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Comparison of Dexmedetomidine as bolus or low â?? dose infusion to prevent postoperative agitation.

Dexmedetomidine as bolus or low â?? dose infusion for the prevention of emergence agitation with sevoflurane anesthesia in pediatric patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/10/016088
Enrollment
48
Registered
2018-10-22
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- AGE 2-12 YEARS Health Condition 2: N398- Other specified disorders of urinary system

Interventions

Intervention1: Comparative study: Comparison between 2 groups. GroupI(bolus dose of dexmedetomidine) GroupII(low dose infusion of dexmedetomidine) Control Intervention1: Dexmedetomidine as Bolus and l

Sponsors

NONE
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of ASA physical status Iâ??II, aged 2â??10 years of either sex with + 20% of ideal body weight, would be enrolled in this prospective, randomized, double blind study.

Exclusion criteria

Exclusion criteria: Patients with history of developmental delay, cardiac disorders, psychological disorders, epilepsy and allergy to study medications would be excluded from the study.

Design outcomes

Primary

MeasureTime frame
To see emergence agitation by using PAEDS scale,pain by using OPS score and sedation by using RSS score.Timepoint: Postoperatively for one hour—

Secondary

MeasureTime frame
DRUG MORE EFFECTIVE FOR PREVENTION OF EMERGENCE AGITATION WITH BOLUS OR LOW DOSE INFUSION OF DEXMEDETOMIDINETimepoint: ONE YEAR—

Countries

India

Contacts

Public ContactVINITA SINGH

KING GEORGES MEDICAL UNIVERSITY LUCKNOW

uzmabegum09@gmail.com8176861027

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026