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Perineal Protection Device for Reducing Perineal Trauma During Vaginal Delivery in First-time Mothers: a Multicenter Randomized Controlled Trial

Study acronym: PeriPROTECT
StatusNot Yet Recruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

  1. Minor Study First Submitted
149 trials monitored
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The goal of this clinical trial is to determine whether using a soft perineal protection device (BabySlide®) in addition to standard manual perineal support during vaginal delivery can reduce the risk of perineal trauma in first-time mothers. The main questions it aims to answer are: Does the use of BabySlide® reduce the risk of obstetric anal sphincter injury (OASI)? Does the use of BabySlide® reduce the risk of second-, third-, or fourth-degree perineal tears and/or episiotomy? Researchers will compare women randomized to receive BabySlide® in addition to standard manual perineal support with women receiving standard manual perineal support alone to determine whether the device reduces perineal trauma during vaginal delivery. Participants will: be randomized during the late second stage of labour to either BabySlide® plus standard manual perineal support or standard manual perineal support alone; receive the allocated perineal protection method during vaginal delivery; have perineal outcomes assessed and documented after delivery; and complete follow-up assessments and questionnaires after delivery to evaluate recovery and pelvic floor symptoms.
Trial Details
NCT Number NCT07862660
Lead Sponsor Region Skane
Collaborators: Clinical Studies Sweden - Forum South
Conditions
(from sponsor)
Pelvic Floor Dysfunction, Perineal Laceration, Wound Dehiscence, Anal Incontinence, Sexual Dysfunction and the Mode of Deliveries, Perineal Injury, Perineal Infection, Perineal Pain +2 more
Related terms Encopresis, Pelvic Organ Prolapse, Sexual Dysfunction, Physiological
Enrollment 4,226 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov