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NCT05420376

Comparison of Whole Mesh and Split Mesh Use in Laparoscopic Inguinal Hernia Repair

Status unknown NA Last updated 20 July 2022
What this trial tests

NA trial testing Split Mesh in Hernia, Inguinal in 80 participants. Status unknown.

Timeline
16 June 2022
Primary endpoint
16 May 2023
16 June 2023

Quick facts

Lead sponsorIstanbul Training and Research Hospital
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment80
Start date16 June 2022
Primary completion16 May 2023
Estimated completion16 June 2023
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Istanbul Training and Research Hospital

Who can join

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

Sponsor's own description

At least 80 patients who will undergo laparoscopic inguinal hernia repair surgery will be randomized into 2 groups. For the patients in the first group, the whole mesh will be laid on the area without being fixed. The patients in the second group will be given a mesh of the same size, but partially divided horizontally and wrapped around the spermatic cord. Demographic data of patients in both groups, quality of life data(Carolinas Comfort Scale) at postoperative 1st, 7th, 30th, 3rd and 6th months, postoperative pain (VAS values), clinical seroma rate, recurrence and other complications will be monitored. When the desired number of patients and follow-up period are reached, the data in the 2 groups will be compared.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Hernia, Inguinal

Currently open trials in the same condition.

Other Istanbul Training and Research Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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/NCT05420376.

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