Presacral Nerve Block Versus Sham Block on Post-operative Pain for Total Laparoscopic Hysterectomy

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexFemale
Age18+
SponsorMount Sinai Hospital, Canada

About this trial

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.

Eligibility criteria

Qualifiers

18 years of age or older

Undergoing total laparoscopic hysterectomy

Disqualifiers

Previous presacral neurectomy

Concurrent surgical procedure other than salpingectomy and/or oophorectomy

Gynecological cancer beyond stage 1 disease

BMI > 50

Trial design

Treatments tested in this trial

  • Ropivacaine injection
  • Normal saline injection

Treatment groups

60 Participants
are divided into 2 treatment groups

Locations

1
Mount Sinai HospitalM5G 1X5, TorontoOntario, Canada

Sponsors and collaborators

Mount Sinai Hospital, Canada

Lead sponsor