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NCT05861063Phase 4
Key facts
Phase 4, randomised trial of dezocine in procedural pain (3 arms), sponsored by Xijing Hospital. Primary endpoints: Visual Analog Score for Pain at 24 hours, Hemodynamic parameters at 24 hours and 2 more. Status: unknown.
Control Group
Placebo (Normal Saline) + Laser
Dezocine Low Dose
Low dose Dezocine + Laser
Dezocine High Dose
High dose Dezocine + Laser
Adult patients aged 18-60 with atrophic acne scars planning to undergo ultra-pulsed CO2 lattice laser therapy. Excludes patients with severe heart, lung, liver, or kidney diseases, psychosis, pregnancy, communication disorders, history of hypertension >160/100mmHg, sleep apnea, increased intracranial pressure, alcoholism, hypotension, hypothyroidism, acute asthma, or epilepsy.
Visual Analog Score for Pain
Hemodynamic parameters
Heart rate (HR)
oxygen saturation (SpO2)
Occurrence of Adverse Reactions
Beyond the preview
Full results, competitive context and analysis are in the Gosset platform.
Available in the Gosset platform where reported.
Available in the Gosset platform where reported.
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