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Clinical study of intravenous lidocaine to improve the quality of recovery in patients with obstructive sleep apnea syndrome

Clinical study of intravenous lidocaine to improve the quality of recovery in patients with obstructive sleep apnea syndrome

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400085088
Enrollment
Unknown
Registered
2024-05-30
Start date
2024-05-30
Completion date
Unknown
Last updated
2024-06-03

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

Conditions

Obstructive sleep apnea syndrome

Interventions

lidocaine group:The patient was given lidocaine 1.5 mg/kg for more than 5 minutes and continued to pump lidocaine 2 mg/(kg·h) until the end of the operation. Lidocaine 2mg/(kg·h) was continuously pump
Control group:The patient is given an equal dose of normal saline for more than 5 minutes and continues to pump normal saline until the end of the operation. Postoperative continuous pumping of the sa

Sponsors

Yichang Central People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18-65 years old; 2. ASA grade I~II; 3. The estimated anesthesia operation time= 120min; 4. The patient or the legal client signs the informed consent form.

Exclusion criteria

Exclusion criteria: hypersensitivity to local anesthetics; long-term use of analgesics or cortisols; bradycardia; uncontrolled hypertension, pronounced heart, kidney or liver disease; Endocrine and metabolic diseases; Neurological disorders; Mental or neurological disorders; History of alcoholism.

Design outcomes

Primary

MeasureTime frame
QoR-40;VAS pain score within 48 hours postoperatively;Incidence of postoperative PONV;

Secondary

MeasureTime frame
Intraoperative vasoactive drug use;Total salvage analgesic consumption (mg);Time for extubation;

Countries

China

Contacts

Public ContactGong Yuan

Yichang Central People's Hospital

gy-yc@163.com+86 139 8674 6821

Outcome results

None listed

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