Effect of lidocaine spray on pain of noninvasive needle puncture in patients at infusion port: a randomized controlled trial

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2300072976

Enrollment

Unknown

Registered

2023-06-29

Start date

2023-01-01

Completion date

Unknown

Last updated

2023-07-02

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

Conditions

Hospitalized patients

Interventions

Control group:water spray

Experimental group:lidocaine spray

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Age = 18 years old; No history of mental illness and normal cognition, with clear language expression; Normal pain response; The skin at the injection site is intact, without damage, redness, or infection

Exclusion criteria

Exclusion criteria: ? Long term use of analgesic drugs; ? Allergic to lidocaine and spray.

Design outcomes

Primary

Measure	Time frame
pain;	—

Secondary

Measure	Time frame
comfort;accept;Puncture success rate;	—

Countries

China

Contacts

Public Contactliqin ye

shanghai general hospital

793512578@qq.com+86 150 0001 5398

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 10, 2026