CClinicalTrials.gg
CompletedNCT06856304Updated Mar 4, 2025

Percutaneous Internal Ring Suturing Versus Conventional Laparoscopic Repair of Congenital Inguinal Hernia

An interventional study of laparoscopic disconnection of the hernia sac and Percutaneous internal ring suturing in Pediatrics and Inguinal Hernia Repair, sponsored by Alexandria University. Completed at 1 site in Egypt. Open to male participants aged 6 Months to 5 Years. Per ClinicalTrials.gov, last updated 2025-03-04.

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

From the registry’s dates

  • Registered 2 years 9 months after the study started (first participant enrolled May 2022, registered Feb 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
109
Allocation
Randomized
Ages
6 Months to 5 Years
Sex
Male
01

Study summary

Background:comparison between percutaneous internal ring suturing vs Conventional Laparoscopic Repair of Congenital Inguinal Hernia in male patients. Methods : this is a prospective randomized study including 109 male patients with 120 CIHs Patients were randomly categorized into two groups. Group A were subjected to laparoscopic disconnection of the hernia sac and narrowing of the internal ring (IR). Group B underwent PIRS. The intended primary outcome was recurrence within 1 year, besides comparing the two techniques regarding operative time, efficacy, safety, cosmetic outcome, and postoperative complications.

Read the detailed description

Introduction Since the 1990s laparoscopy has gained popularity in the management of Congenital inguinal hernia (CIH). Several laparoscopic techniques have been described, including laparoscopic disconnection of the hernial sac with narrowing of the internal ring (IIR) which was described to mimic the open technique, and the extraperitoneal approach involves using various types of needles under laparoscopic guidance to percutaneously secure a suture circumferentially around the internal ring, thus obliterating the sac opening. This study compared the short-term outcome of percutaneous internal ring suturing (PIRS) versus laparoscopic disconnection of the hernial sac with narrowing of the internal ring in children.

Materials and Methods: This study included 109 male patients with 120 CIHs during the period from May 2022 to May 2024. Patients were randomly categorized into two groups. Group A were subjected to laparoscopic disconnection of the hernia sac and narrowing of the internal ring (IR). Group B underwent PIRS. The intended primary outcome was recurrence within 1 year, besides comparing the two techniques regarding operative time, efficacy, safety, cosmetic outcome, and postoperative complications.

02

Conditions studied

  • Pediatrics
  • Inguinal Hernia Repair

Keywords

  • Laparoscopy
  • inguinal hernia
  • PIRS
  • sac disconnection
  • Narrowing of the internal ring
03

In context

Hernia

1,096 studies on the registry are indexed under Hernia; 132 are open to participants now.

This study's enrollment of 109 is above the median of 80 across 739 interventional studies indexed under Hernia.

Browse Hernia studies →

Lead sponsor

Alexandria University is the lead sponsor of 569 studies on the registry; 125 are open to participants now.

Of its 12 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
6 Months to 5 Years
Sexes eligible
Male
Accepts healthy volunteers
No

Inclusion criteria

  • male patients
  • age of 6 month to 5years
  • reduciable congenital inguinal hernia either unilateral or bilateral.

Exclusion criteria

Exclusion Criteria:

  • incarcerated CIH
  • recurrent CIH
  • patients with undescended testis,
  • patients with hydrocele,
  • patients with chronic comorbidity such as congenital heart disease and severe chest troubles
05

Study design

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

Study arms

  • Experimental
    Group A

    laparoscopic disconnection of the hernia sac and narrowing of the internal ring

    Procedure: laparoscopic disconnection of the hernia sac

  • Experimental
    Group B

    Percautaneous internal ring suturing

    Procedure: Percutaneous internal ring suturing

Interventions

  • Procedurelaparoscopic disconnection of the hernia sac

    disconnection of the hernial sac at the level of the internal ring using hook diathermy with sweeping the vas and the vessels away till completely separating them from the edges of the sac, then narrowing of the internal ring by appling a vicryl 3/0 suture between the ilipubic tract and the transverse arch of the transversus abdominus muscle

  • ProcedurePercutaneous internal ring suturing

    A single umbilical trocar was placed through a supraumbilical incision, and then the surgeon stood on the same side of the hernia. To choose the location for the needle puncture, the position of the IIR was assessed by pressing the inguinal region from the outside with the tip of a forceps. Under laparoscopic-guided vision, the previously prepared 18-gauge injection needle threaded with the monofilament suture was introduced into the abdominal wall through a skin puncture at the lateral edge of the internal ring. With the movements of the tip of the needle, the thread passed under the peritoneum, over the lateral half of the IIR. The thread was pushed through the barrel of the needle into the abdominal cavity and eventually made a loop. The needle was pulled out, leaving the loop of the thread inside the abdomen by hanging the loop on the endoscope this prevented the extraction of the loop with the needle and thus prevented repeating this step. Next, the thread loop was pulled out of t

06

What researchers measure

Primary outcomes

  1. operative time

    time of the procedure estimated after trocars insertion and Inflation of the abdomen till deflation of the abdomen

    Time frame: the time estimated during the operation

  2. intraoperative safety

    injury of the vas deffernce , spermatic vessels , bleeding

    Time frame: the time estimated during the operation

  3. Recurrence of the inguinal hernia

    postoperative swelling in the inguinal region with gurgling sensation

    Time frame: 1 year

Secondary outcomes

  1. cosmesis

    postoperative scar

    Time frame: 1 year

07

Study locations

1 site
  • Faculty of Medicine
    Alexandria, 12345, Egypt
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 4, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06856304
Lead sponsor
Alexandria University
Responsible party
Sponsor
First posted
Mar 4, 2025
Start date
May 1, 2022
Primary completion
May 30, 2023
Completion
May 30, 2024
Last update
Mar 4, 2025

Study contacts

Mohamed Abouheba, Assistant Professor
study director · University of Alexandria

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2022. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion