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Evidence of Myogenic Growth Factors in 3D Dynamic Inguinal Hernia Scaffold ProFlor (HERNIA)

U

University of Palermo

Status

Unknown

Conditions

Inguinal Hernia

Treatments

Procedure: Inguinal hernia repair with dynamic prosthesis

Study type

Observational

Funder types

Other

Identifiers

NCT05072171
HERNIA 01_2021

Details and patient eligibility

About

The study utilizes the same tissue specimens gathered for previous investigations and removed from 15 patients already operated for inguinal hernia, who for different reasons needed additional surgery in the previously operated groin.

Full description

Among the individual of investigated the cohort, seven patients underwent groin revision for subsequent hydrocele, 4 for recurrence, and 4 for overlooked ipsilateral multiple hernia protrusions. Made from low weight, large porous polypropylene, ProFlor is composed of a multilamellar cylindrical 3D core, 15 mm thick, with 2 different longitudinal dimensions, 25 or 40 mm. The center of the implant core is connected on one surface to a flat mesh of different width depending on the dimension of the 3D core. This flat part of the device is intended to be deployed to counterface the peritoneal sheath. The 3D core of ProFlor ® is arranged to be compressible on both planes, longitudinal and transversal. Due to its proprietary centrifugal expansion, it can be positioned, fixation free, into the hernia defect for permanent obliteration. ProFlor owns an inherent dynamic responsivity as it contracts and relaxes in accord to the movements of the inguinal floor in which is positioned.

The biopsies were excised from the anterior aspect of the 3D device. It should be noted that once deployed the anterior surface of ProFlor merely faces the external oblique fascia and has no contact with other structures of the groin. Therefore, corruption by host native tissue can be excluded. The biopsies were carried out in ten patients, three in the short term postop. between 3 and 5 weeks, five in the mid-term between 3 and 4 months postop., four in the long-term between 6 and 8 months postop. and the latter three in the extra-long term postop., more than three years after implantation.

Enrollment

15 patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients already operated for inguinal hernia with ProFlor, who for different reasons needed additional surgery in the previously operated groin
  • ASA score >4

Exclusion criteria

  • Patients who do not underwent inguinal hernia repair with ProFlor

Trial design

15 participants in 4 patient groups

Biopsies from 3D hernia scaffold ProFlor in the short term
Description:
3 patients biopsied 3-5 weeks post implantation of ProFlor
Treatment:
Procedure: Inguinal hernia repair with dynamic prosthesis
Biopsies from 3D hernia scaffold ProFlor in the midterm
Description:
5 patients biopsied 3-4 months post implantation of ProFlor
Treatment:
Procedure: Inguinal hernia repair with dynamic prosthesis
Biopsies from 3D hernia scaffold ProFlor in the long term
Description:
4 patients biopsied between 3-4 months post implantation of ProFlor
Treatment:
Procedure: Inguinal hernia repair with dynamic prosthesis
Biopsies from 3D hernia scaffold ProFlor in the extra long term
Description:
3 patients biopsied more than 3 years after implantation of ProFlor
Treatment:
Procedure: Inguinal hernia repair with dynamic prosthesis

Trial contacts and locations

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Data sourced from clinicaltrials.gov

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