NCT03939910

Effect of Preemptive Pudendal Nerve Block Using Bupivacaine Versus Ropivacaine on Post-operative Pain After Posterior Vaginal Repair.

Status unknown NA Last updated 7 May 2019

What this trial tests

NA trial testing Pudendal Nerve Block needle in pre-packaged kits that include both the trumpet and the needle. The needle will limits its depth of penetration to 5 mm beyond the trumpet. in Post-operative Pain After Posterior Vaginal Repair in 72 participants. Status unknown.

Timeline

1 June 2019

Primary endpoint
30 December 2020

30 June 2021

Quick facts

Lead sponsor	Munazzah Rafique
Phase	NA
Status	Status unknown
Study type	INTERVENTIONAL
Allocation	randomized
Design	parallel
Masking	quadruple
Primary purpose	prevention
Enrollment	72
Start date	1 June 2019
Primary completion	30 December 2020
Estimated completion	30 June 2021

Drugs / interventions tested

• Pudendal Nerve Block needle in pre-packaged kits that include both the trumpet and the needle. The needle will limits its depth of penetration to 5 mm beyond the trumpet.

Conditions studied

• Post-operative Pain After Posterior Vaginal Repair — all drugs for Post-operative Pain After Posterior Vaginal Repair →

Sponsor

Munazzah Rafique

Who can join

Adults 20 to 80, female only, with Post-operative Pain After Posterior Vaginal Repair. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To investigate the efficacy of preemptive pudendal nerve blockade on postoperative pain, after posterior vaginal repair, below the level of ischial spine, excluding uterine suspension procedures that are higher than the coverage of the block.

Primary outcome:

The primary outcome measures of the study visual analogue pain scores and postoperative analgesic consumption.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.