MedTrace Logo

The Effect of the Modified Perineal Protection Device During Delivery

NCT02013752 · Status: UNKNOWN · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2015-03-19

No results posted yet for this study

Summary

The purpose of this study is to determine whether a modified perineum protection device can reduce tearing during delivery.

Conditions

  • Perineal Tears.

Interventions

DEVICE

Perineal protection device.

A device used to reduce perineal tears during delivery of the baby.

Sponsors & Collaborators

  • Knut Haadem

    lead OTHER

Principal Investigators

  • Knut Haadem, M.D., PhD · Campus Helsingborg, Clinical Science Faculty of Medicine, Lund University, Helsingborg, Sweden

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-03-31
Primary Completion
2015-09-30
Completion
2015-12-31

Countries

  • Sweden

Study Locations

More Related Trials

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 NCT02013752 on ClinicalTrials.gov