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Minimally Invasive Techniques in Ventral Hernioplasty

A

Assiut University

Status

Not yet enrolling

Conditions

Ventral Hernia

Treatments

Procedure: ventral hernia repair

Study type

Interventional

Funder types

Other

Identifiers

NCT06255314
laparoscopic ventral hernia

Details and patient eligibility

About

  1. Review the surgical outcome of different techniques using extraperitoneal ventral hernia repair regarding postoperative pain. wound infection ,hospital stay , recurrence ,mesh migration and mesh induced visceral complications.
  2. Reviewing advantages and drawbacks of each surgical technique regarding feasibility ,cost effectiveness and technical difficulties

Full description

The laparoscopic ventral hernia repair was first introduced by LeBlanc and Booth in the early 1990s . Since its introduction, it has continued to evolve and has become an important option in the hernia surgeon's armamentarium. However, only 27.4% of ventral hernia repairs are performed laparoscopically, likely because of the relatively advanced nature of this procedure and because all hernias may not be suitable for a laparoscopic approach. Using current techniques, numerous studies have documented the safety and efficacy of this approach. Some data suggest that the laparoscopic approach results in a shorter hospital stay and lower recurrence rates compared with open approaches. However, pain may still be significant after laparoscopic repairs and there are not significant advantages from this standpoint. Nonetheless, it is well accepted that the primary advantage of the laparoscopic approach is that wound infections are less frequent compared with open approaches .LeBlanc and Booth in 1993 first reported application of intra-peritoneal onlay mesh (IPOM) for ventral and incisional hernia, However the technique requires expensive fixation devices which may cause acute and chronic pain .The laparoscopic groin hernia repair using synthetic mesh in TEP or TAPP are acceptable surgical techniques today These techniques are rarely associated with mesh induced complications, the reason being extraperitoneal placement of synthetic mesh. It is apparent that despite great progress in mesh technology, nearly all types of meshes have been found to produce a varying level of adhesion or tissue reaction, regardless of the material and coating used. Preoperatively unpredictable, a mesh-induced visceral complication may occur in some patients to produce severe reaction or major mesh-related adverse events.The incitation to develop certain novel minimally invasive techniques that enables researchers to bring the mesh out of abdominal cavity has been an exciting trend in laparoscopic hernia repair.

Enrollment

45 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • • Able to give informed consent for inclusion in the study

    • Age of the patient : above 18 years
    • Any type of ventral hernia including umbilical,paraumbilical,epigastric,spigelian and incisional hernias

Exclusion criteria

  • • Patients with inguinal hernia.

    • Strangulated or obstructed hernia.
    • Previous mesh hernia repair.
    • Loss of abdominal domain.
    • Infected or contaminated field.
    • Defect size more than 10cm.

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

45 participants in 3 patient groups

trans abdominal retromusclar laparoscopic ventral hernia repar
Experimental group
Treatment:
Procedure: ventral hernia repair
enhanced view totally extraperitoneal laparoscopic ventral hernia repair
Experimental group
Treatment:
Procedure: ventral hernia repair
open sublay ventral hernia repair
Experimental group
Treatment:
Procedure: ventral hernia repair

Trial contacts and locations

1

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Central trial contact

mohamed badr; samir ammar, MD

Data sourced from clinicaltrials.gov

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