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NCT07340918
Comparison of Small-bite Versus Conventional Midline Fascial Closure in Abdominal Surgeries
trial in Incisional Hernia/Prevention and Control in 217 participants. Completed in 31 July 2024.
31 July 2024
Quick facts
| Lead sponsor | Muğla Sıtkı Koçman University |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 217 |
| Start date | 1 May 2021 |
| Primary completion | 31 July 2024 |
| Estimated completion | 31 July 2024 |
| Sites | 1 location across Turkey (Türkiye) |
Conditions studied
- Incisional Hernia/Prevention and Control — all drugs for Incisional Hernia/Prevention and Control →
- Surgical Site Infection (SSI) — all drugs for Surgical Site Infection (SSI) →
Sponsor
Muğla Sıtkı Koçman University
Who can join
18 and older, any sex, with Incisional Hernia/Prevention and Control or Surgical Site Infection (SSI). Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This study investigates how different incision and fascial closure (suture) techniques used in abdominal surgery are associated with the development of incisional hernia, a common long-term complication after laparotomy. Incisional hernia can cause pain, impaired quality of life, and may require additional surgery, making its prevention clinically important. Adult patients undergoing midline abdominal surgery were followed prospectively. During surgery, detailed information about the incision and closure technique was recorded, including the type of fascial closure (small-bite versus conventional technique), incision length, suture length, and the suture-to-wound length ratio. Patient-related factors such as age, body mass index, comorbidities, and preoperative laboratory values were also collected. After surgery, patients were monitored for early wound complications, such as surgical site infection or wound dehiscence, and were followed for up to 12 months to assess whether an incisional hernia developed. Hernia diagnosis was based on clinical examination and ultrasonographic evaluation. The main goal of the study is to identify which technical and patient-related factors are independently associated with the risk of incisional hernia. In particular, the study evaluates whether the small-bite fascial closure technique, which uses smaller and more closely spaced stitches, is associated with a lower risk of hernia formation and wound complications compared with conventional closure methods. Secondary objectives include assessing factors related to early postoperative wound complications and length of hospital stay. By integrating surgical technique details with patient characteristics and postoperative outcomes, this study aims to improve understanding of modifiable risk factors for incisional hernia. The results may help surgeons choose closure techniques more effectively and improve postoperative outcomes for patients undergoing abdominal surgery.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Small-bite versus conventional midline fascial closure in abdominal surgery: a prospective observational cohort study.
Tanrıverdi E, Şahin S, Yazkan C, Dere Ö, et al · · 2026 · PMID 41580707 · DOI 10.1186/s12893-026-03530-x
Verify or expand the search:
- PubMed search for NCT07340918
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Incisional Hernia/Prevention and Control
Currently open trials in the same condition.
- NCT07154277 — Small Bites Vs Large Bites Abdominal Midline Incisional Closure · Phase 2, PHASE3 · active not recruiting
Other Muğla Sıtkı Koçman University trials
Trials by the same sponsor.
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- NCT06704399 — Psychoeducation Based on Acceptance and Commitment Therapy · NA · not yet recruiting
- NCT07183956 — Comparison of the Silverman-Andersen Score and the Downes Score · not yet recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT07340918 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Muğla Sıtkı Koçman University
- Last refreshed: 15 January 2026
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07340918.
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