Comparison Open Lichtenstein Repair and Totally Extraperitoneal Herniorrhaphy

• Sponsor: Uşak University (Other)
• Overall Status: Completed
• CT.gov ID: NCT03820570
• Collaborator: (none)
• Enrollment: 200
• Arm: 1
• Actual Duration (Months): 71

Study Details

Study Description

Brief Summary

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

Condition or Disease	Intervention/Treatment	Phase
Inguinal Hernia	Procedure: hernia repair	N/A

Detailed Description

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

Study Design

• Study Type: Interventional
• Actual Enrollment: 200 participants
• Allocation: N/A
• Intervention Model: Single Group Assignment
• Masking: None (Open Label)
• Primary Purpose: Treatment
• Official Title: Comparison of Early and Long Term Outcomes of Open Lichtenstein Repair and Totally Extraperitoneal Herniorrhaphy for Primary Inguinal Hernias
• Actual Study Start Date: Jan 1, 2012
• Actual Primary Completion Date: Jan 1, 2015
• Actual Study Completion Date: Dec 1, 2017

Arms and Interventions

Arm	Intervention/Treatment
Experimental: lichtenstein hernia repair	Procedure: hernia repair; inguinal hernia repair

Outcome Measures

Primary Outcome Measures

1. recurrence [3 years]

   hernia recurrence

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Inclusion Criteria:

• inguinal hernia

Exclusion Criteria:

• recurrent hernia

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

• Uşak University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Uşak University
• ClinicalTrials.gov Identifier: NCT03820570
• Other Study ID Numbers: TEPP
• First Posted: Jan 29, 2019
• Last Update Posted: Jan 29, 2019
• Last Verified: Jan 1, 2019

• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Additional relevant MeSH terms: Hernia; Hernia, Inguinal

Study Results

No Results Posted as of Jan 29, 2019