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Desarda Repair Compared to Lichtenstein Repair for the Treatment of Inguinal Hernias

Mesh Free Desarda Repair Compared With Lichtenstein Repair for the Treatment of Primary Inguinal Hernias

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04850131
Enrollment
82
Registered
2021-04-20
Start date
2019-05-01
Completion date
2021-03-30
Last updated
2021-04-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Pain, Recurrence, Wound Complication

Keywords

Desarda Repair, Comparison, Lichtenstein Repair, Randomized Controlled Trial

Brief summary

The Lichtenstein technique for hernia repair is safe and simple, but the underlying mesh prosthesis has its setbacks, as it acts as a mechanical barrier5. The mesh does not provide mobile and the physiologically dynamic posterior wall. The most dangerous complication associated with the mesh prosthesis is its migration from the abdominal cavity's primary implantation site. The relatively knew technique developed by Dr. Desarda does not utilize the synthetic mesh rather it uses a strip of external oblique aponeurosis to strengthen the posterior wall. Our study has compared the two methods regarding various aspects.

Interventions

PROCEDUREDesarda repair

Desarda is a new tissue-based technique developed from applying the externally oblique muscle aponeurosis in the form of an undetached strip making the posterior wall in the inguinal canal stiffer. This paper focuses on analyzing comparisons between mesh-free Desarda repair and the Lichtenstein technique for the treatment of hernia inguinalis

Sponsors

Benazir Bhutto Hospital, Rawalpindi
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Intervention model description

A total of 82 patients with inguinal hernias were selected randomly to participate in this study. They were subjected to either Lichtenstein hernioplasty or Desarda herniorrhaphy. A follow-up was conducted to analyze the hospital stay, return to work, recurrence rate, chronic pain, postoperative complications, and cost-effectiveness.

Eligibility

Sex/Gender
ALL
Age
20 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

1. Patients of age between 20 to 70years 2. A primary inguinal hernia 3. Consented to participate in the research.

Exclusion criteria

1. Age below 20, 2. Recurrent and pantaloons hernia 3. Patients who did not give the informed consent 4. Patients who lose the follow-up

Design outcomes

Primary

MeasureTime frameDescription
Postoperative pain24 hours after the surgeryMeasured on Visual analogue scale (VAS) where 0 meaning no pain and 10 means worst pain
RecurrenceWithin 01 year of the primary surgeryDescribed as reappearance of the inguinal hernia on the operated side

Secondary

MeasureTime frameDescription
Wound complicationComplications occuring within 30 days after the surgeryDescribed as number of patients developing the wound complications like seroma , hematoma formation and surgical site infection.

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026