Clinical trialPhase 2Completed
Intra-operative Application of HEMOPATCH to the Pancreatic Stump to Prevent Post-operative Pancreatic Fistula Following Distal Pancreatectomy
A Single-arm Phase II Trial of Intra-operative Application of HEMOPATCH to the Pancreatic Stump to Prevent Post-operative Pancreatic Fistula Following Distal Pancreatectomy
- Outcome
- Outcome unknown
- Phase
- Phase 2
- Status
- Completed
- Study type
- Interventional
- Start
- 13 August 2018
- Expected end
- 23 October 2020
- Enrollment
- 52 participants
- Sites
- 7
- Primary outcomes
- Number of Participants With a Clinically Significant Post-operative Pancreatic Fistula (POPF)
- Sponsor
- Other
- Results posted
- 2021-08-09
- Last update
- 3 November 2021
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Brief summary public domain (ClinicalTrials.gov)
Despite improvements and advances in pancreas surgery, about 30-35% of patients who have pancreas surgery develop a type of complication called a pancreatic fistula. A pancreatic fistula occurs when fluid produced by the pancreas leaks into the abdomen after pancreas surgery. Patients who develop a pancreatic fistula can have poor short-term and long-term consequences.We are studying the effect of a medical device named HEMOPATCH on the development and seriousness of pancreatic fistulas. HEMOPATCH is a thin, flexible bovine protein-based pad that may improve tissue sealing where it is applied during surgery. Some small studies called case studies of between 2 and 7 patients, and two clinical trials have shown that HEMOPATCH is effective at stopping bleeding and reducing drain output after some types of surgery. However, there have been no completed clinical trials using HEMOPATCH to prevent or reduce pancreatic fistulas in patients having pancreas surgery, so we don't know if it works in this setting. Health Canada has approved the use of HEMOPATCH as a device to stop bleeding or seal other bodily fluids for procedures in which the control of bleeding or leakage of other body fluids or air by standard surgical techniques are either ineffective or impractical.
Posted results (ClinicalTrials.gov registry) · primary outcome public domain (ClinicalTrials.gov)
Number of Participants With a Clinically Significant Post-operative Pancreatic Fistula (POPF) [Within 90 days post-operatively]. Count Of Participants, Participants. Hemopatch (n=52): 13.
Posted results (ClinicalTrials.gov registry) · secondary outcome public domain (ClinicalTrials.gov)
Number of Participants With a Post-operative Pancreatic Fistula (POPF) [Within 90 days post-operatively]. Count Of Participants, Participants. Hemopatch (n=52): 25.
Posted results (ClinicalTrials.gov registry) · secondary outcome public domain (ClinicalTrials.gov)
Number of Participants Who Experienced Post-Operative Complications [Within 90 days post-operatively]. Count Of Participants, Participants. Hemopatch (n=52): 14.
Posted results (ClinicalTrials.gov registry) · secondary outcome public domain (ClinicalTrials.gov)
90-Day Mortality Count [Within 90 days post-operatively]. Count Of Participants, Participants. Hemopatch (n=52): 2.
Posted results (ClinicalTrials.gov registry) · secondary outcome public domain (ClinicalTrials.gov)
Average Length of Stay in Hospital [Within 90 days post-operatively]. Median, days (Inter-Quartile Range). Hemopatch (n=52): 6 (4 to 8).
Papers 1
- Registry-listed results paperPATCH-DP: a single-arm phase II trial of intra-operative application of HEMOPATCH™ to the pancreatic stump to prevent p… DOI 10.1016/j.hpb.2021.05.007↗
The registry lists these as results papers; in a hand check of 27 such links about 78% reported the trial’s results, so read the paper before treating it as the outcome.