Low Blood Pressure Clinical Trials

Find Low Blood Pressure Clinical Trials Near You

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

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
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
Participation Requirements
Sex: All
Minimum Age: 1
Maximum Age: 12
Healthy Volunteers: f
View:

• 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

Locations
Other Locations
China
Tongji Hospital
RECRUITING
Wuhan
Contact Information
Primary
Li Xu
li_xu717@hust.edu.cn
+862783663173
Time Frame
Start Date: 2026-06-15
Estimated Completion Date: 2028-12-01
Participants
Target number of participants: 180
Treatments
Experimental: Toddlers (1-3 years)
Experimental: Preschoolers (4-6 years)
Experimental: School-age (7-12 years)
Related Therapeutic Areas
Sponsors
Leads: Huazhong University of Science and Technology

This content was sourced from clinicaltrials.gov