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Dexmedetomidine decreases the required concentration of bupivacaine for ultrasound-guided transversus abdominis plane block in pediatric patients

Dexmedetomidine decreases the required concentration of bupivacaine for ultrasound-guided transversus abdominis plane block in pediatric patients: a randomized double-blind up-down dose-finding study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR201502001009132
Enrollment
60
Registered
2015-01-24
Start date
2015-03-01
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

Surgery Paediatrics ultrasound-guided transversus abdominis plane block in pediatric patients Anaesthesia

Interventions

Group BD (Bupivacaine plus 2µg/kg dexmedetomidine).
GroupB (TAP Bupivacaine)

Sponsors

:Department of Anaesthesia and Surgical Intensive Care
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: patients aged between 1-6years ASA I &II undergoing hernia repair or hydrocelectomy

Exclusion criteria

Exclusion criteria: local infection of the abdominal wall allergic to amide local anesthetics blood clotting disorders neurological, neuromuscular or psychiatric disorders severe renal, hepatic, respiratory, or cardiac diseases

Design outcomes

Primary

MeasureTime frame
The primary endpoint of the study is the minimum local anesthetic concentration (MLAC)

Secondary

MeasureTime frame
pain score measured by FLACC pain score;postoperative sedation

Countries

Egypt

Contacts

Public Contactdoaa abou alia

Assistant Professor Department of Anaesthesia and Surgical Intensive Care, Faculty of Medicine

daboalia@yahoo.com01227392473

Outcome results

None listed

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