Study of lidocaine to relieve the pain of intravenous cannulation in children

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000032426

Enrollment

Unknown

Registered

2020-04-27

Start date

2020-05-01

Completion date

Unknown

Last updated

2020-05-04

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

Conditions

pain

Interventions

experimental group:Intravenous cannulation was performed after 30 minutes of local anesthesia with lidocaine cream

control group:Intravenous cannulation directly

Eligibility

Sex/Gender

All

Age

3 Years to 12 Years

Inclusion criteria

Inclusion criteria: Children requiring ambulatory surgery and requiring venipuncture; Children and their parents are willing to participate with informed consent.

Exclusion criteria

Exclusion criteria: Children with mental illness, delirium, unable to clearly express their inner feelings;

Design outcomes

Secondary

Measure	Time frame
Success rate of puncture;	—

Primary

Measure	Time frame
pain score;	—

Countries

China

Contacts

Public ContactYaojun Suo

Children's Hospital, School of Medicine, Zhejiang University

suoyaojun1985@126.com+86 13989842130

Outcome results

None listed

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