Treatment of acute oral herbicide poisoning with medicinal charcoal granules: a prospective multi-center real-world study

Status

Active, not recruiting

Phases

Phase 4

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2400090823

Enrollment

Unknown

Registered

2024-10-14

Start date

2024-11-01

Completion date

Unknown

Last updated

2024-10-21

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

Conditions

acute oral herbicide poisoning

Interventions

Out-patient Group:None

In-hospital Group:None

Eligibility

Sex/Gender

All

Age

14 Years to 100 Years

Inclusion criteria

Inclusion criteria: ? Patients with acute oral herbicide poisoning; ? Age =14 years old; ? Informed consent was obtained from patients or their guardians. ? If the patient has disturbance of consciousness, the drug can be administered through an indwelling gastric tube with airway protection and the informed consent of the guardian.

Exclusion criteria

Exclusion criteria: ? Non-oral herbicide poisoning; ?Exposure to toxins that inhibit gastrointestinal peristalsis (such as anticholinergic drugs, opioids, etc.); ? Disturbance of consciousness, no swallowing reflex, no airway protection; (4) Gastrointestinal corrosion or bleeding, gastrointestinal damage or suspected perforation; ? Recurrent vomiting; ? Informed consent could not be obtained.

Design outcomes

Secondary

Measure	Time frame
Serum herbicide concentration;blood routine examination;liver and kidney function test, and biochemistry;Coagulation function;Myocardial marker;	—

Primary

Measure	Time frame
mortality rate;	—

Countries

China

Contacts

Public ContactFeng Baobao

Shandong Provincial Hospital Affiliated to Shandong First Medical University

robert_feng@163.com+86 159 6605 3097

Outcome results

None listed

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