to postoperative day 2
    The Quality of recovery (QoR) 15, ranging from 0 (the worst) to 150 (the best), is a patient-reported outcome questionnaire that measures the quality of recovery after surgery.

Trial sites (1)

FacilityCityRegionStatus
The Sixth Affiliated Hospital of Sun Yet-set University Guangzhou Guangdong Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07579780 on ClinicalTrials.gov ↗ ← All trials in China