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The Effect of Perineal Protective Package Application on Pelvic Floor in Labor

NCT06428812 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2025-06-17

No results posted yet for this study

Summary

This study aimed to evaluate the effect of perineal protection package application on labor outcomes, perineal integrity, postpartum urinary incontinence and pelvic floor muscle strength.In this study, a package including practices that have been proven to protect the perineum in labor was created and it was aimed to examine the effect of this perineal protection package; as a whole. The;perineal protective package; applications created by the researchers consisted of positioning on the gynecologic table (the back of the table was erected, the legs were removed from the hooks and placed on the sides of the table), open glottis pushing instead of closed glottis pushing, hot compress protection of the perineum instead of dry compress protection of the perineum, instead of lithotomy position in the second stage, which reduces the tension of the perineum and allows it to be observed and protected manually.

Conditions

  • Pregnancy
  • Labor
  • Pelvic Floor

Interventions

OTHER

Experimental: perineal package application group

This group includes those in the 2nd stage of labor upright position spontaneous pushing Hot application will be made

Sponsors & Collaborators

  • Öznur Hayat Öktem

    lead OTHER

Principal Investigators

  • Nazan KARAHAN, Associate professor · Gulhane School of Medicine

  • MEHMET BÜLBÜL, Associate professor · Karabuk University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
35 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-07-08
Primary Completion
2025-03-11
Completion
2025-03-11

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06428812 on ClinicalTrials.gov