Viewing Study NCT00905320


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Study NCT ID: NCT00905320
Status: COMPLETED
Last Update Posted: 2021-04-20
First Post: 2009-05-18
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Hernia Repair With or Without Sutures
Sponsor: Indiana University
Organization:

Study Overview

Official Title: Sutures or No Sutures (SONS)
Status: COMPLETED
Status Verified Date: 2021-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: SONS
Brief Summary: This is a randomized study between two accepted techniques of mesh fixation for laparoscopic hernia repair.
Detailed Description: This is a randomized study in which subjects will undergo one or two currently accepted techniques of mesh fixation during laparoscopic ventral hernia repair. Subject will undergo mesh fixation with either trans-abdominal sutures and metallic tacks or metallic tacks only.

Pain will be assessed through week 12, and hernia recurrence will be assessed for 2 years after surgery. Subjects will complete pain questionnaires at baseline, each day during hospital stay, and at follow-up visits at 2, 6, and 12 weeks after discharge. Quality of life questionnaires will be completed at baseline, at discharge from hospital, and during follow-up visits at 2, 6, and 12 weeks after discharge.

Study Oversight

Has Oversight DMC: True
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: