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Comprehensive optimization of desflurane anesthesia strategy in pediatric laparoscopic surgery: a prospective randomized controlled trial

Comprehensive optimization of desflurane anesthesia strategy in pediatric laparoscopic surgery: a prospective randomized controlled trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068906
Enrollment
Unknown
Registered
2023-03-01
Start date
2023-03-01
Completion date
Unknown
Last updated
2023-05-22

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

Conditions

Hernia, hydrocele, cryptorchidism and other diseases

Interventions

Control group:0.7MAC desflurane combined with remifentanil 10µg/(kg/h) was used to maintain anesthesia
Experimental group A:Dexmedetomidine 1µg/kg was intravenously injected before anesthesia induction, and 0.7MAC desflurane combined with 0.5µg/(kg/h) dexmedetomidine was used to maintain anesthesia
Experimental group B:Dexmedetomidine 1µg/kg was intravenously injected before anesthesia induction, and desflurane 1MAC combined with dexmedetomidine 0.5µg/(kg/h) was used for anesthesia maintenance
Experimental group C:Dexmedetomidine 1µg/kg was administered intravenously before induction of anesthesia, and desflurane 1MAC was used for maintenance of anesthesia
Experimental group D:Dexmedetomidine 1µg/kg was administered intravenously before induction of anesthesia, and 1.3MAC desflurane was used for maintenance of anesthesia

Sponsors

Department of Anesthesiology, the Sixth Affiliated Hospital of Harbin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1. ASA grade ?-?; 2. BMI<=30 (kg/m^2); 3. Aged between 5 and 12 years; 4. Children undergoing laparoscopic surgery; 5. The operation time is less than two hours.

Exclusion criteria

Exclusion criteria: 1. Patients with high risk of perioperative respiratory adverse events (recent history of upper respiratory tract infection, abnormal chest radiographs or abnormal blood images, malformation or dysplasia of respiratory tract or lung organs); 2. Patients with abnormal liver and kidney function or congenital heart disease; 3. Pneumoperitoneum intolerance; 4. Obvious mental retardation; 5. Suspected allergy to the drug in the study; 6. There are contraindications to regional block (abnormal coagulation status, hemorrhagic disease, local infection, etc.).

Design outcomes

Primary

MeasureTime frame
Hemodynamic measures;Indicators of early recovery time;

Secondary

MeasureTime frame
Indicators of adverse events in postoperative PACU;Indicators of health economic benefits;

Countries

China

Contacts

Public ContactYang Wanchao

Department of Anesthesiology, the Sixth Affiliated Hospital of Harbin Medical University

dachao_1980@126.com+86 137 9663 6010

Outcome results

None listed

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