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Effect of intraoperative intravenous lidocaine infusion on rebound pain after brachial plexus block: A Prospective, Double-Blind, Randomized Controlled Trial

Effect of intraoperative continuous intravenous lidocaine infusion on rebound pain after brachial plexus block

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086229
Enrollment
Unknown
Registered
2024-06-27
Start date
2024-07-01
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

Rebound pain after peripheral nerve block

Interventions

lidocaine group :After the nerve block is administered, receive a continuous intravenous infusion of lidocaine at 2 mg/kg/h.
placebo group:After the nerve block is administered, intravenous injection of physiological saline at an equal rate

Sponsors

Central Hospital of Dalian University of Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.Patients between 18 and 70 yr of age.2.ASA I–III.3.Patients with an upper limb fracture undergo elective surgery under brachial plexus block anesthesia.

Exclusion criteria

Exclusion criteria: 1.refused to participate in research; 2.allergy to lidocaine and ropivacaine 3.coagulation disorders, neuropathic and psychiatric disorders, diaphragmatic paralysis,severe cardiopulmonary disease,cardiac conduction block, pregnancy,severe obesity (body mass index>35 kg/m2) 4.systemic steroid use,any chronic pain and opioids abuse 5.an inability to understand pain scoring or the instructions forintravenous patient-controlled analgesia (PCA);6. a failed brachial plexus block; 7.patients with any residual numbness after 24 hours and with definite peripheral nerve injury,patients do not receive a single injection of nerve block.

Design outcomes

Primary

MeasureTime frame
The incidence of rebound pain;

Secondary

MeasureTime frame
The severity of rebound pain score, the onset and duration of rebound pain;PNB effective analgesic time;Consumption of additional opioid drugs (converted to morphine equivalent if different types);Sleep disorders and possible complications;Overall patient satisfaction with pain control;Has the patient experienced severe pain and/or sleep disorders after discharge, and will they choose nerve block again in the future;

Countries

China

Contacts

Public ContactLi Wang

Central Hospital of Dalian University of Technology (Dalian Central Hospital)

shelly19850124@163.com+86 199 6931 3681

Outcome results

None listed

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