Efficacy and Safety of Lidocaine and Tetracaine Cream for Facial Laser Aesthetics in Chinese Adults
NCT ID: NCT05793892
Last Updated: 2024-11-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE3
286 participants
INTERVENTIONAL
2023-04-06
2023-10-25
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
QUADRUPLE
Study Groups
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Arm A
The order of administration of the test drug in both treatment areas in Arm A is the first, followed by the use of the control drug.
Lidocaine tetracaine cream
The test drug and the control drug will be uniformly spread over the treatment area using a tongue platula to form a thin layer of approximately 1 mm,right then left . The drug remained in the treatment area for 30 minutes (± 2 minutes) .
Arm B
The order of administration in both treatment areas in Arm B was the use of the control drug first, followed by the investigational drug.
Lidocaine tetracaine cream
The test drug and the control drug will be uniformly spread over the treatment area using a tongue platula to form a thin layer of approximately 1 mm,right then left . The drug remained in the treatment area for 30 minutes (± 2 minutes) .
Interventions
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Lidocaine tetracaine cream
The test drug and the control drug will be uniformly spread over the treatment area using a tongue platula to form a thin layer of approximately 1 mm,right then left . The drug remained in the treatment area for 30 minutes (± 2 minutes) .
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* 2、Aged 18-65 years old (including the boundary value), gender is not limited;
* (3) Body mass index (BMI) between 18.5-28.0 kg/m2 (including the boundary value);
* (4) plan to perform facial lattice laser cosmetic;
* (5) The subject can communicate well with the investigator and can complete the study in accordance with the provisions of the study.
Exclusion Criteria
* (2) sensory disturbance, hyperalgesia, migraine, herpes zoster, trigeminal neuralgia and other head and facial pain affect the efficacy evaluation;
* (3) Those who have used any analgesics within 24 hours before surgery;
* (4) Patients with allergic constitution \[to two or with substances (dust, pollen, food, drugs, etc.)\], or known to be allergic to lidocaine, tetracaine or other amide or ester local anesthetics and its excipients or p-aminobenzoic acid (PABA);
* (5) Those who are sensitive to systemic effects of lidocaine and tetracaine (such as acute disease, severe liver disease or pseudocholinesterase deficiency);
18 Years
65 Years
ALL
Yes
Sponsors
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Cutia Therapeutics(Wuxi)Co.,Ltd
INDUSTRY
Responsible Party
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Locations
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Shanghai Ninth People Hospital,Shanghai Jiaotong University School of Medicine
Shanghai, Shanghai Municipality, China
Beijing Hospital
Beijing, , China
Beijing Tsinghua Changgung Hospital
Beijing, , China
Peking University Shougang Hospital
Beijing, , China
Xiangya Hospital Central South University
Changsha, , China
West China School of Medicine West China Hospital of sichuan university
Chendu, , China
Fujian Medical University Union Hospital
Fuzhou, , China
Nanfang Hospital/Guangzhou
Guangzhou, , China
Jiangsu Province Hospital
Nanjing, , China
Union Hospital, Tongji Medical college huazhong university of science and technology
Wuhan, , China
The affiliated hospital of xuzhou medical university
Xuzhou, , China
Countries
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Other Identifiers
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CU-30101-304
Identifier Type: -
Identifier Source: org_study_id
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