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Cardioprotective effect of dexmedetomidine in patients undergoing cardiac valve replacement with cardiopulmonary bypass

Cardioprotective effect of dexmedetomidine in patients undergoing cardiac valve replacement with cardiopulmonary bypass

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100044370
Enrollment
Unknown
Registered
2021-03-17
Start date
2021-04-01
Completion date
Unknown
Last updated
2021-09-07

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

Conditions

Valvular heart disease

Interventions

Group CON:Give an equal volume of 0.9% sodium chloride injection for continuous pumping
Group DEX:A load dose of dexmedetomidine 1 µg/kg was given within 10 minutes before induction, and then 0.5 µg/kg/h was continuously pumped to the end of operation.

Sponsors

First Affiliated Hospital of Kunming Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 50 Years

Inclusion criteria

Inclusion criteria: Aged 30-50 years, BMI index 18-25 kg/m2, ASA grade III-IV, NYHA grade II-III, LVEF>40%, planned to electively undergo heart valve replacement surgery under general anesthesia and cardiopulmonary bypass. Had no previous history of cardiac surgery and heart failure, and no myocardial infarction was found in the past month.

Exclusion criteria

Exclusion criteria: Bradycardia (HR= Grade IV; emergency surgery; severe infection; multiple organ diseases, such as liver, kidney, lung, musculoskeletal disease or immune system disease; patients allergic to dexmedetomidine.

Design outcomes

Primary

MeasureTime frame
Systolic blood pressure, SBP;heart rates, HR;Complete Blood Count;Tryptase, TPS;cTnI;

Countries

China

Contacts

Public ContactQian Jinqiao

The First Affiliated Hospital of Kunming Medical University

qianjinqiao126@126.com+86 18288957801

Outcome results

None listed

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