Needlescopic Versus Traditional Laparoscopic Inguinal Hernia Repair in Pediatrics

November 26, 2024 updated by: Abdelaziz Ali Abdelaziz, Sohag University

Needlescopic Versus Traditional Laparoscopic Inguinal Hernia Repair in Pediatrics (A Prospective Comparative Study)

The aim of the study is to evaluate the results of Needlescopic inguinal hernia repair in comparison with traditional laparoscopic repair in children as regard operative time, cosmetic appearance, recurrence and other complications.

Study Overview

Detailed Description

Patients and methods:

  • Place of the study: The study will be held in Department of Pediatric surgery in Sohag University Hospital.
  • Type of the study: Prospective comparative Cohort study.
  • Duration of the study: The study will last for 6 to 9 months starting from the date of acceptance of the protocol.
  • Ethical considerations: The study will be carried out after approval by scientific and ethical committees of Sohag faculty of medicine.
  • Method of the study:

Preoperative assessment:

  1. Demographic data: e.g. name, age, sex …. etc.
  2. History: e.g. complaint, present history and past surgical and medical history…etc.
  3. General and local examination: e.g. laterality, associated anomalies …. etc.
  4. Investigations:

Routine labs. Imaging: to confirm diagnosis in the affected side, to evaluate contralateral side, bilateral testicular volume as volumetric stander to evaluate testicular atrophy postoperative and other anomalies.

Operative technique:

Operative steps:

A. Traditional laparoscopic repair.

  • STEPS:

    1. A 5mm port for the camera is introduced at umbilicus by open technique.
    2. Using triangulation rule to introduce two working ports.
    3. The abdomen is insufflated with carbon dioxide to 6-8 mmHg pressure in patients under 1 year of age and to 8-10 mmHg in older children.
    4. Diathermize the neck of the hernia sac with a diathermy hook.
    5. A 10-15 cm absorbable suture is passed into the peritoneal cavity through the abdominal wall next to the lateral port under vision.
    6. The purse-string stitch commences at the 2 o'clock position of the internal hernia opening.
    7. ensure that a "complete ring" of peritoneum has been included in the purse-string stitch without significant gaps.
    8. The purse-string suture is tied tightly using intracorporeally knot tying.

      B. Needlescopic Internal Ring Suturing.

  • EQUIPMENT/SUTURE:

    1. One 5-mm trocar and 5-mm lens 30° or 0° telescope.
    2. Epidural needle.
    3. Non absorbable suture.
    4. Fascial closure instrument.
  • STEPS:

    1. A 5mm port for the camera is introduced at umbilicus by open technique.
    2. The abdomen is insufflated with carbon dioxide to 6-8 mmHg pressure in patients under 1 year of age and to 8-10 mmHg in older children.
    3. The suture is introduced through the barrel of the epidural needle.
    4. Maintaining both ends of the preloaded suture extra peritoneal, the needle is advanced under the peritoneum around lateral half of the internal ring.
    5. The peritoneum is entered and the suture advanced into the abdominal cavity, creating a loop.
    6. Fascial closure instrument is introduced directly through anterior abdominal wall to help to maintain suture loop.
    7. The needle is removed, leaving the loop in place.
    8. The needle is entered again through the same skin puncture site around the medial half of the ring and enter the peritoneum, leaving a small space above the vas deferens and testicular vessels to avoid injury.
    9. The loop of suture is introduced into the hollow of the needle again and advance the suture into the first loop by the help of fascial closure.
    10. Withdraw the needle.
    11. Catch the suture end in the loop and withdraw them together then the suture is tied extra corporeally.

Patient outcomes:

Patients assessment and follow up:

  1. Primary outcome measures:

    Operative time. Intraoperative complication. Rate of conversion to open surgery.

  2. Secondary outcome measures:

1 and 3 months after the surgery to asses:

  1. Cosmetic appearance: according to (The Scar Cosmesis Assessment and Rating "SCAR" Scale) [7].
  2. Recurrence.
  3. Hydrocele.
  4. Testicular atrophy (postoperative imaging: > 50% loss of testicular volume or < 25% of volume of contralateral testis) [8].

Study Type

Interventional

Enrollment (Estimated)

20

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

  • Name: Ahmed M Abd El-Moniem, Professor
  • Phone Number: 00201005768450

Study Locations

      • Sohag, Egypt
        • Recruiting
        • Sohag University Hospitals
        • Contact:
        • Contact:
          • Ahmed M Abd El-Moniem, Professor
          • Phone Number: 00201005768450

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Include patients presented with inguinal hernia with age < 18 years.

Exclusion Criteria:

  1. Age above 18 years.
  2. Complicated inguinal hernia (e.g. irreducibility, obstruction and strangulation).
  3. Pervious lower abdominal surgeries.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Needlescopic inguinal hernia repair
Needlescopic inguinal hernia repair
Active Comparator: Traditional laparoscopic inguinal hernia repair
traditional laparoscopic repair

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Operative time
Time Frame: during operation
Operative time from start of incision making till end of operation and closure of incisions
during operation
Intraoperative complications
Time Frame: during operation
as injury to inferior epigastric vessels, vas deferens and major pelvic vessels
during operation
Rate of conversion to open surgery.
Time Frame: during operation
rate of conversion from laparoscopic surgery to open surgery.
during operation

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Cosmetic appearance
Time Frame: 1 and 3 months after the surgery
according to (The Scar Cosmesis Assessment and Rating "SCAR" Scale)
1 and 3 months after the surgery
Recurrence
Time Frame: 1 and 3 months after the surgery
recurrence of inguinal hernia diagnosed clinically and/or by ultrasound
1 and 3 months after the surgery
Hydrocele
Time Frame: 1 and 3 months after the surgery
diagnosed clinically and/or by ultrasound
1 and 3 months after the surgery
Testicular atrophy
Time Frame: 1 and 3 months after the surgery
diagnosed clinically and/or by ultrasound (postoperative imaging: > 50% loss of testicular volume or < 25% of volume of contralateral testis).
1 and 3 months after the surgery

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

  • 1. Cóbar, J. P., & Nichol, P. F. (2023). Introduction of pediatric laparoscopic inguinal hernia repair in Guatemala. BMC Surgery, 23(1). 2. Chang, S., Chen, J. Y., Hsu, C., Chuang, F., & Yang, S. S. D. (2015). The incidence of inguinal hernia and associated risk factors of incarceration in pediatric inguinal hernia: a nation-wide longitudinal population-based study. Hernia, 20(4), 559-563. 3. Elhosary, M. A., Elbatarny, A. M., Arafa, M., Mahmoud, S. M., Ismail, K. A., et al. (2023). Needlescopic primary paediatric inguinal hernia repair by hernia sac disconnection and peritoneal closure. Journal of Pakistan Medical Association, 73(4), S61-S66. 4. Maat, S. C., Dreuning, K. M. A., Nordkamp, S., Van Gemert, W., Twisk, J. W. R., et al. (2021). Comparison of intra- and extra-corporeal laparoscopic hernia repair in children: A systematic review and pooled data-analysis. Journal of Pediatric Surgery, 56(9), 1647-1656. 5. Hajong, R., Newme, K., & Moirangthem, T. (2022). A case control study of needlescopic herniotomy versus open herniotomy in children. Journal of Family Medicine and Primary Care, 11(7), 3633. 6. Shalaby, R., Negm, M., Elsawaf, M., Elsaied, A., Shehata, S., et al. (2021). Needlescopic disconnection and peritoneal closure for Pediatric inguinal hernia repair: a Novel technique. Surgical Laparoscopy Endoscopy & Percutaneous Techniques, 32(2), 272-278. 7. Kantor J, et al. Reliability and photographic equivalency of the SCAR Cosmesis assessment and rating (SCAR) scale, an outcome measure for postoperative scars. JAMA Dermatol. 2017;153(1):55-60 8. Ein, S.H. ∙ Nasr, A. ∙ Wales, P.W. ... Testicular atrophy after attempted pediatric orchidopexy for true undescended testis J Pediatr Surg. 2014; 49:317-322.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 1, 2024

Primary Completion (Estimated)

May 1, 2025

Study Completion (Estimated)

August 1, 2025

Study Registration Dates

First Submitted

October 24, 2024

First Submitted That Met QC Criteria

October 25, 2024

First Posted (Actual)

October 28, 2024

Study Record Updates

Last Update Posted (Estimated)

November 27, 2024

Last Update Submitted That Met QC Criteria

November 26, 2024

Last Verified

November 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • Soh-Med-15-10-4MS

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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