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Surgical Repair of Spigelian Hernia in a Cohort of Patients

Not Applicable
Completed
Conditions
Spigelian Hernia
Interventions
Procedure: Fixation free Spigelian hernia repair with tentacle mesh
Registration Number
NCT05379751
Lead Sponsor
University of Cagliari
Brief Summary

Repair of Spigelian hernias with a tentacle shaped implant and highlighting the results of the procedure

Detailed Description

The surgical treatment of Spigelian hernias is mainly carried out with prosthetic meshes made of biocompatible material. In prosthetic repair of abdominal protrusions, mesh fixation and overlap of the mesh are source of complications. To avoid these problems, for a fixation free repair of Spigelian hernias has been developed a tentacle shaped implant, that should also assure a broader defect overlap. This study should highlight in a cohort of patients the long-term results of fixation free repair of Spigelian hernias carried out with tentacle mesh.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
54
Inclusion Criteria
  • Patients diagnosed with Spigelian hernia
Exclusion Criteria
  • Patients not having Spigelian hernia,

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Patients diagnosed with Spigelian hernia who underwent prosthetic repair with the tentacle meshFixation free Spigelian hernia repair with tentacle meshPatients diagnosed with Spigelian hernia who underwent prosthetic repair with the tentacle mesh Freedom Octomesh VHR XS
Primary Outcome Measures
NameTimeMethod
Fixation free prosthetic repair of Spigelian hernias with tentacle meshIntraoperative

Feasibility of fixation free placement of tentacle mesh in Spigelian hernia repair

Granting a broad implant overlap in prosthetic repair of Spigelian hernias with tentacle meshbetween 6 and 84 months postop

Granting a broad overlap over the hernial defect after placement in preperitoneal sublay of tentacle mesh in Spigelian hernia repair with tentacle mesh to reduce risks of recurrence in the long term postop.

Secondary Outcome Measures
NameTimeMethod
Intra-operative featuresintraoperatively

reduction of the operative time length

Postoperative features 2between 6 and 84 months postop

Assessment of postoperative complications

Postoperative features 1between 6 and 84 months postop

Postoperative pain assessment with VAS scoring system

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