Intravenous Lidocaine Pretreatment with Drooping Limb versus Tourniquet for Reducing Microemulsion Propofol Induced Pain: A Randomized, Double-blind Trial

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-ICR-14005613

Enrollment

Unknown

Registered

2014-12-01

Start date

2014-12-02

Completion date

Unknown

Last updated

2017-04-18

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

Conditions

Stroke

Interventions

drooping limb group:Injection with drooping limb

Tourniquet group:Injection with tourniquet for venous occlusion

Classical injection group :Injection without any special manipulation

Eligibility

Sex/Gender

All

Age

20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients with ASA physical status I or II, aged 20 to 60 years and scheduled for elective surgery under general anesthesia were recruited.

Exclusion criteria

Exclusion criteria: Patients were excluded if they had a known hypersensitivity to lidocaine or propofol; communication difficulty; habituation to analgesics, sedatives or anti-anxiety drugs; and a renal, hepatic, cardiac, or neurologic problem, which may affect the study results. Also excluded were those with a Body Mass Index more than 25 or less than 20 in male, and more than 24 or less than 19 in female.

Design outcomes

Primary

Measure	Time frame
pain score;	—

Countries

China

Contacts

Public ContactBing Zhang

zhang_bing08@126.com+86 13796620602

Outcome results

None listed

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