Pancreatic Tumor Clinical Trial
Official title:
Randomized Controlled Study to Evaluate the Effect of Thrombin-containing Collagen-based Hemostatic Matrix on Prevention of Pancreatic Fistula After Pancreatecomy
Under the hypothesis that collagen-based hemostatic agents improve the suppression of leakage
of hemostatic pancreatic fluid at the surgical site during surgery, thrombin-containing
collagen-based hemostatic agents are applied in surgery in patients with pancreatectomy. The
investigators intend to evaluate the effectiveness of collagen-based hemostatic agents
containing thrombin through clinical evaluation of hemostatic effect and anti-leakage effect
of pancreatic fluid.
This clinical study is a study for comparative evaluation of hemostasis and anti-leakage
effect of bile or pancreatic fluid when applied after pancreatic resection of a
collagen-based hemostatic agent containing thrombin. It is prospective, single center,
randomized, and non-inferiority test. Participants are patients who are diagnosed with
pancreatic disease and other diseases, and plan to undergo pancreatectomy. Through the
randomization, in the case of the intervention group, after the pancreatectomy, the Collastat
(CollaStat®, Dalim Tissen. Co., Ltd., Korea) is applied to the cut surface, and in the case
of the control group, Collaseal (CollaSeal®, Dalim Tissen. Co., Ltd., Korea) is applied. In
this study, 30 participants were required for each intervention group and control group.
After surgery, the participants is hospitalized for 7 days and undergoes follow-up
observation. Pancreatic leakage is measured through the drainage tube before discharge and
evaluated as biochemical leakage (BL), B, or C according to the definition of International
Study Group for Pancreatic Fistula (ISGPS).
The primary endpoint of this study was the prevention rate of leakage. The postoperative
pancreatic fistula (POPF) was defined according to the definition of ISGPS. Secondary end
point was assessed as the difference between groups of total number of collagen hemostatic
agents used, hospital length of stay and number of patient who received RBC transfusion.
Safety was assessed based on the incidence of adverse events occurred.
1. Synopsis
- Title: Randomized controlled Study to evaluate the Effect of Thrombin-containing
Collagen-based Hemostatic Matrix on Prevention of Pancreatic fistula after
Pancreatectomy
- Study center: Single center from Korea
- Study type: Single center prospective randomized controlled study
- Planned study dates: February 2018 to September 2020
2. Objectives
■ The aim of this study was to evaluate the safety and efficacy of flowable thrombin
containing collagen hemostat matrix (T-C matrix) over the thrombin coated L-dopa
contained collagen patch (T-CD patch) on clinical outcomes including PPH and POPF as a
randomized controlled clinical trial.
3. Background
- Hemostasis is the most basic and important procedure as a treatment for bleeding
that inevitably follows most surgical procedures. Recently, with the development of
pancreatic surgery and postoperative management, the mortality rate associated with
surgery has decreased significantly, but the rate of complications due to massive
bleeding or leakage of pancreatic fluid during surgery has not changed
significantly. In hepatobiliary and pancreas (HBP) surgery, post-pancreatectomy
hemorrhage (PPH) and postoperative pancreatic fistula (POPF) are both the main
source of major morbidity and mortality.
- Collagen is a natural substrate for various kinds of animal cells, and contains a
relatively large amount compared to other proteins in animal tissues, and can be
easily extracted and purified from animal tissues. Collagen not only has low
antigenicity, but also has excellent hemostatic effect and cell attachment ability,
so it is often used as a major component of hemostatic agents and artificial tissue
substitutes. In addition, collagen provides an environment in which fibroblasts can
be produced and induces wound healing by inactivating elastase and matrix
metalloproteases (MMPs).
- The investigators developed a novel flowable thrombin containing collagen hemostat
matrix (T-C matrix) having flowable paste-like form. The T-C matrix consists of two
connectable syringes, one of which contains collagen granules and thrombin, and the
other contains calcium chloride (CaCl2) solution. Due to the flowable
characteristic of the resultant matrix, T-C matrix can be easily applicable to
irregular surface such as surgical site where anastomotic leakage is a concern.
Currently, thrombin /coated L-3,4-dihydroxyphenylalanine (L-dopa DOPA) contained
collagen patch (T-CD patch) are using on prevention of leakage and bleeding in
pancreatic surgery. Although L-DOPA is known to contribute to adhesiveness which
facilitates application of T-CD patch on wound sites, there are some controversial
studies that L-DOPA have cytotoxicity and may induce inflammatory reaction with a
high dose.
4. Methodology
- The clinical study was designed to evaluate the effect of T-C matrix on the
prevention of leakage in a pancreatectomy. The expected number of participants is
60.
- This clinical study is a randomized prospective comparative study of the outcome
according to the hemostat materials as a non-inferiority test, and the research
hypothesis is as follows.
√ Null Hypothesis: There is no difference in the incidence of POPF between patients
who were applied TC matrix (CollaStat®, Dalim Tissen. Co., Ltd., Korea) and T-CD
patch (CollaSeal®, Dalim Tissen Co. Ltd., Korea) after pancreatectomy.
- In the case of evaluating the incidence of POPF after pancreatectomy, the results
of previous studies of the 'leakage' ratio showed a leak prevention effect (θA) =
88% of the existing treatment method of CollaSeal® analog (Montorsi M et al. 2012).
The new treatment effect (θT) is intended to demonstrate non-inferiority that does
not exceed the non-inferiority limit (δ) compared to the existing treatment effect
(θA). The non-inferiority limit (δ) was calculated by more than 75% of the existing
treatment effect. The non-inferiority limit was calculated to be 0.22 based on the
case where more than 75% of the 88% of the existing treatment method is confirmed,
that is, the treatment success rate is more than 66%. It was decided that
CollaStat® was non-inferior to CollaSeal® when the lower limit of the 95% CI for
the difference between the two groups was greater than -0.22. If the allocation
ratio between the two groups is 1: 1 and the first-class error α = 5% and the
second-class error β = 20%, considering the dropout rate of 10%, 30 study groups
and control groups each need 30 subjects.
- The random assignment of this study is assigned according to the order of
assignment in the planning stage of the study as a block randomization scheme with
appropriate block size set.
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