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NCT Number: NCT07318493

Antiseptic-Coated Sutures and Pancreatic Fistula Risk After Pancreatoduodenectomy

The purpose of this study is to determine if the use of antiseptic-coated sutures is better than the use of the standard sutures in preventing postoperative fistulas within 90 days after pancreatoduodenectomy.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Cleveland Clinic Akron, Akron, Ohio, United States

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About this study

This study is a randomized-controlled trial comparing the rate of post-operative pancreatic fistula (POPF) in patients undergoing pancreatoduodenectomy. This is a superiority study designed to determine whether the use of antiseptic-coated sutures (intervention arm) is superior to standard sutures (control arm) in regard to clinically significant POPF within 90 days following pancreatoduodenectomy. Patients will be randomized to receive either a pancreatoduodenectomy surgery utilizing antiseptic coated sutures or with non-coated standard sutures. The study hypothesize that the use of antiseptic-coated sutures will be associated with a reduction in the rate of POPF. Both sutures are currently available at our center and utilized in the procedure of interest.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subjects must be undergoing a scheduled pancreatoduodenectomy.
  • Age ≥18 years.
  • Subjects must have the ability to understand and the willingness to sign a written informed consent document

Exclusion criteria

  • Patients < 18 years old
  • Patients who are pregnant
  • Patients with history of previous pancreatic surgery
  • Patients who are unable to provide informed consent

Treatment and study plan

Standard (non-antiseptic coated) suture will be used.

Device

This is an operation to treat tumors and other conditions in the pancreas, small intestine, and bile ducts. It involves removing the head of the pancreas, the first part of the small intestine, the gallbladder, and the bile duct. Part of the procedure involves sutures. A suture(s) is a stitch or row of stitches holding together the edges of a wound or surgical incision

Triclosan/antiseptic -coated suture

Device

Triclosan/antiseptic -coated suture will be used. Ethicon PDSTM Plus Antibacterial Suture will be used at the layer of the pancreatojejunostomy and for the duration of the case.

Primary outcomes

  1. Comparison of the rate of postoperative pancreatic fistula

    Time frame: up to 90 days post-operative

    comparison of the rate of postoperative pancreatic fistula- Biochemical leak

  2. Comparison of the rate of postoperative pancreatic fistula

    Time frame: up to 90 days post-operative

    Comparison of the rate of postoperative pancreatic fistula-Grade B

  3. Comparison of the rate of postoperative pancreatic fistula

    Time frame: up to 90-day post operative

    Comparison of the rate of postoperative pancreatic fistula-Grade C

Secondary outcomes

  1. Improvement in Rate of clinically significant POPF

    Time frame: up to 90-days post-operative

    Improvement in Rate of clinically significant POPF (Grade B and C defined by ISGLS definition)

  2. Improvement in SSI rates between groups using CDC classification

    Time frame: up to 90-days post-operative

    Improvement in SSI rates between groups using CDC classification (superficial, deep, organ space)

  3. Hospital Length of Stay

    Time frame: up to 90-day post operative

    Duration of hospital admission, measured in days, during index presentation for pancreatoduodenectomy. This will subsequently be compared among our two cohorts (standard suture vs antiseptic suture)

  4. Length of ICU stay

    Time frame: up to 90-day post operative

    Duration of Intensive care unit admission, measured in days, during index presentation for pancreatoduodenectomy, or during convalescence from surgery. This will subsequently be compared among our two cohorts (standard suture vs antiseptic suture)

  5. Surgical Site Infection

    Time frame: up to 90-day post operative

    An infection that occurs in the part of the body where the surgery took place and includes superficial, deep, and organ space infections

  6. Surgical site occurrence

    Time frame: Up to 90 days post-operative

    Non-healing incisional wound, fascial disruption, skin or soft tissue ischemia, skin or soft tissue necrosis, wound serous or purulent drainage, stitch abscess, seroma, hematoma, wound dehiscence, and enterocutaneous fistula

  7. Surgical Site Occurrence requiring Procedural Intervention

    Time frame: up to 90 days post-operative

    Interventions to address wound healing issues or complications including wound opening or debridement, suture excision, percutaneous drainage. This includes to address superficial, deep, and organ space healing concerns

  8. Post operative pancreatic fistula interventions

    Time frame: Up to 90 days post-operative

    Postoperative interventions related to clinically relevant postoperative pancreatic leak (defined by 2016 International Study Group of Pancreatic Fistula) including percutaneous, endoscopic and surgical interventions.

Study contacts

Contact information is provided by the study sponsor or research team.

Christine Moegling, BS

CONTACT

[email protected]

216 399-4706

Sponsors and collaborators

Lead sponsor

The Cleveland Clinic

Other

Collaborators

  • Ethicon, Inc.

Registry information

Official study title

Does Antiseptic Coated Suture Reduce Pancreatic Fistula Rate After Pancreatoduodenectomy: A Randomized Controlled Trial

Acronym: Triclosan

Important dates

Study start
2026
Primary completion
2030
Study completion
2031
First posted
Jan 6, 2026
Registry last updated
Jan 21, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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