None listed
Conditions
Brief summary
This study is testing whether a targeted nerve block performed during laparoscopic surgery can help reduce pelvic pain after surgery in women with endometriosis. The nerve block, called a Superior Hypogastric Plexus (SHP) block, is a low-risk anaesthetic injection given while the patient is asleep during surgery. The goal is to see if it reduces the need for strong pain medications like opioids and improves recovery. The study will compare two groups: one receiving the SHP block and one receiving a placebo injection. We believe the SHP block group will have lower pain scores and require fewer medications after surgery.
Interventions
Intervention Name: Arm 1 – SHP Block: Intraoperative Superior Hypogastric Plexus (SHP) block with local anaesthetic Arm 2 – Placebo Control: Intraoperative sham injection with normal saline Intervention Description (Arm 1 – SHP Block) Brief name: Intraoperative Superior Hypogastric Plexus (SHP) block with 0.25% bupivacaine Materials: Standard surgical supplies, including 10–20 mL of 0.25% bupivacaine, 22G spinal needle, and syringes. No additional patient-facing materials are used. Procedures: After induction of general anaesthesia, participants randomised to the intervention group will receive an SHP block performed under direct laparoscopic visualisation. Using a 22G spinal needle, the surgeon will inject 10–20 mL of 0.25% bupivacaine into the retroperitoneal space at the location of the superior hypogastric plexus, typically just inferior to the aortic bifurcation, anterior to the L5 vertebral body. Provider and expertise: Administered by a consultant gynaecological laparoscopic surgeon or a trained fellow with experience in pelvic nerve blocks under supervision. Mode of delivery: Face-to-face during surgery under general anaesthesia. Delivered individually to each participant. Timing and dose: A single dose of bupivacaine (10–20 mL of 0.25%) is administered once intraoperatively. Location: Operating theatres at Mater Mothers Hospital, Brisbane, within the Advanced Laparoscopy Gynaecological Unit. Adaptation: The intervention is not titrated or adapted. Standard volume and technique are used in all patients. Fidelity and adherence: Fidelity will be assessed by surgical documentation, intraoperative photography, and adherence to the standardised SHP block protocol. Fidelity checks will be conducted periodically by the principal investigator.
Sponsors
Study design
Eligibility
Inclusion criteria
Female patients aged 18 to 50 years Undergoing operative laparoscopy for confirmed or suspected endometriosis History of chronic pelvic pain (greater than or equal to 6 months duration) ASA physical status classification I–II Willing and able to provide written informed consent Fluent in English or able to complete questionnaires with assistance
Exclusion criteria
Known allergy or hypersensitivity to local anaesthetics (e.g. bupivacaine) Previous pelvic nerve block or pelvic surgery within the last 6 months Coagulopathy or current use of anticoagulant medications Severe pelvic adhesions precluding safe SHP block administration Pregnancy or breastfeeding at time of surgery Inability or unwillingness to provide informed consent