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OpenTrials
Completed

NCT Number: NCT03419676

Use of Hemopatch as a Sealant at the Pancreaticojejunostomy After Pancreatoduodenectomy

The objective of this study is to determine the effect of the sealant patch Hemopatch, compared to current practice without any sealant, on the decrease of the postoperative pancreatic fistula on patients undergoing pancreatoduodenectomy for benign or malignant tumors or other benign process.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Mario Serradilla Martín

Zaragoza, 50008, Spain

About this study

Pancreaticoduodenectomy (PD) is the most common surgical procedure to treat pancreatic tumors in the head of the pancreas and periampullary region, as well as benign processes such as chronic pancreatitis. Recent advances in surgical techniques and perioperative treatments have reduced perioperative mortality below 10% in high volume centers. However, PD is associated with considerable morbidity (40-58.5%) like postoperative pancreatic fistula, delayed gastric emptying, biliary fistula, postoperative hemorrhage, and pulmonary complications.

Several surgical techniques and perioperative care have been described to prevent or reduce the incidence of pancreatic fistula after PD, including reconstruction of the digestive tract with pancreaticogastrostomy, duc-to-mucosa reconstruction or pancreaticojejunostomy by intussusception, use of somatostatin and prophylactic analogues, the use of stents in the main pancreatic duct, and use of different sealants.

Although perioperative morbidity and mortality associated with PD have improved significantly over the years, even in high-volume centers, the incidence of postoperative fistula remains at 9.9-28.5%. Therefore, the ideal pancreatic reconstruction technique that prevents fistula is not yet available.

The use of sealants has been one of the approaches taken to try to reduce the rate of fistulas. Some uncontrolled or non-randomized studies have shown that the use of fibrin glue-based adhesives in combinations with felting patches can lead to a B / C grade fistula rate of 0-10%. Only 2 randomized clinical trials have been performed with fibrin glue, with opposite results in terms of significant reduction of pancreatic fistula.

Hemopatch is a patch consisting of a soft, thin and flexible pad of collagen derived from the bovine dermis, coated with NHS-PEG (pentaerythritol polyethylene glycol ether tetra-succinimidyl glutarate). It is intended to be a surgical sealant for procedures in which control of leakage by conventional surgical techniques is ineffective or impractical, making it a plausible option to use during PD in order to decrease postoperative pancreatic fistula.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients scheduled for pancreatoduodenectomy by open approach, depending on the diagnosis/nature of the tumor.
  • ASA score < 4.
  • Male and female patients ≥ 18 and ≤ 80 years of age.
  • With the consent form signed.

Exclusion criteria

  • Patients scheduled for pancreatoduodenectomy by open approach, depending on the diagnosis/nature of the tumor.
  • ASA score < 4.
  • Male and female patients ≥ 18 and ≤ 80 years of age.
  • With the consent form signed.

Treatment and study plan

HEMOPATCH

Device

Collagen patch derived from bovine dermis, coated with NHS-PEG, applied covering the pancreaticojejunostomy after pancreatoduodenectomy once the anastomosis is completed.

Primary outcomes

  1. Postoperative type B and C pancreatic fistula

    Time frame: Up to 3 months

    Postoperative type B and C pancreatic fistula rate defined according to the International Study Group of Pancreatic Fistula criteria, measured by amylases and/or lipases levels in the perianastomotic drainage

Secondary outcomes

  1. Hospital stay

    Time frame: Up to 3 months

    Days of duration

  2. Stay in intensive care unit

    Time frame: Up to 3 months

    Days of duration

  3. Total postoperative fistula (including type A, B, and C)

    Time frame: Up to 3 months

    Percentage of patients

  4. Reoperations including interventional radiology

    Time frame: Up to 3 months

    Percentage of patients

  5. Delayed gastric emptying

    Time frame: Up to 3 months

    Percentage of patients

  6. Biliary fistula

    Time frame: Up to 3 months

    Percentage of patients

  7. Hemorrhage

    Time frame: Up to 3 months

    Percentage of patients

  8. Deep organ space complications

    Time frame: Up to 3 months

    Deep organ space complications

  9. Death, irrespective of cause

    Time frame: Up to 3 months

    Death

  10. Overall complications (according to Clavien-Dindo classification)

    Time frame: Up to 3 months

    Percentage of patients

Sponsors and collaborators

Lead sponsor

Hospital Miguel Servet

Other

Collaborators

  • Aragon Health Science Institute

Registry information

Official study title

Use of Hemopatch as a Sealant at the Pancreaticojejunostomy After Pancreatoduodenectomy to Prevent Postoperative Pancreatic Fistula

Important dates

Study start
2018
Primary completion
2020
Study completion
2022
First posted
Feb 5, 2018
Registry last updated
Feb 11, 2022

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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