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This is a randomized study between two accepted techniques of mesh fixation for laparoscopic hernia repair.
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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Metallic Fasteners and Sutures | Active Comparator | Laparoscopic ventral hernia repair with mesh fixation using both metallic fasteners and transabdominal sutures |
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| Metallic Fasteners Alone | Experimental | Laparoscopic ventral hernia repair with mesh fixation using metallic fasteners alone |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Metallic Fasteners and Sutures | Procedure | Subjects will undergo hernia repair with mesh fixation. Fixation involves using metallic fasteners and sutures. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Post-op Pain | Short-Form McGill Pain Questionnaire (SFMP) | 12 Weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Hernia recurrence | CT Scan | 2 Years |
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Inclusion Criteria:
Demographics:
Pre-Operative Findings:
Exclusion Criteria:
Pre-Operative History:
Severe medical co-morbidities that prevent safe performance of laparoscopic surgery including coronary artery disease, obstructive pulmonary disease, etc.
History of the following:
Allergy to products used in hernia repair including surgical mesh
Any abdominal ventral incisional hernia previously repaired with permanent synthetic mesh placed inside the peritoneal cavity
Loss of abdominal domain (i.e. majority of abdominal organs lie outside confines of the abdominal musculature and fascia)
Presence of simultaneous intra-abdominal infection
Simultaneous presence of a bowel obstruction
History of suspected or known addiction to or abuse of illicit drug(s), prescription medicine(s), or alcohol within the past 2 years.
Uncontrolled anxiety, schizophrenia, or other psychiatric disorder that, in the opinion of the Investigator, may interfere with study assessments or compliance.
Intra-operative Findings:
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| Name | Affiliation | Role |
|---|---|---|
| Don Selzer, MD | Indiana University Department of Surgery | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Indiana University | Indianapolis | Indiana | 46202 | United States |
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| ID | Term |
|---|---|
| D006547 | Hernia |
| ID | Term |
|---|---|
| D020763 | Pathological Conditions, Anatomical |
| D013568 | Pathological Conditions, Signs and Symptoms |
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| ID | Term |
|---|---|
| D013537 | Sutures |
| ID | Term |
|---|---|
| D053831 | Surgical Fixation Devices |
| D013523 | Surgical Equipment |
| D004864 | Equipment and Supplies |
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| Metallic Fasteners Alone | Procedure | Subjects will undergo hernia repair with mesh fixation. Fixation involves using metallic fasteners alone. |
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