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Phase 1/2 clinical trial of a sustained- release lidocaine sheet for postoperative pai

Phase 1
Conditions
the mandibular horizontal impacted wisdom tooth
Registration Number
JPRN-UMIN000011945
Lead Sponsor
Department Of Anesthesiology Gunma University graduate School of Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
100
Inclusion Criteria

Not provided

Exclusion Criteria

1)A person taking a drug (e.g. antipsychotic, NSAIDs, and opioid) considered to participate in pain relief or judged that the influence is left even if canceled 2)A patient whose surgical site infects remarkably 3)A patient who has an allergy to Lidocaine, an amide type local anaesthetic agent, Celecoxib, a sulfonamide, Acetaminophen 4)A patient with a serious disturbance of conduction system (e.g. complete atrioventricular block) 5)A patient with peptic ulcer or asthma 6)A patient who has disturbance of consciousness or not able to communicate enough to evaluate correctly 7)A patient who is judged unsuitable for this trial by attending doctor

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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