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Pharmacokinetic studies of dexmedetomidine in elderly patients during anesthesia

Pharmacokinetic studies of dexmedetomidine in elderly patients during anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OCC-13003799
Enrollment
Unknown
Registered
2013-11-12
Start date
2013-11-15
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Surgical patients

Interventions

Sponsors

The Third Xiangya Hospital Of Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Local anesthesia patients aged 18-40 years and 65-75 years

Exclusion criteria

Exclusion criteria: 1. severe bradycardia (heart rate \50 beats/min); 2. uncompensatedacute circulatory failure at time of randomisation; 3. atrioventricular-conduction block II–III (unless pacemaker installed); 4. Patients with significant haematological, endocrine, metabolic, or gastrointestinal disease were excluded; 5. use of centrally acting a2 agonists or antagonists; 6. Patients with a history of intolerance to dexmedetomidine or related compounds and additives; 7. Subjects with human immunodeficiency virus (HIV), hepatitis B, hepatitis C; 8. Pregnancy, lactation Women; 9. Patients with donation of blood or collection of plasma sample in 3 months before the dose of the study; 10. investigators' own judgement.

Design outcomes

Primary

MeasureTime frame
Blood Drug Concentration;

Countries

China

Contacts

Public ContactGuoping Yang, Kaiming Duan, Saiying Wang

The Third Xiangya Hospital Of Central South University

ygp9880@163.com+86 0731 88618339

Outcome results

None listed

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