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Compares treatment options for Incisional Hernia
Official title Suture Repair vs Mesh Repair for Incisional Hernia
ClinicalTrials.gov ID: NCT05599750
What this study is testing
- What it's testing
- The goal of this randomized controlled trial is to compare the difference in quality of life at one year postoperatively for patients undergoing incisional hernia repair with mesh versus suture repair using modern techniques. The main question it aims to answer are: Determine if primary suture repair is non-inferior to mesh repair for incisional hernias 2-6cm with respect to quality of life using the HerQLes summary score at one year postoperatively.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older. Healthy volunteers may be eligible.
You may be able to join if
- Adults \>18 years old.
- Anticipated hernia defect 2-6cm in width
- Non-emergent case
- CDC class I
- Patients who previously underwent primary ventral hernia repair without the use of mesh
You likely can't join if
- Emergent cases
- Patients \< 18 years old
- Patients who are pregnant
- Patients who previously underwent a prior ventral hernia repair with mesh at the site of the intended repair. Abdominal mesh in separate locations...
- Ventral hernia \ 6 cm in width
- Primary hernia
See the full eligibility criteria
- Adults \>18 years old.
- Anticipated hernia defect 2-6cm in width
- Non-emergent case
- CDC class I
- Patients who previously underwent primary ventral hernia repair without the use of mesh
- Incisional hernia
- Emergent cases
- Patients \< 18 years old
- Patients who are pregnant
- Patients who previously underwent a prior ventral hernia repair with mesh at the site of the intended repair. Abdominal mesh in separate locations would be allowed.
- Ventral hernia \ 6 cm in width
- Primary hernia
- CDC wound class II-IV
The study team makes the final eligibility decision.
Where it's taking place
- Gainesville, Florida, United States
- Chicago, Illinois, United States
- Cleveland, Ohio, United States
- Columbus, Ohio, United States
- Nashville, Tennessee, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Gainesville, Florida, United States; Chicago, Illinois, United States; Cleveland, Ohio, United States; Columbus, Ohio, United States; Nashville, Tennessee, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.