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Role of Hemostatic Powder (Endo-clotTM) in Success and Prevention of Bleeding Within Gastric Cancer Patients With Bleeding

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02732483
Enrollment
32
Registered
2016-04-08
Start date
2016-04-30
Completion date
2018-04-30
Last updated
2016-04-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bleeding at Gastric Cancer

Keywords

gastric cancer, bleeding, gastrointestinal hemorrhage

Brief summary

Gastrointestinal(GI) hemorrhage related with gastric cancer is prevalent in advanced cases mostly. As endoscopic hemostatic methods such as argon plasma ablation (APC) had developed, controlling GI hemorrhage in gastric cancer is much easier these days. but re-bleeding rate is still high, even after successful hemostasis with APC or electrical coagulation. Furthermore patients who were experienced re-bleeding are expected poorer survival outcomes than those who are not. So excellent bleeding control in gastric cancer is most important in GI hemorrhage of gastric cancer. Recently developed hemostatic powder \[Endo-Clot(TM)\] is easy to use and have proven its usefulness in GI hemorrhage in peptic ulcer diseases. So in this study, investigator will try to find out feasibility & safety of Endo-Clot(TM) in GI hemorrhage in gastric cancer.

Interventions

The patients agreed in this study, bleeding control will going to be done with Endo-Clot(TM)

Sponsors

Yonsei University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
19 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Age over 19 and less 80 yeas old * Gastric cancer was diagnosed with biopsy and/or computed tomography * Endoscopic hemostasis is needed upto GI hemorrhage * Endoscopic examination is available in 24hours * ECOG performance status(PS) \<2

Exclusion criteria

* Double primary caner * Hypersensitivity of hemostatic power\[Endo-Clot(TM)\] * Variceal bleeding or benign gastric ulcer bleeding * Hemodynamically unstable with low systolic BP\<90mmHg and/or tachycardia PR\>120bpm * endoscopic hemostasis within 7 days before screening * Contraindication for endoscopic examination * Pregnant * Breast feeding * bleeding tendency with low platelet count \<50,000 /mm\^3 and/or INR\>2 * Bacterial infection with needs for antibiotics therapy * Unavailable to discontinue anti-coagulation agent for 3days * Vascular shunt * Cardiovascular and/or pulmonary diseases * Active hepatitis or severe liver diseases * Renal dysfunction * Bone marrow dysfunction * Neurologic deficit and/or psychotic feature * Unavailable informed consent

Design outcomes

Primary

MeasureTime frameDescription
Rebleeding ratewithin 30 daysProportion of patients who are experience rebleeding events after hemostasis within 30 days expected to be lower than 10 %. Definition rebleeding events 1. Overt symptoms of GI bleeding(such as hematemesis, melena) and/or Hemoglobin down more than 2g/dl compared to Hemoglobin level which were checked just after procedure.

Secondary

MeasureTime frameDescription
Success of bleeding control ratewithin 2 weeks and 4 weeksProportion of patients who are experience successful hemostasis is expected to be higher than 80 %applying Endo-Clot™, Rebleeding rate in 3days, rate of additional intervention other than initial endoscopic hemostasis, Mortalities
Rebleeding ratein 3 daysProportion of patients experience rebleeding events after hemostasis within 3 days expected to be lower than 5 %. Definition of Rebleeding rate in 3days 1. Overt symptoms of GI bleeding(such as hematemesis, melena) and/or Hemoglobin down more than 2g/dl compared to Hemoglobin level which were checked just after procedure.
Rate of additional intervention other than initial endoscopic hemostasiswithin 2 weeks to 4 weeksDefinition of Successful hemostasis; controlled bleeding vessel in 5 minute after applying Endo-Clot™
Mortalitieswithin 2 weeks to 4 weeks

Countries

South Korea

Contacts

Primary ContactJun Chul Park, MD
JUNCHUL75@yuhs.ac+ 82-2-2228-2272

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026