NCT05655988 is a NA clinical trial of inguinal ultrasonography in Inguinal Hernia, sponsored by Fatih Sultan Mehmet Training and Research Hospital.

Who is sponsoring NCT05655988?

NCT05655988 is sponsored by Fatih Sultan Mehmet Training and Research Hospital.

What drugs are being tested in NCT05655988?

Interventions in NCT05655988: inguinal ultrasonography.

What condition does NCT05655988 study?

NCT05655988 studies Inguinal Hernia.

Is NCT05655988 still recruiting?

NCT05655988 is currently status unknown. Last updated 19 December 2022.

Last reviewed 2022-12-19 · How we verify

NCT05655988

Name: Drug Landscape Pharmaceutical Database
Creator: Drug Landscape
Published: 2026-01-01
License: https://creativecommons.org/licenses/by/4.0/

MESH MIGRATION IN TOTAL EXTRAPERITONEAL INGUINAL HERNI REPAIR

Status unknown NA Last updated 19 December 2022

What this trial tests

NA trial testing inguinal ultrasonography in Inguinal Hernia in 72 participants. Status unknown.

Timeline

15 December 2022

Primary endpoint
15 December 2023

15 January 2024

Quick facts

Lead sponsor	Fatih Sultan Mehmet Training and Research Hospital
Phase	NA
Status	Status unknown
Study type	INTERVENTIONAL
Allocation	randomized
Design	parallel
Masking	triple
Primary purpose	treatment
Enrollment	72
Start date	15 December 2022
Primary completion	15 December 2023
Estimated completion	15 January 2024
Sites	1 location across Turkey (Türkiye)

Drugs / interventions tested

inguinal ultrasonography

Conditions studied

Inguinal Hernia — all drugs for Inguinal Hernia →

Sponsor

Fatih Sultan Mehmet Training and Research Hospital

Who can join

18 and older, any sex, with Inguinal Hernia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Inguinal henri repair is among the most common operations performed by general surgery. The use of laparoscopy in inguinal hernia repair is becoming more common day by day. Laparoscopic inguinal hernia repair is being applied with increasing frequency due to its advantages such as reducing postoperative pain, providing early return to work and increasing patient satisfaction. Due to the widespread use of laparoscopic inguinal hernia repair, the best fixation method for the patches has become an increasingly questionable subject. It is thought that fixation of the patch with staples or clips may reduce the slippage of the patch, thus reducing the risk of hernia recurrence. In addition, it has been stated that the use of these fixation materials will both increase the cost and cause acute and chronic pain after surgery. In some studies in the literature, it was determined that not detecting the patch in laparoscopic inguinal hernia repair did not increase the recurrence. There are some studies showing that failure to fix the patch causes patch slippage in unilateral laparoscopic inguinal hernia repair. In this study, it was planned to investigate the rate of displacement of the patches fixed with staples in patches that do not require fixation in laparoscopic inguinal hernia repair surgeries, compared to the ones that were not fixed, and whether they cause recurrence. At the same time, whether the staples used for patch fixation increase postoperative pain will be evaluated with VAS (visual analog scale) at the postoperative 1st day, 1st month and 6th month after the operation, compared to the group without stapler patch fixation.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other recruiting trials for Inguinal Hernia

Currently open trials in the same condition.

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NCT06915155 — Swing-Mesh™ Study (SMS). · active not recruiting
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NCT04706026 — A Pilot Study of Local Anesthesia for Inguinal Hernia Surgery in Older Adults · NA · recruiting

Other Fatih Sultan Mehmet Training and Research Hospital trials

Trials by the same sponsor.

NCT07589582 — Active Noise-Cancelling Headphones Reduce Operative Time and Improve Procedural Consistency in ACL Reconstruction l · NA · active not recruiting
NCT07523828 — Laryngeal Edema Assessment by Cuff Leak Test and Ultrasound in ICU Patients and Its Relationship With Weaning Success · not yet recruiting
NCT07487038 — The Efficacy and Safety of a Single-Dose Hyaluronic Acid Injection in the Treatment of Knee Osteoarthritis · not yet recruiting
NCT07485465 — Lymphoedema Diagnosis and Treatment · not yet recruiting
NCT07451925 — Prediction of Postoperative Pain Using Venous Cannulation Pain and Preoperative Anxiety Scores · not yet recruiting

Verify against primary sources

ClinicalTrials.gov — authoritative US registry record
WHO ICTRP — international registry index
EU Clinical Trials Register
Sponsor press releases (Google)

Data sources for this page

Trial protocol + status: ClinicalTrials.gov NCT05655988 (US National Library of Medicine, public domain)
Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
Sponsor: as reported to ClinicalTrials.gov by Fatih Sultan Mehmet Training and Research Hospital
Last refreshed: 19 December 2022

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05655988.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing