Skin changes before and after CO₂ laser or Thermage treatment
Official title: Pre- and Post-procedure Skin Knowledge Study
Run by ChinaNorm · NCT07895303 · Data updated 2026-11-12
This study tests how skin signs and feel change before and after CO₂ fractional laser or Thermage treatment in Asian women.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 30 Years to 59 Years |
| Sex | Women only |
| Enrollment | 60 (estimated) |
| Sponsor | ChinaNorm Industry-sponsored |
| Locations | 1 site (Shanghai, Shanghai Municipality) |
| Status | Recruiting |
| Started | October 9, 2026 |
| Main results expected | June 11, 2027 |
| Study ends | June 11, 2027 |
| Registry record updated | October 26, 2026 |
| Trial ID | NCT07895303 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are Asian women aged 30–59 in good health with dermatologically confirmed, healthy facial skin and specific baseline aging characteristics.
✕Probably not a fit
Patients with skin conditions outside the eligibility criteria or those not meeting baseline facial criteria may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The study compares skin signs, physiology, and subjective well-being before and after two aesthetic procedures. It uses blinded assessors for treatment group while participants know their treatment due to visible effects. Participants will use only neutral skincare products for two weeks around the procedures. The goal is to explore correlations between skin parameters and to identify the best time to start skincare after treatment.
Why it matters
Potential benefit: If successful, the study could guide post-treatment skincare timing to optimize recovery and satisfaction.
How similar studies have gone: Previous work in skin rejuvenation procedures has shown measurable skin changes, but this exact comparative, timing-focused approach is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * 1\) Asian women, with age range from 30 to 59 years old; * 2\) Be in general good health and good mental state; * 3\) Presenting healthy skin as determined by Dermatologist; * 4\) All Fitzpatrick skin types; * 5\) All skin types on face (dry, normal, oily and combination) by subjects' self-perceived, with sensitive skin status confirmed and documented by a dermatologist; * 6\) Facial skin exhibits specific characteristics (the mean baseline needs to be the same for 2 groups for all those parameters, before the pre-treatment phase T-2w) which require dermatological evaluation, detailed as follows: Crow's feet wrinkles: grade: 3≤ grade ≤5 (SKIN AGING ATLAS, page 40 to 41) Underneath eyes wrinkles: 3≤ grade ≤6 (SKIN AGING ATLAS, page 46 to 47) Ptosis of the lower part of the face: 1≤ grade ≤3 (SKIN AGING ATLAS, page 66 to 67) Lack of firmness: 3≤ grade ≤6 (9-point scale, 0 is the worst, 9 is the best) Pigmentary spots: 3≤ grade ≤5 (SKIN AGING ATLAS, page 79 to 81) (only for CO2 fractional laser Group) * 7\) Willing to participate in one session of aesthetic procedure, either Fractional Ultrapulse CO₂-laser or Thermage procedure, after a 2-week wash-out period, followed by a 10-day self-recovery observation period. * 8\) Aware and willing to accept that after a 10-day healing period, if the skin is not "ready" for the application of cosmetic products as determined by a dermatologist, they will be required to withdraw from the study; * 9\) Have clean testing area (face): free of make-up on face, free of skin care products (lotions, sunscreens), make-up, perfumes, or other topical products on the visit day; * 10\) Not currently be participating and will not participate in any other study involving the test area (face) for the duration of the study; * 11\) Not have participated in any other study involving the test area (face) in the past 1 month; * 12\) Be willing to read, understand and able to sign the Informed Consent Form \& Photo Release Form; * 13\) Be willing to comply with all study protocol requirements. Exclusion Criteria: * 1\) Intending to get pregnant, be pregnant, be lactating, be within 6 months of delivery or be unwilling to take necessary precautions to avoid a pregnancy; * 2\) Have any skin problems to impact clinical assessment, such as large areas of acne, scars, and open wounds, etc.; * 3\) Having used antihistamine drugs in the past 1 week and one month after the treatment or immunosuppressants in the past 1 month; * 4\) Take anti-allergic drug/injections in the past 1 month; * 5\) Presently have allergies, allergic dermatitis or skin disease; * 6\) Have sensitivity or even allergy to topical products, ingredients or fragranced products; * 7\) Having a history of allergies, including but not limited to allergies to certain ingredients in cosmetics. * 8\) Have history of suffering from skin diseases (such as psoriasis, eczema, psoriasis, skin cancer, etc.); * 9\) Have used any anti-inflammatory treatment on the test area within 2 months prior to this study starting date; * 10\) Has a chronic medical condition that may interfere with testing (e.g., asthma, insulin-dependent diabetes, lupus, rheumatoid arthritis or other immune/auto-immune diseases); * 11\) Have received cosmetic medical procedures on the face (such as injectable anti-wrinkle products, cosmetic surgery, tattoo removal, home light facial procedures or home use medical devices, etc.) in the past 6 month; For Thermage group: priority screening for fillers, thread lifts, and metallic implants in the treatment area; For CO2 fractional laser Group: priority screening for laser treatments, peeling procedures, isotretinoin treatmentrecently and risk of herpes simplex virus (HSV) reactivation and post-inflammatory hyperpigmentation (PIH); * 12\) Have excessive sun exposure or ultraviolet light in the past 1 month; * 13\) Have applied Alpha hydroxyl acid, ortho-hydroxybenzoic acid, hydroquinone in the past 3 months; or used prescriptions (such as antibiotic, retinoids, alpha hydroxyl acid and steroid), oral contraceptives (such as Diane 35®,Jasmine®,Holgyeme®,Syndi 35®,Regulon®); * 14\) Avoid providing emergency contact; * 15\) Subjects that are not compliant to the selection criteria or not proper for participation as determined by Principal Investigator; * 16\) An employee of the cosmetic companies or Shanghai China-Norm Quality Technical Service Co., Ltd.
Where it's running
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Shanghai China-norm Quality Technical Service Co., Ltd., Shanghai, Shanghai 200072, Shanghai,
Shanghai, Shanghai Municipality, China Recruiting
Study contacts
- Principal investigator: Yanwen Jiang — Shanghai China-norm Quality Technical Service Co., Ltd.
- Study coordinator: Yanwen Jiang
- Email: jiangyanwen@china-norm.com
- Phone: 13501700841
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.