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NCT03820570 Clinical Trial

Comparison Open Lichtenstein Repair and Totally Extraperitoneal Herniorrhaphy

Inguinal Hernia Clinical Trial

Official title:
Comparison of Early and Long Term Outcomes of Open Lichtenstein Repair and Totally Extraperitoneal Herniorrhaphy for Primary Inguinal Hernias

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03820570
Other study ID # TEPP
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2012
Est. completion date December 1, 2017

Study information
Verified date January 2019
Source Usak University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

comparison of early and long term results of open lichtenstein repair and totally extraperitoneal herniorrhaphy for primary inguinal hernias.

Description:

Early results such as postoperative pain, operation time and long term results such as chronic pain and recurrence will be compared.

Recruitment information / eligibility
Status Completed
Enrollment 200
Est. completion date December 1, 2017
Est. primary completion date January 1, 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- inguinal hernia

Exclusion Criteria:

- recurrent hernia

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• hernia repair
inguinal hernia repair

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Usak University

Outcome
Type Measure Description Time frame Safety issue
Primary recurrence hernia recurrence 3 years
See also
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Recruiting NCT05879770 - Is the Use of Prolene as Sufficient as the Use of Wire in Shouldice Surgery to Keep the Recurrence Rate Low After One Year?
Completed NCT05159232 - Length of Hospital Stay in Laparoscopic Transabdominal Preperitoneal Vs. Open Mesh Repair in Inguinal Hernia: A Randomised Controlled Trial N/A
Completed NCT05107986 - Laparoscopy in Complicated Groin Hernia
Active, not recruiting NCT04328597 - Portuguese Inguinal Hernia Cohort (PINE) Study
Completed NCT04033055 - Antalgic Efficacy of CycloMesh™ Soaked in Ropivacaine Hydrochloride in Uncomplicated Inguinal Hernia. N/A