CompletedPhase 4

A Comparison of the Sedation During Endoscopy in Children

238 participantsStarted 2015-01

Plain-language summary

The primary aim of this study was to investigate the efficiency and safety of midazolam plus ketamine versus fentanyl plus propofol administered to children undergoing UGE and to determine the most appropriate sedation protocol.

Who can participate

Age range4 Years – 17 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * All the patients were in ASA (American Society of Anesthesiologists) physical status I or II. Exclusion Criteria: * Patients with respiratory tract infections, glaucoma, psychosis, porphyria, hypertension, metabolic or neurologic diseases, increased intracranial pressure and intracranial mass, and patients known to be allergic to the drugs used were excluded from the study.

What they're measuring

the effectiveness of sedation

Timeframe: six months

Trial details

NCT IDNCT02732132

SponsorKanuni Sultan Suleyman Training and Research Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2015-07

View on ClinicalTrials.gov More Failed Moderate Sedation During Procedure trials