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Clinical Trials in China / NCT07697404
Recruiting Phase 4

The ED95 of Ciprofol for Laryngeal Mask Airway Insertion With Fentanyl in Children: A Biased-Coin Dose-Finding Trial

NCT07697404 · tracked via the Priya Life Science China tracker
Sponsor
Huazhong University of Science and Technology
Phase
Phase 4
Started
2026-06-15
Last updated
2026-07-13

Condition(s) studied

PediatricAnesthesia InductionCiprofolLaryngeal Mask Airway

Investigational drug(s) / intervention(s)

CiprofolFentanyl

Ciprofol: All patients will receive a fixed dose of fentanyl (1 μg/kg) and a predetermined bolus dose of ciprofol, administered intravenously over 1 minute. The initial ciprofol dose is set at 0.35 mg/kg, with a dose step size of 0.1 mg/kg. The dose for each subsequent patient is determined by the biased-coin design: if the previous patient achieves successful LMA insertion (no movement), the next patient receives the same dose with a probability of 0.947 or a 0.1 mg/kg lower dose with a probability of 0.053. If the previous patient fails (movement occurs), the next patient receives a 0.1 mg/kg higher dose.

Fentanyl: All patients will receive a fixed dose of fentanyl (1 μg/kg) and a predetermined bolus dose of ciprofol

Study summary

Ciprofol is a novel intravenous anesthetic with a pharmacological profile similar to propofol but with a lower incidence of injection pain, hypotension, and respiratory depression. For pediatric day-case surgeries, laryngeal mask airway (LMA) insertion without neuromuscular blockers is increasingly preferred. While opioids are often combined with hypnotics to optimize insertion conditions, the optimal bolus dose of ciprofol when co-administered with a standard dose of fentanyl for LMA insertion in children remains unknown. This study aims to determine the 95% effective dose (ED95) of a single intravenous bolus of ciprofol, combined with a fixed dose of fentanyl (1 μg/kg), for successful LMA insertion in children aged 1-12 years during general anesthesia induction.

Eligibility

Sex
ALL
Min age
1 Year
Max age
12 Years
Healthy volunteers
No
Inclusion Criteria: * American Society of Anesthesiologists (ASA) physical status I or II * Aged 1 to 12 years * Scheduled for elective surgery requiring general anesthesia with laryngeal mask airway (LMA) insertion (e.g., ophthalmic surgery, skin lesion excision, minor abdominal or urological procedures, with expected surgical duration ≤ 2 hours) * Written informed consent obtained from parents or legal guardians Exclusion Criteria: * Known allergy or hypersensitivity to ciprofol, fentanyl, or any study-related drugs * Intellectual disability, cognitive-affective disorders, psychiatric or neurological diseases * Inability to cooperate with peripheral intravenous cannulation * History of reactive airway disease or suspected difficult airway * Body mass index (BMI) ≥ 30 kg/m² or ≤ 15 kg/m² * History of sedative medication use * Inability to understand the study protocol or participation in another clinical trial within the past 30 days

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Tongji Hospital Wuhan Hubei Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07697404 on ClinicalTrials.gov ↗ ← All trials in China