Effects of intravenous lidocaine administration on postoperative quality of recovery of patients with painless bronchoscopy procedure: a randomized, double-blind and controlled trial.

Effects of Intravenous Infusion of Lidocaine on Postoperative Recovery Quality in Patients After Painless Fiberoptic Bronchoscopy: a Randomized Controlled Double-Blind Study

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR1900025203

Enrollment

Unknown

Registered

2019-08-16

Start date

2019-09-01

Completion date

Unknown

Last updated

2019-08-27

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

Conditions

Quality of Recovery

Interventions

Group C:saline

Group L:Lidocaine

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 100 patients with painless Fiberoptic Bronchoscopy aged 18 to 65 years, American Society of Anesthesiologists (ASA) physical status I or II were recruited from the First Affiliated Hospital of Anhui Medical University.

Exclusion criteria

Exclusion criteria: Those patients will be excluded if they are unwilling to comply with the protocol, or they have renal failure, liver insufficiency, major cardiac arrhythmia, allergy to lidocaine.

Design outcomes

Primary

Measure	Time frame
Quality of Recovery score;	—

Secondary

Measure	Time frame
Anesthesia Time;Surgery Time;Recovery time;Dose of Propofol;Dose of Sufentanil;The satisfaction of patients;	—

Countries

China

Contacts

Public ContactYuanhai Li

The First Affiliated Hospital of Anhui Medical University

yangxiuli2005@163.com+86 13505697561

Outcome results

None listed

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