Actively Recruiting

Phase 2
Phase 3
Age: 3Years - 17Years
All Genders
NCT07036419

A Trial of Remimazolam for Intraoperative Sedation in Pediatric and Adolescent Patients

Led by Jiangsu HengRui Medicine Co., Ltd. · Updated on 2026-02-18

240

Participants Needed

1

Research Sites

42 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The study is being conducted to evaluate the efficacy and safety of Remimazolam for intraoperative sedation in pediatric and adolescent patients.

CONDITIONS

Official Title

A Trial of Remimazolam for Intraoperative Sedation in Pediatric and Adolescent Patients

Who Can Participate

Age: 3Years - 17Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Able and willing to provide a written informed consent.
  • Subjects requiring elective general anesthesia surgery.
  • Male or female.
  • Meet the weight standard.
Not Eligible

You will not qualify if you...

  • Pediatric patients scheduled for elective cardiothoracic, neurosurgical, or hepatic surgery.
  • Patients planned to receive anesthetic techniques other than total intravenous anesthesia (TIVA) during surgery.
  • Patients with medical history or evidence increasing sedation or anesthesia risk deemed unsuitable by the investigator.
  • Patients with history of asthma or risk for difficult mask ventilation or intubation.
  • Patients with clinically significant abnormal laboratory test values.
  • Known intolerance or allergy to benzodiazepines, propofol, opioids, neuromuscular blocking agents, or components.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Shanghai Children's Medical Center Affiliated to Shanghai Jiao Tong University School of Medicine

Shanghai, Shanghai Municipality, China, 200433

Actively Recruiting

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Research Team

L

Lei Tang

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

2

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