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Clinical Trials/CTRI/2018/01/011268
CTRI/2018/01/011268
Recruiting
Phase 3

Mesh fixation with penetrating fixation device versus fibrin sealant during laparoscopic repair of ventral hernia: A double blind randomised control trial double blind randomised control trial

All India Institute of Medical Sciences0 sites0 target enrollmentStarted: TBDLast updated:
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ConditionsHealth Condition 1: null- Primary ventral hernia

Overview

Phase
Phase 3
Status
Recruiting
OverviewEligibility CriteriaInvestigatorsRecords & IdentifiersSimilar Trials

Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Inclusion Criteria

  • •All consecutive patients (adult male and females \> 18 and \<65 years old) admitted for elective laparoscopic repair of primary ventral hernia.

Exclusion Criteria

  • •1\. Defect size less than 1 cm and greater than 5 cm on pre\-operative ultrasound.
  • •2\. Secondary hernias including insicional hernia or parastomal hernia
  • •3\. Non midline ventral hernia
  • •4\. Patients with ASA grade IV and V
  • •5\. Significant co\-morbidities like coronary artery disease, asthma, COPD, and previous
  • •malignancy.
  • •6\. Patients requiring other concomitant procedures.
  • •7\. Patients who do not give consent for participation in the study or patient with
  • •cognitive impairments
  • •8\. Patients on chronic analgesic use

Investigators

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