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NCT03944291 Clinical Trial

Pudendal Nerve Block for Post-Episiotomy Pain Relief

Pain, Postoperative Clinical Trial

Official title:
Unilateral vs. Bilateral Pudendal Nerve Block for Post-Episiotomy Pain Relief: A Randomized Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03944291
Other study ID # AS1871
Secondary ID
Status Completed
Phase Phase 3
First received
Last updated
Start date May 1, 2019
Est. completion date January 20, 2020

Study information
Verified date January 2020
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Unilateral vs. Bilateral Pudendal Nerve Block for Post-Episiotomy Pain Relief: A Randomized Clinical Trial

Recruitment information / eligibility
Status Completed
Enrollment 102
Est. completion date January 20, 2020
Est. primary completion date January 1, 2020
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- Term (37 to 42 weeks gestation), primigravid women with singleton vertex fetus

Exclusion Criteria:

- Women with bleeding disorders, known hypersensitivity to local anesthetics, chronic use of pain medication, had previous vaginal surgery, extensive vulvovaginal infection, malposition or malpresentation were excluded from the study. Also, women who failed to deliver vaginally, had extensive perineal or cervicat tears, or had instrumental delivery were excluded from the final analysis of the study

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Pudendal Nerve Block
Pudendal Nerve Block

Locations
Country Name City State
Egypt Ain Shams University Maternity Hospital Cairo

Sponsors (1)
Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Visual Analogue Scale for pain scoring visual analogue scale (VAS) from 0 to 100 with 0 corresponding to no pain at all and 100 as the worst pain the woman can describe 48 hours
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