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Observation of clinical effect of calendula moisturizing repair spray and mask applied to 1064nm fractional picosecond laser postoperative care

Observation of clinical effect of calendula moisturizing repair spray and mask applied to 1064nm fractional picosecond laser postoperative care

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100055009
Enrollment
Unknown
Registered
2021-12-30
Start date
2021-12-24
Completion date
Unknown
Last updated
2023-01-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Experimental group:Use Calendula Moisturizing Repair Spray and Mask After Laser Surgery
Control group:Using a Mask After Laser Surgery

Sponsors

Ninth People's Hospital Affiliated to Shanghai Jiaotong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 65 years, gender is not limited; 2. Good health, no history of serious diseases such as cardiovascular system, digestive system, endocrine system, immune system, nervous system; no history of mental and psychological abnormalities; 3. In line with 1064nm fractional picosecond laser facial treatment indications, such as acne scars, photoaging, enlarged pores, etc.; 4. No skin barrier damage, no obvious telangiectasia, chloasma, etc.; 5. The subjects fully understand the content of the experiment, voluntarily participate in the experiment, and have signed the informed consent; 6. There is no history of skin chemical peeling, other history of photoelectric therapy or participation in other clinical research that affects the observation of this test within 3 months; 7. No history of drug allergy, skin tumor, dermatitis, eczema and other skin diseases; 8. Be able to conduct treatment, data collection, and cooperate with visits according to research requirements.

Exclusion criteria

Exclusion criteria: 1. Those who are known to be allergic to the active ingredients or excipients of the research cosmetics; 2. Those with obvious signs of bacterial, fungal, viral or other pathogen infection on the facial skin, such as: acne, folliculitis, herpes simplex, flat wart, etc.; 3. Those who have a history of herpes simplex in the past; 4. Those who are preparing for pregnancy, pregnancy and lactation; 5. Those who use Chinese herbal medicine, sedatives or other addictive drugs; 6. Alcoholics, mentally ill patients, or unable to cooperate with treatment and research as prescribed by a doctor; 7. Patients with a history of photosensitivity diseases (chronic actinic dermatitis, systemic lupus erythematosus, etc.), skin photosensitivity, porphyrin allergy, porphyria, etc.; 8. Oral or external use of photosensitizing drugs or hormones.

Design outcomes

Primary

MeasureTime frame
Transepidermal water loss;

Secondary

MeasureTime frame
Adverse reaction rate;Patient satisfaction;

Countries

China

Contacts

Public ContactDong Jiying

Ninth People's Hospital Affiliated to Shanghai Jiaotong University School of Medicine

docdongjiying@163.com+86 13917235344

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026