Skip to content

Clinical Study of Anisodamine Hydrobromide or Atropine in Combination with Neostigmine

Clinical Study of Anisodamine Hydrobromide or Atropine in Combination with Neostigmine

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300074169
Enrollment
Unknown
Registered
2023-08-01
Start date
2023-08-01
Completion date
Unknown
Last updated
2025-02-24

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

Conditions

Sinus Tachycardia

Interventions

Anisodamine hydrobromide treatment group (Group N):Anisodamine hydrobromide antagonizes the bradycardic effect of neostigmine
Atropine control group (Group N): Atropine antagonizes the bradycardic effect of neostigmine

Sponsors

The Second Xiangya Hospital of Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-60 years old, any sex, ASA classification Level I-II; 2. Participants undergoing surgical procedures under general anesthesia with tracheal intubation; 3. Electrocardiogram in sinus rhythm; 4. Ethical, voluntary and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Participants with obvious abnormalities in preoperative electrocardiogram, inability to communicate normally, and inability to describe symptoms; 2. The electrocardiogram has arrhythmias (such as supraventricular arrhythmias or ventricular arrhythmias); 3. Previous history of severe cardiovascular disease or cardiac surgery; 4. History of neurological and urinary system diseases, liver and kidney diseases, and Sjogren's syndrome; 5. History and medical history of antiepileptic drugs, antiarrhythmic drugs, and other drugs known to affect electrocardiogram; 6. Severe electrolyte disorder; 7. Contraindications to neostigmine, anisodamine, and atropine; 8. Other possible reasons that may affect the study or reject participants.

Design outcomes

Primary

MeasureTime frame
Heart rate;

Secondary

MeasureTime frame
Adverse reactions (arrhythmia, thirst, dysuria);

Countries

China

Contacts

Public ContactCao Lijun

The Second Xiangya Hospital of Central South University

hivit1103@csu.edu.cn+86 159 7428 3099

Outcome results

None listed

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