The Application of Bovine Basic Fibroblast Growth Factor Gel in the Treatment of Sensitive Skin
NCT ID: NCT06516939
Last Updated: 2024-07-24
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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RECRUITING
NA
28 participants
INTERVENTIONAL
2024-06-10
2024-07-18
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
SINGLE_GROUP
TREATMENT
DOUBLE
Study Groups
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The Application of Bovine Basic Fibroblast Growth Factor Gel
bFGF
Half-face randomized control
Bovine Basic Gel
Bovine Basic Gel
Bovine Basic Gel
Interventions
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bFGF
Half-face randomized control
Bovine Basic Gel
Bovine Basic Gel
Eligibility Criteria
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Inclusion Criteria
2. No related skin care products including bovine alkaline fibroblast growth factor were used within 1 month before participating in the experiment, and photoelectric treatment measures were not carried out
3. Physical sunscreen should be strict during enrollment
Exclusion Criteria
2. Have serious heart, liver, kidney, and blood system diseases, and severe immunocompromise
3. Patients with mental illness or cancer
4. Those who have received glucocorticoids, calcineurin inhibitors, topical small molecule drugs, antibiotics or tretinoin within 3 months
5. Those who are allergic to basic fibroblast growth factor gel and its components
6. Acute dermatitis of the face and perifolliculitis
18 Years
60 Years
ALL
No
Sponsors
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Shanghai Dermatology Hospital
OTHER
Responsible Party
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Locations
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Shanghai Skin Disease Hospital
Shanghai, , China
Countries
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Central Contacts
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Facility Contacts
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Haiyan Zhang, MD PhD
Role: primary
Other Identifiers
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2024-06
Identifier Type: -
Identifier Source: org_study_id
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