CompletedN/Aketamine

Efficacy and Safety of Continuous Infusion of Ketamine in Pediatric Intensive Care Unit (KISS Study)

Sponsored by Azienda Ospedaliera di Padova

NCT ID
NCT04427605
Target Enrollment
57 participants
Start Date
2019-04-01
Est. Completion
2021-09-01

About This Study

This study, prospectively evaluate the efficacy and safety of ketamine administered in continuous infusion lasted more than 12 hours in children admitted to Pediatric Intensive Care Unit of Padova. This drug may be used as adopted as adopted as adjuvant to analgesia and sedation or as adjuvant to bronchospasm therapy. The investigators evaluated efficacy considering the sparing of other analgesics and sedatives and the level of sedation after ketamine infusion for the first use and the sparing of other bronchospasm drugs sedative dosage for the second use. To evaluate safety the investigators considered the presence of adverse effects and onset of withdrawal and delirium syndrome. The study will included al least 55 pediatric patients \< 18 years and mechanically ventilated.

Conditions Studied

AnalgesiaKetamine ToxicityBronchospasmSedation Complication

Eligibility

Age:N/A - 18 Years
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

* pediatric intensive care unit admission
* mechanical ventilation
* ketamine infusion \> 12 hours

Exclusion Criteria:

* parents refusal to participate

Study Locations (1)

Azienda Ospedale Università Padova
Padova, PD, Italy

This trial is not recruiting

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

Find recruiting trials
Data Source
ClinicalTrials.gov

Last updated from source