Comparing sutures for abdominal surgery wound healing
Abdominal Wall Dehiscence After Laparotomy Closure in Abdominal Surgery: a Retrospective Observational Study on the Influence of the Suture Used
This study looks at whether using Stratafix Symmetric sutures during abdominal surgery helps prevent complications like wound reopening and hernias compared to other types of sutures.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 1900 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz Academic / other |
| Locations | 4 sites (Collado-Villalba, Madrid and 3 other locations) |
| Trial ID | NCT06501508 on ClinicalTrials.gov |
What this trial studies
This observational study examines the incidence of abdominal wall dehiscence and incisional hernia in patients who underwent abdominal surgery, focusing on the use of Stratafix Symmetric sutures compared to other suture types. It analyzes various risk factors that may influence the occurrence of fascial dehiscence. The study utilizes retrospective data to assess outcomes such as mortality and hospital stay related to abdominal wall dehiscence over a 12-month follow-up period. Statistical techniques will be employed to evaluate the data collected from patient records.
Who should consider this trial
Good fit: Ideal candidates are adults over 18 who have undergone abdominal surgery with an incision.
Not a fit: Patients who are pregnant, have a history of ventral abdominal hernia surgery, or used mesh for fascial closure will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved surgical techniques and reduced complications related to abdominal surgery.
How similar studies have performed: Other studies have explored similar suture types, but the specific focus on Stratafix Symmetric in this context may provide novel insights.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age over 18 years, abdominal incision or laparoscopy with extraction site incision Exclusion Criteria: * Pregnancy, use of mesh for fascial closure in primary surgery, history of ventral abdominal hernia surgery
Where this trial is running
Collado-Villalba, Madrid and 3 other locations
- Hospital universitario General de Villalba — Collado-Villalba, Madrid, Spain (Recruiting)
- Hospital Universitario Infanta Elena — Valdemoro, Madrid, Spain (Recruiting)
- Hospital Universitario Fundación Jiménez Díaz — Madrid, Spain (Recruiting)
- Hospital Universitario Rey Juan Carlos — Madrid, Spain (Recruiting)
Study contacts
- Principal investigator: Hector Gauadalajara Labajo, PHD — Quironsalud
- Study coordinator: Hector Gauadalajara Labajo, PHD
- Email: h.guadalajara@quironsalud.es
- Phone: 0034649429243
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.