🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Writer Login
Latest
Clinical Trials in China / NCT05634057
Recruiting Not applicable

Efficacy of Anisodamine Hydrobromide Combined With Low-molecular-weight Heparin in the Treatment of Patients With Sepsis

NCT05634057 · tracked via the Priya Life Science China tracker
Sponsor
Chen Ying
Phase
Not applicable
Started
2024-01-25
Last updated
2025-05-21

Condition(s) studied

Sepsis

Investigational drug(s) / intervention(s)

Anisodamine hydrobromide combined with heparin

Anisodamine hydrobromide combined with heparin: The anisodamine hydrobromide combined with heparin treatment group is on the basis of conventional treatment.

Study summary

The study aimed to investigate the effectiveness of anisodamine hydrobromide combined with heparin in the treatment of patients with critical infection, in the hope that the therapy will provide alternatives to the treatment of patients with critical infection.

Eligibility

Sex
ALL
Min age
18 Years
Max age
110 Years
Healthy volunteers
No
Inclusion criteria: 1. Age greater than 18 years; 2. Meets the diagnostic criteria for sepsis according to the "Sepsis-3" ; 3. Patient or their legal representative consents to treatment and signs an informed consent form. Exclusion criteria: 1. Patients expected to die within 24 hours after enrollment; 2. Contraindications to low molecular weight heparin and scopolamine butylbromide drugs; 3. Patients with thrombotic diseases requiring treatment with low molecular weight heparin; 4. Patients with terminal-stage malignancies, severe immunodeficiency, immunosuppression, severe liver or kidney dysfunction (defined as liver or kidney SOFA score ≥ 3 points), etc.; 5. Pregnant and lactating women; 6. Patients participating in other clinical trials.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Beijing Chaoyang Hospital, Capital Medical University Beijing China Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05634057 on ClinicalTrials.gov ↗ ← All trials in China