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Freedom Inguinal Hernia Repair System Study

Primary Inguinal Hernia Clinical Trial

Official title:
Freedom Inguinal Hernia Repair System Study

Clinical Trial Summary

The primary objective of this study is to evaluate patient quality-of-life (QOL) after inguinal hernia repair. "Carolinas Comfort Scale" (CCS) assessments will be held at regular intervals.

The secondary objective of the study is to follow short-term and long-term study-related complications/adverse events.

Clinical Trial Description

n/a

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01984996
Study type Interventional
Source Insightra Medical, Inc.
Contact
Status Terminated
Phase N/A
Start date December 2013
View Details
See also
  Status Clinical Trial Phase
Recruiting NCT03488342 - Rives Technique Versus Lichtenstein Repair for Primary Inguinal Hernia N/A
Terminated NCT01596049 - The Efficacy of a Self-fixating Mesh in Unilateral Open Inguinal Hernia Repair N/A
Recruiting NCT06406959 - The Effect of Preemptive Regional Anesthesia (TAP-block) on Acute and Chronic Pain After Transabdominal Preperitoneal Inguinal Hernia Repair (TAPP) N/A