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NCT04376541

Fast Tracking Impact on Fentanyl Consumption and Parents Satisfaction

Completed Last updated 6 May 2020
What this trial tests

trial testing Fentanyl in Fentanyl Adverse Reaction in 70 participants. Completed in 1 April 2020.

Timeline
1 January 2016
Primary endpoint
1 April 2020
1 April 2020

Quick facts

Lead sponsorAin Shams University
StatusCompleted
Study typeOBSERVATIONAL
Enrollment70
Start date1 January 2016
Primary completion1 April 2020
Estimated completion1 April 2020

Drugs / interventions tested

Conditions studied

Sponsor

Ain Shams University

Who can join

Adults 3 Months to 18, any sex, with Fentanyl Adverse Reaction or Caudal Anesthesia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The investigators are measuring fentanyl consumption in micrograms used during anesthesia for patients on fast track congenital cardiac surgeries

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other trials of Fentanyl

Trials testing the same drug.

Other Ain Shams University trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04376541.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing