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Not yet recruitingNCT07910240Updated Nov 2, 2026

Bassini Repair Versus Desarda Technique in Urgent Complicated Inguinal Hernia Repair

An interventional study of Bassini Inguinal Herniorrhaphy and Desarda Inguinal Hernia Repair in Inguinal Hernia, Incarcerated Inguinal Hernia and Strangulated Inguinal Hernia, sponsored by Assiut University. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-11-02.

Sponsored by Assiut University · Not applicable, Interventional, and Treatment

Updated Nov 2, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
70
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Inguinal hernias occur when abdominal contents, such as intestine or fat, protrude through a weakness in the lower abdominal wall. While most hernia repairs are scheduled electively, some hernias present as urgent emergencies due to incarceration (the contents become trapped) or strangulation (the blood supply to the trapped tissue is cut off). In emergency operations, synthetic mesh placement may be avoided due to the increased risk of surgical site infections, tissue swelling, or bowel contamination. In such settings, surgeons rely on tissue-based (mesh-free) repairs. The conventional Bassini repair is a standard non-mesh technique, but it can be associated with higher hernia recurrence rates. The Desarda technique is a physiological, mesh-free repair that uses an undetached strip of the patient's own external oblique aponeurosis (tendinous muscle tissue) to reinforce the weakened inguinal floor without tension.

The main objective of this study is to compare the surgical outcomes of conventional Bassini repair alone versus Bassini repair combined with the Desarda technique in adult patients undergoing emergency surgery for urgent, complicated inguinal hernias.

This prospective randomized controlled trial is conducted at the Department of General Surgery, Assiut University Hospital. A total of 70 eligible participants presenting with acutely complicated inguinal hernias will be randomly assigned to one of two equal groups:

  • Group A (Bassini Repair): Patients undergo standard open emergency tissue herniorrhaphy alone.
  • Group B (Desarda Repair): Patients undergo emergency herniorrhaphy combined with the Desarda aponeurotic reinforcement technique.

Participants are monitored during their hospital stay and will attend structured outpatient follow-up visits up to 12 months postoperatively. The primary outcome evaluated is the rate of hernia recurrence. Secondary outcomes include surgical site infections, seroma and hematoma formation, postoperative pain scores (using the Visual Analogue Scale), duration of operative procedure, hospital stay length, and time required to resume normal activities and return to work.

02

Conditions studied

  • Inguinal Hernia
  • Incarcerated Inguinal Hernia
  • Strangulated Inguinal Hernia

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Keywords

  • Bassini repair
  • Desarda technique
  • Emergency hernia repair
  • Complicated inguinal hernia
  • Tissue-based repair
  • Non-mesh repair
  • Herniorrhaphy
03

In context

Hernia, Inguinal

567 studies on the registry are indexed under Hernia, Inguinal; 80 are open to participants now.

This study's planned enrollment of 70 is below the median of 90 across 420 interventional studies indexed under Hernia, Inguinal.

Browse Hernia, Inguinal studies →

Lead sponsor

Assiut University is the lead sponsor of 5,068 studies on the registry; 2,179 are open to participants now.

Of its 14 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients aged 18 years and older
  • Urgent presentation of complicated inguinal hernia (incarcerated or strangulated)
  • American Society of Anesthesiologists (ASA) Physical Status Classification I, II, or III
  • Provision of signed written informed consent

Exclusion criteria

Exclusion Criteria:

  • Age under 18 years
  • Elective (non-urgent) inguinal hernia presentations
  • Recurrent inguinal hernia (history of prior ipsilateral groin or inguinal surgery)
  • Documented coagulopathy or long-term anticoagulation therapy that cannot be reversed preoperatively
  • American Society of Anesthesiologists (ASA) Physical Status Classification IV or V
  • Refusal to provide written informed consent
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
70 participants (estimated)

Study arms

  • Active comparator
    Group A: Bassini Repair (Herniorrhaphy Alone)

    Patients undergo open emergency inguinal hernia repair via a transverse groin incision. The hernia sac is dissected, contents reduced (with bowel resection and primary anastomosis performed if non-viable), and high ligation performed at the deep ring using a 2-0 polypropylene suture. Posterior inguinal canal wall repair is performed using the Bassini technique: interrupted 0-polypropylene sutures approximate the conjoint tendon (inguinal falx) to the shelving edge of the inguinal ligament from the pubic tubercle to the deep inguinal ring without prosthetic mesh. The external oblique aponeurosis is closed over the cord using 2-0 polyglactin.

    Procedure: Bassini Inguinal Herniorrhaphy

  • Experimental
    Group B: Herniorrhaphy Combined with Desarda Technique

    Patients undergo open emergency repair with identical initial access, sac reduction, and high ligation as Group A. Following high ligation, a 2-3 cm wide by 7-9 cm long strip is fashioned from the lower leaf of the external oblique aponeurosis (EOA), left undetached laterally near the deep ring. The medial free end is sutured to the conjoint tendon at the pubic tubercle with interrupted 0-polypropylene sutures, and the inferior border is sutured to the shelving edge of the inguinal ligament up to the deep ring. The upper leaf of the EOA is sutured to the superior edge of the strip with 2-0 polyglactin, providing a physiological, tension-free posterior wall repair without prosthetic mesh.

    Procedure: Desarda Inguinal Hernia Repair

Interventions

  • ProcedureBassini Inguinal Herniorrhaphy

    Standard open tissue-based repair performed without prosthetic mesh. Through a transverse groin incision, the hernia sac is dissected, contents reduced (non-viable bowel resected with primary anastomosis), and high transfixion ligation completed at the deep ring with a 2-0 polypropylene suture. Posterior inguinal canal wall reconstruction is achieved by placing interrupted 0-polypropylene sutures approximating the conjoint tendon (inguinal falx) to the shelving edge of the inguinal ligament from the pubic tubercle to the deep ring. The external oblique aponeurosis is then closed over the spermatic cord using 2-0 polyglactin.

  • ProcedureDesarda Inguinal Hernia Repair

    Open tissue-based repair reinforcing the posterior inguinal canal wall using an autologous aponeurotic strip without prosthetic mesh. Following standard sac dissection, content reduction, and high ligation, a rectangular strip measuring 2-3 cm wide and 7-9 cm long is created from the lower leaf of the external oblique aponeurosis (EOA), remaining attached laterally near the deep ring. The medial free end is sutured to the conjoint tendon at the pubic tubercle, and the inferior border is sutured to the inguinal ligament using interrupted 0-polypropylene sutures. The upper leaf of the EOA is then sutured to the superior margin of the strip with 2-0 polyglactin.

06

What researchers measure

Primary outcomes

  1. Incidence of Inguinal Hernia Recurrence

    Defined as the presence of any clinically detectable protrusion or bulge in the ipsilateral groin or inguinal region on physical examination, confirmed objectively by high-resolution inguinal ultrasonography.

    Time frame: 12 months postoperatively

07

Study locations

No study locations are listed for this record.

08

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Nov 2, 2026
Show all 1 update
  1. Nov 2, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07910240
Lead sponsor
Assiut University
Responsible party
Hossam Mamdouh Mohamed Abdellatif (Resident, Assiut University) — Principal investigator
First posted
Nov 2, 2026
Start date
Nov 2026 (estimated)
Primary completion
Nov 2027 (estimated)
Completion
Dec 2027 (estimated)
Last update
Nov 2, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

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