Comprehensive evaluation of postoperative outcome and postoperative agitation of children with upper limb fracture treated with different anesthetics

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2200057094

Enrollment

Unknown

Registered

2022-02-28

Start date

2022-03-01

Completion date

Unknown

Last updated

2023-09-26

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

Conditions

Unilateral supracondylar fracture of humerus

Interventions

Control group:None

Ropivacaine group:Ropivacaine nerve block

Mepivacaine group:Mepivacaine nerve block

Eligibility

Sex/Gender

All

Age

3 Years to 10 Years

Inclusion criteria

Inclusion criteria: 1. Three to ten years old children with unilateral supracondylar fracture of humerus, without other combined injuries; 2. ASA grade I-II.

Exclusion criteria

Exclusion criteria: 1. Local anesthesia drug allergy history; 2. Respiratory inflammation attack stage; 3. Congenital disease history; 4. Refused to participate in the experiment.

Design outcomes

Primary

Measure	Time frame
Agitation score;	—

Secondary

Measure	Time frame
VASscore;	—

Countries

China

Contacts

Public ContactQiujun Wang

The Third Hospital of Hebei Medical University

13933178001@163.com+86 18533112929

Outcome results

None listed

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