Dexmeditomidine-ketamine sedation versus ketamine-midazolam sedation in pediatrics with surgically uncorrected TOF undergoing cardiac multi-slice spiral CT

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

PACTR

Registry ID

PACTR201906664920036

Enrollment

Registered

2019-06-10

Start date

2019-03-18

Completion date

Unknown

Last updated

2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Paediatrics

Interventions

dexmedetomidine ketamine

ketamine midazolam

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: paediatric patients 2-3 years old, (ASA) physical status III with surgically uncorrected TOF scheduled for multi-slice spiral computed tomography

Exclusion criteria

Exclusion criteria: active chest infection, renal impairement, parent refusal to participate hypersensitivity to study drugs any contraindication to the study drugs were excluded.

Design outcomes

Primary

Measure	Time frame
the recovery time for all patients (The elapsed time for the participant to open his eyes upon command after discontinuation of the study drug).	—

Secondary

Measure	Time frame
sedation scores;systolic and diastolic blood pressures;postoperative complications;additional doses of ketamine;intraoperative complications as hypoxia	—

Countries

Egypt

Contacts

Public ContactAmr kasem

lecturer of Anesthesiology

amr240@gmail.com00201005282224

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026