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The application of smectite in postoperative bleeding after colorectal polyp surgery

The application of smectite in postoperative bleeding after colorectal polyp surgery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600118505
Enrollment
Unknown
Registered
2026-02-06
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-02-09

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

Conditions

Digestive system disease

Interventions

Trial group:The patient received intravenous administration of snake venom thrombin (twice daily, 1 unit each time, for 72 hours) in combination with oral administration of smectite powder, three time
Control group:The patient received intravenous administration of snake venom thrombin, twice daily, 1 unit each time, for 72 hours.

Sponsors

The First Affiliated Hospital with Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18 - 70 years old 2. Colorectal polyps, treated by endoscopic methods; 3. Fresh red bloody stool; 4. Preoperative hemoglobin stable, postoperative hemoglobin decreased by more than 3g/dL compared to preoperative level; 5. Good patient compliance, able to accept long-term follow-up; 6. No coagulation dysfunction, no history of mental illness; 7. No severe underlying diseases such as heart or lung conditions, able to tolerate anesthesia and surgery.

Exclusion criteria

Exclusion criteria: 1. Severe bleeding volume (>1000ml), with occurrence of hemorrhagic shock (blood pressure < 90/60mmHg) and other conditions; 2. Occurrence of perforation, infection and other situations; 3. Bleeding caused by other reasons such as hemorrhoids, diverticula, vascular malformations, etc.; 4. Allergic to montmorillonite and snake venom thrombin; 5. History of colorectal tumors, undergoing radiotherapy and chemotherapy; 6. Presence of severe organic diseases, coagulation dysfunction and other conditions that cannot tolerate surgery; 7. Patients who are unwilling to receive experimental treatment or cannot cooperate with follow-up.

Design outcomes

Primary

MeasureTime frame
The 24-hour hemostasis rate after treatment;

Secondary

MeasureTime frame
Frequency of hematochezia;The amount of bleeding;Change in Hb level;

Countries

China

Contacts

Public ContactLiu Li

The First Affiliated Hospital with Nanjing Medical University

liulivip9178@163.com+86 158 5056 0622

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026