Skip to content

Effect of combined treatment with volatile anesthetics, dexmedetomidine, and methylprednisolone on prognosis in patients undergoing heart valve surgery

Effect of combined treatment with volatile anesthetics, dexmedetomidine, and methylprednisolone on prognosis in patients undergoing heart valve surgery: a single-center, randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100043498
Enrollment
Unknown
Registered
2021-02-21
Start date
2021-03-01
Completion date
Unknown
Last updated
2021-06-07

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

Conditions

postoperative recovery and perioperative organ protection

Interventions

Intervention group:Intravenous methylprednisolone 120mg at anesthetic induction
Dexmedetomidine infusion at a rate of 0.4ug/kg/h after induction until the end of surgery
Volatile anesthetic to maintain anesthesia.
Control group:Use the same technique to give the same amount or rate of normal saline at the same time point mentioned above, and use total intravenous anesthesia (propofol) throughout the surgery to

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years; 2. Undergoing heart valve surgery with cardiopulmonary bypass; 5. Written inform consent.

Exclusion criteria

Exclusion criteria: 1. Heart rates < 50 beats per min, sick-sinus syndromes, second-degree or above atrioventricular block; a myocardial infarction within 7 days, left ventricular ejection fraction <30%, use of clonidine to treat hypertension, hemodynamically significant arrhythmia; 2. Severe cerebral, hepatic, renal disease, a history of systematic infection in the preceding 30 days, a family history of malignant hyperthermia, insulin-treated diabetes; 3. A history of allergy to any of the study drugs, or exposure to any of the study drugs within 30 days; 4. Pregnant or breast-feeding; 5. Participation in another experimental protocol at the time of intervention selection; 6. Refused to cooperate or be inappropriate.

Design outcomes

Primary

MeasureTime frame
Days at home up to 30 days after surgery (DAH30);

Secondary

MeasureTime frame
Major adverse cardiovascular cerebral event (MACCE);Postoperative acute kidney injury;5-level EQ-5D score;Postoperative mortality;Length of ICU stay;Duration of mechanical ventilation after surgery;Length of postoperative hospital stay;Hospitalization cost;Peak blood glucose;New atrial fibrillation;

Countries

China

Contacts

Public ContactHai Yu
yuhaishan117@yahoo.com+86 18980601548

Outcome results

None listed

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