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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05420376
Other study ID # 569874
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 16, 2022
Est. completion date June 16, 2023

Study information

Verified date July 2022
Source Istanbul Training and Research Hospital
Contact Erol Aydin, MD
Phone +905322546001
Email erolay@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Recruiting
Enrollment 80
Est. completion date June 16, 2023
Est. primary completion date May 16, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Clinical or/and radiological diagnosed primary inguinal hernia - TEP or TAPP surgical methods Exclusion Criteria: - Recurrent hernias - Patients with previous groin operations on same side - Pregnant women - Patients who did not accept to participate in the study - ASA score of 3 or higher,

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Split Mesh
TEP repair of inguinal hernias using either split or whole mesh

Locations

Country Name City State
Turkey Istanbul Training and Research Hospital Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Istanbul Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Carolinas Comfort Scale values Differences in postoperative pain and quality of life(Carolinas Comfort Scale at first month) in patients who use whole meshes and those who use split meshes. 6 month
Primary Recurrence rates Differences in recurrence rates in patients who use whole meshes and those who use split meshes. 6 month
Secondary Recurrence rates Difference in recurrence rates at 6 months in patients who use whole meshes and those who use split meshes. 6 month
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