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Pre-emptive Topical Lidocaine 5% Plaster for Prevention of Post-craniotomy Pain — EASY  

Postoperative Pain Clinical Trial

Official title:
Pre-emptive Topical Lidocaine 5% Plaster for Prevention of Post-craniotomy Pain : a Protocol for a Randomized, Triple Blind, Placebo-controlled Trail

Clinical Trial Summary

Postcraniotomy pain remains a common phenomenon in the neurosurgery field. Managements for postcraniotomy pain are to be standardised and optimized. In the proposed study, the investigators aim to provide a novel regional non-invasive prophylactic strategy for postcraniotomy pain by utilizing Lidocaine 5% plaster.

Clinical Trial Description

Postcraniotomy pain remains a common phenomenon in the neurosurgery field. Insufficient control of postcraniotomy pain may lead to unexpected clinical outcomes. The current management for postcraniotomy pain mainly involves systemic intravenous or oral medication and regional anaesthetic injection. The investigators intend to compare pre-emptive lidocaine 5% plaster incision covering to a placebo for prophylaxis of postcraniotomy pain. In the proposed study, the effectiveness and safety of lidocaine 5% plaster for postcraniotomy pain control will be examined compared with those of placebo. The investigators aim to provide a novel regional non-invasive prophylactic strategy for postcraniotomy pain. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04169854
Study type Interventional
Source Beijing Tiantan Hospital
Contact Fang Luo, MD
Phone +8613611326978
Email 13611326978@163.com
Status Recruiting
Phase Phase 3
Start date October 15, 2020
Completion date January 2023
View Details
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