Skip to content

Using the hemostatic agents in submucosal injection of endoscopic submucosal dissection: a multicenter observational study

Using the hemostatic agents in submucosal injection of endoscopic submucosal dissection: a multicenter observational study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800016341
Enrollment
Unknown
Registered
2018-05-25
Start date
2018-07-01
Completion date
Unknown
Last updated
2018-05-28

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

Conditions

early digestive tract tumor

Interventions

epinephrine group:Using epinephrine in submucosal injection
Hemocoagulase group:Using hemocoagulase in submucosal injection

Sponsors

Changhai hospital, Second Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 75 years old,males or females; 2. Patients with superficial tumor of the esophagus, stomach or colon underwent ESD; 3. Cardiopulmonary function is suitable for ESD and no coagulation system diseases; 4. Hb, PLT, PT, INR and APTT reached ESD indication; 5. Freely given informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with mental and neurological diseases, serious cardiopulmonary diseases, liver and kidney diseases, immune and hematological diseases, or other serious diseases that affect their survival (such as cancer, AIDS, etc.); 2. Coagulation disorders (including thrombocytopenia, hemophilia, von Willebrand disease), or those who use anticoagulants or antiplatelet drugs could not be discontinued; 3. Risk factors for thrombosis (such as long-term bed-ridden, history of venous thrombosis, etc.); 4. Patients allergic to the product or a product of the same kind; 5. Planning pregnancy, pregnant and breastfeeding women; 6. Patients joined in other clinical trials 3 months before ESD or during the trial period; 7. Other reasons inappropriately to participate in the trial.

Design outcomes

Primary

MeasureTime frame
Hemostasis effect in ESD;

Secondary

MeasureTime frame
bleeding after ESD;

Countries

China

Contacts

Public ContactLiu Feng

Changhai hospital, Second Military Medical University

drliuffeng@hotmail.com+86 13681973214

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026