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prospective trial to validate the efficacy of peripheral nerve blocks in pediatrics after orthopedic surgery to reduce postoperative anxiety after emergence

the relationship between peripheral nerve block for post operative pain control and anxiety after emergence in pediatric orthopedics surgery patients.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0002086
Enrollment
50
Registered
2016-09-30
Start date
2016-07-07
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

None listed

Interventions

Procedure/Surgery : control group: fentanyl 1microgram/kg intravenuos injection before incision. study group: pheripheral nerve block by 0.25&#37
ropivacaine on the operative site after general anesthesia. a doctor works for intervention and another doctor score the patient in postanesthetic care units. therfore, scoring doctor don&#39
t know whether intervention or not.

Sponsors

Chungnam National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: american society of anesthesiologist physical status I-II, aged 2yrs~7yrs patients scheduled for elective orthopedic surgery

Exclusion criteria

Exclusion criteria: Refuse nerve block local infection, amide anesthetics(ropivacaine) hypersensitivity local anesthetics dose exceed permitted capacity by peripheral nerve block due to multiple injury.

Design outcomes

Primary

MeasureTime frame
paed (pediatric agitation and emergence delirium) scale ,postoperatively

Secondary

MeasureTime frame
modified cheops (children's hospital of eastern ontario pain score), postoperatively ;number of pain control drug, postoperative;postoperative time, drug dose, drug type (pain control drug demand) ;checkout time of PACU (postanesthetic care units)

Countries

Korea, Republic of

Contacts

Public ContactBoohwi Hong

Chungnam National University Hospital

koho0127@gmail.com+82-42-280-7840

Outcome results

None listed

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