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Simple Continuous, Subcuticular and Interrupted Skin Suturing of Episiotomy and 2nd-degree Perineal Tears

A

Assiut University

Status

Unknown

Conditions

Episiotomy Wound

Treatments

Procedure: Episiotomy

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Millions of women worldwide undergo perineal suturing after childbirth and the type of repair may have an impact on pain and healing.

The skin as a barrier between the internal structures and the external environment is exceptionally susceptible to injury, either through accidental injury or planned surgical incision. Today, as surgery increases in complexity, and the heightened public awareness of scar cosmesis and skin healing need to be optimized to ensure the overall success of the surgical procedure

Enrollment

138 estimated patients

Sex

Female

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Normal vaginal delivery.
  • At term (37 40 weeks ).
  • Live baby.
  • Vertex presentation

Exclusion criteria

  • Third and fourth degree perineal tear.
  • Instrumental vaginal delivery.
  • Previous perineal surgery.
  • Anaemia with hemoglobin level < 9 g/dl.
  • Diabetes mellitus.
  • Coagulation abnormalities.
  • Postpartum hemorrhage.
  • Delivery conducted outside Woman HealthHospital.
  • Breech delivery.
  • Body mass index >35 kg/m2.
  • Local infectious lesions.
  • Anal fissures or hemorrhoid.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

138 participants in 3 patient groups

Simple continuous
Experimental group
Description:
the sutures will be taken continuously by simple method
Treatment:
Procedure: Episiotomy
subcuticular
Active Comparator group
Description:
the sutures will be taken subcuticular
Treatment:
Procedure: Episiotomy
interrupted
Active Comparator group
Description:
the sutures will be taken interrupted method
Treatment:
Procedure: Episiotomy

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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