Lidocaine co-infusion for prevention of vascular pain induced by crystalloid solution infusion

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR1900023753

Enrollment

Unknown

Registered

2019-06-10

Start date

2019-06-24

Completion date

Unknown

Last updated

2019-06-17

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

Conditions

vascular pain

Interventions

control:normal saline

Experimental group:lidocaine

Eligibility

Sex/Gender

All

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Aged 18-60 years; scheduled elective surgery; patients requiring intravenous crystalloid solution preloading before anesthesia; clear mind; able to communicate effectively.

Exclusion criteria

Exclusion criteria: Failure to establish peripheral vein on dorsum of hand; limb sensorimotor disorder; ASA grade 3-5; unwilling to participate in this study.

Design outcomes

Primary

Measure	Time frame
degree of pain;	—

Countries

China

Contacts

Public ContactSong Zhiping

The First Affiliated Hospital of Nanchang University

pig.12345@163.com+86 15979079071

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026