CompletedPhase 4ketamine

A Comparison of the Sedation During Endoscopy in Children

Sponsored by Kanuni Sultan Suleyman Training and Research Hospital

NCT ID
NCT02732132
Target Enrollment
238 participants
Start Date
2015-01
Est. Completion
2015-09

About This Study

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.

Conditions Studied

Failed Moderate Sedation During Procedure

Interventions

  • Ketamine and Midazolam
  • Propofol and Fentanyl

Eligibility

Age:4 Years - 17 Years
Healthy Volunteers:No
View full eligibility criteria
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.

This trial is not recruiting

This study has completed enrollment. Check back for results or find similar trials.

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Data Source
ClinicalTrials.gov

Last updated from source