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Clinical validation of gene targets for dexmedetomidine adverse reactions

Clinical validation of gene targets for dexmedetomidine adverse reactions

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500105507
Enrollment
Unknown
Registered
2025-07-04
Start date
2025-07-15
Completion date
Unknown
Last updated
2025-07-07

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

Conditions

Nervous system disease

Interventions

The dexmedetomidine group:Administering dexmedetomidine by infusion before anesthesia induction

Sponsors

Liuzhou Workers' Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. Age: between 18 and 55 years old, gender not restricted; 2. ASA I-II grade, BIM 20-35 kg/m^2 3. Patients requiring surgery anesthesia with dexmedetomidine; 4. Voluntary participation in this study and signing the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Suffering from severe liver or kidney dysfunction (liver function classified as Child-Pugh grade C, creatinine clearance rate < 30 ml/min); 2. Having severe cardiovascular diseases (such as unstable angina pectoris, acute phase of myocardial infarction, severe heart failure, etc.); patients with sinus bradycardia or atrioventricular block; 3. Having a history of mental illness or cognitive dysfunction and unable to cooperate in completing the relevant assessment; 4. Allergic to dexmedetomidine or its excipients; 5. Having used dexmedetomidine recently (within 3 months) or using drugs that may affect the metabolism of dexmedetomidine or have interactions.

Design outcomes

Primary

MeasureTime frame
Gene target;

Countries

China

Contacts

Public ContactZhang Yanzhuo

Liuzhou Workers' Hospital

Zhangyanzhuo625@sina.com+86 136 0772 7755

Outcome results

None listed

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