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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03421925
Other study ID # OkanU
Secondary ID
Status Not yet recruiting
Phase N/A
First received January 26, 2018
Last updated February 2, 2018
Start date February 1, 2018
Est. completion date February 1, 2020

Study information

Verified date February 2018
Source Okan University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Laparoscopic inguinal hernia repair techniques has been compared with the open techniques in several studies. However, no one studied about the different uses of the same type of mesh on the same surgical technique, and effects of this different use on testicular volume and blood flow. The objective of this study is to investigate the effects at 6 months of the divided and non divided mesh in laparoscopic totally extraperitoneal hernia repair technique on testicular volume and blood flow by use of Doppler Ultrasonography


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 150
Est. completion date February 1, 2020
Est. primary completion date February 1, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

Patients with unilateral inguinal hernia Male patients

Exclusion Criteria:

Patients have femoral hernia Patients have bilateral inguinal hernia Patients have recurrent inguinal hernia Female patients Patients with history of pelvic surgery Patients with history of pelvic major trauma Patients with history of pelvic radiotherapy Patients have previous scrotal trauma or surgery history Patients have heavy cardiac diseases, pulmonary diseases Patients have benign prostate hyperplasia Patients have history of incarceration of inguinal hernia

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Laparoscopic totally extraperitoneal procedure for inguinal hernia
Laparoscopic totally extraperitoneal procedure for inguinal hernia is a technique that is done by not entering the peritoneal cavity

Locations

Country Name City State
Turkey Okan University Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Okan University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Testicular volume 6 months
Secondary Testicular artery blood flow 6 months
See also
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Completed NCT05600296 - Ultrasound-guided Ilioinguinal/Iliohypogastric Nerve Block Compared to the Combined Therapy With Spermatic Cord Block Phase 1