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Scalp Nerve Block on Emergence Agitation

A

Ajou University School of Medicine

Status and phase

Completed
Phase 4

Conditions

Agitation

Treatments

Drug: Sevoflurane
Drug: Remifentanil
Drug: Ropivacaine

Study type

Interventional

Funder types

Other

Identifiers

NCT02428283
AJIRB-MED-CT4-14-422

Details and patient eligibility

About

Emergence agitation is a common problem in children during recovery from sevoflurane anesthesia. Pain is considered as a cause of postoperative emergence agitation and compounding factor of agitation assessment in children. The purpose of this study was to investigate the effect of scalp nerve block on the emergence agitation in children undergoing nevus surgery during sevoflurane anesthesia.

Full description

Forty-four children, 1-7 years old, undergoing nevus surgery on head were enrolled. Anesthesia was induced with thiopental sodium and rocuronium, and maintained with sevoflurane. Patients were randomly assigned two groups: the control group received IV remifentanil 1 μg/kg, and the block group received scalp nerve block with 0.25% ropivacaine 2-3 ml. Time to tracheal extubation, recovery time, hemodynamic change, FLACC score, and Watcha behavior scale for emergence agitation were assessed.

Enrollment

44 patients

Sex

All

Ages

1 to 7 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ASA I-II patients undergoing general anesthesia for nevus surgery

Exclusion criteria

  • developmental disorder
  • neurologic disorder
  • coaguloparthy
  • allergy to local anesthetics

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

44 participants in 2 patient groups

Nerve block
Experimental group
Description:
Scalp nerve block was performed with 0.25% ropivacaine.
Treatment:
Drug: Ropivacaine
Drug: Sevoflurane
Control
Active Comparator group
Description:
Remifentanil was administered intravenously.
Treatment:
Drug: Remifentanil
Drug: Sevoflurane

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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