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Incidence Of Mesh Infection After Hernioplasty In Obstructed and Strangulated Hernia Using Proline Mesh and Sutures

A

Assiut University

Status

Not yet enrolling

Conditions

Incidence of Mesh Infection In Hernioplasty

Treatments

Procedure: Proline mesh in hernioplasty

Study type

Interventional

Funder types

Other

Identifiers

NCT05775276
Incidence Of Mesh Infection

Details and patient eligibility

About

The primary aim of this study is to detect incidence of mesh infection in cases presented with obstructed or strandulated hernia.A prospective controlled study will be carried out after obtaining written informed consent from all patients and approval of the ethics committee of the faculty of medicine, Assuit University.

Full description

There is controversy regarding the use of prolene mesh in cases of obstructed and strangulated hernia. The main aim and objective of this prospective study is to evaluate the outcomes and incidence of mesh infection in hernioplasty in emergency situations like obstructed and strangulated hernia .Hernioplasty is the most common surgery for hernia repair with Propylene mesh,but the use of synthetic prosthesis is associated with increase risk of developing a prosthetic infection that may manifest after time as subtle symptoms in the form of fever, myalgia, erythema of overlying skin and in some cases as chronic discharging sinus(1). clinicians have been challenged in the past few years by an increasing variety of novel non-infectious and infectious complications following the widespread use of meshes after open repair of hernias this incidence is influenced by underlying co-morbidities, the type of mesh, the surgical technique and the strategy used to prevent infections. An approach that combines medical and surgical management is necessary for cases of mesh infection.(2)

Enrollment

60 estimated patients

Sex

All

Ages

21+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All adult patients aging above 21 years old, who presented with obstructed or strangulated hernia with viable bowel loops by clinical examination or detected by preoperative ultrasound or computed tomography CT imaging.

Exclusion criteria

  • Uncomplicated hernia.
  • patients who will underwent rescection and anastmosis
  • patient cannot withstand anethesia.
  • Decompensated liver patients.
  • Pregnancy.
  • Immunosuppressed patients e.g.: under chemotherapy or steroids.

Trial design

Primary purpose

Screening

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

60 participants in 1 patient group

Incidence Of Mesh Infection After proline mesh Hernioplasty
Experimental group
Description:
Cases presented with strangulated or obstructed hernia
Treatment:
Procedure: Proline mesh in hernioplasty

Trial contacts and locations

0

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Central trial contact

Mohamed Sayed

Data sourced from clinicaltrials.gov

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