Presacral Nerve Block Versus Sham Block on Post-operative Pain for Total Laparoscopic Hysterectomy
Study Details
Study Description
Brief Summary
The study is a single-center parallel group randomized controlled trial comparing the administration of a presacral nerve block using 20mL of local ropivacaine 5.0mg/ml versus 20mL of normal saline (sham block) on post-operative pain following total laparoscopic hysterectomy.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 2 |
Detailed Description
The proposed study is a single-center parallel group RCT comparing the administration of a presacral nerve block using 20mL of local ropivacaine 5.0mg/ml versus 20mL of normal saline (sham block). This drug/dose was selected based on the recent study by Rapp et al. who instilled 20mL of ropivacaine into the presacral nerve at the time of open hysterectomy. Participants will be selected using a convenience sample from Mount Sinai Hospital's outpatient gynecology clinics. All patients > or = age 18 years undergoing total laparoscopic hysterectomy will be considered for this study. Exclusion criteria include: previous presacral neurectomy, concurrent surgical procedure other than salpingectomy and/or oophorectomy, gynecological cancer beyond stage 1 disease, chronic opioid consumption, fibromyalgia, BMI >50, language barrier, inability to communicate and inability to provide consent. All potentially eligible patients will be invited to participate in this study by their surgeon. Interested patients will then meet with a member of the research team to explain the study and obtain consent.
The investigators will create a randomization list using a computer-generated allocation sequence in equal ratio with study numbers 1 to 60. Our clinic nurse, who works 5 days per week in our ambulatory office and who will have no other role in this study, will prepare the active and placebo syringes and label the syringes according to the randomization list. Each syringe will be prepared individually and provided to the surgeon on the day of surgery.
Study participants will be randomized on the day of surgery. The surgeon will instill the drug/placebo from the labeled syringe into the presacral space as the first step prior to starting the hysterectomy.
The surgeon, research team, participants and data analysts will be blinded to treatment group.
Each study patient will receive standardized perioperative care as follows:
All patients will receive preoperative multimodal analgesia with acetaminophen 1000 mg.
A protocolized general anesthetic will be used for all patients. Induction of anesthesia will be performed with fentanyl (1-3 mcg/kg), propofol (2-3 mg/kg), and rocuronium (0.6 mg/kg), followed by endotracheal intubation. Patients will be maintained with Sevoflurane anesthetic titrated to a minimum alveolar concentration (MAC) of 0.9-1.2 in a mixture of 50:50 air/oxygen. Analgesia will be provided with intravenous fentanyl and/or hydromorphone administered to maintain mean arterial pressure or heart rate within 20% of baseline measurements. At skin closure, unless contraindicated, all patients will be administered intravenously ondansetron 4 mg and IV dexamethasone 0.1 mg/kg for nausea prophylaxis. Unless contraindicated, all patients will also receive intravenous ketorolac 30 mg for analgesia. Local anesthetic will be provided at the site of the port incisions (2ml per port site of 0.25% bupivacaine with epinephrine). Following completion of surgery, neuromuscular blockade will be antagonized with neostigmine and glycopyrrolate, and patients will be extubated and brought to the post anesthesia care unit (PACU). As per protocol and routine care, the only adjunctive analgesic administered intra-operatively in addition to opioids will be intravenous ketorolac.
Post-operative pain scores will be assessed using a self-administered numeric rating scale (NRS) for pain at 1, 2 and 3 hours after arrival in the PACU. Those patients with pain scores > 4/10 will receive analgesia according to a standard postoperative analgesic regimen. This will consist of intravenous fentanyl 25-50 mcg boluses every 5-10 minutes, intravenous administration of hydromorphone 0.2-0.4 mg boluses as required, and oral administration of either hydromorphone IR 1-2 mg or oxycodone IR 5-10 mg.
Rescue antiemetics will be administered if required at the discretion of the anesthesiologist in the form of IV metoclopramide 5-10 mg, ondansetron 4 mg, or dimenhydrinate 25-50 mg.
Patients will be contacted post-operatively days 1, 2 and 7 in order to assess post-operative pain scores, calculate total opioid consumption and elicit any adverse events (secondary outcomes).
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Presacral Nerve Block Presacral nerve block using 20mL of local ropivacaine 5.0mg/ml instilled in the presacral space |
Drug: Ropivacaine injection
Presacral nerve block using 20mL of local ropivacaine 5.0mg/ml
Other Names:
|
| Sham Comparator: Sham Block 20mL of normal saline (sham block) instilled in the presacral space |
Drug: Normal saline injection
Sham block using 20 mL of normal saline
Other Names:
|
Outcome Measures
Primary Outcome Measures
- Early post-operative pain at 3 hours following surgery [3 hours following surgery]
Early post-operative pain measured at 3-hours following surgery by a self-administered numeric pain rating scale (NRS) on a scale from 0 to 10, with 0 indicating no pain and 10 indicating the worst pain imaginable
Secondary Outcome Measures
- Post-operative pain at other time points [1 hour, 2 hour, and post-operative days 1, 2 and 7]
Delayed post-operative pain measured by NRS scores at 1 hour, 2 hour, and post-operative days 1, 2 and 7 on a scale from 0 to 10, with 0 indicating no pain and 10 indicating the worst pain imaginable
Other Outcome Measures
- Post-operative narcotic usage [Post-operative days 1, 2 and 7]
Total narcotics administered from end of surgery until post-operative days 1, 2 and 7 (calculated from the hospital medical records and pill counts from discharge medications to be elicited by phone the day after surgery)
- Adverse effects/complication rates [Post-operative days 1, 2 and 7]
Any negative outcome that is self-reported and elicited from a telephone survey
Eligibility Criteria
Criteria
Inclusion Criteria:
-
18 years of age or older
-
Undergoing total laparoscopic hysterectomy
Exclusion Criteria:
-
Previous presacral neurectomy
-
Concurrent surgical procedure other than salpingectomy and/or oophorectomy
-
Gynecological cancer beyond stage 1 disease
-
BMI > 50
-
Chronic opioid consumption
-
Fibromyalgia
-
Language barrier
-
Inability to communicate and provide consent
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- Mount Sinai Hospital, Canada
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- REB# 21-0104-A