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Clinical comparative study of CO2 lattice laser and radiofrequency micro needle in the treatment of acne scar

Clinical comparative study of CO2 lattice laser and radiofrequency micro needle in the treatment of acne scar

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100047207
Enrollment
Unknown
Registered
2021-06-10
Start date
2021-07-01
Completion date
Unknown
Last updated
2022-01-24

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

Conditions

Acne scars

Interventions

Experimental group1:Radiofrequency microneedle
Experimental group2:CO2 lattice laser

Sponsors

Shanghai Dermatology Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 50 years (gender unlimited); 2. Atrophic scar after acne; 3. Acne activity; 4. Bilateral symmetry of acne scar; 5. No signs of infection such as ulcers, pus and exudation on the face; 6. The function of heart, lung, liver and kidney is normal; Can not have more than 2 kinds of heart, lung, liver, kidney function complications at the same time; 7. If there is diabetes, blood sugar control is normal; 8. Coagulation function is normal; 9. Stop taking isoretinoic acid capsules for at least 3 months; 10. Written informed consent signed by the patient or his legal agent; 11. Be able to follow up the research or follow-up process; Be able to observe adverse events and curative effect in cooperation.

Exclusion criteria

Exclusion criteria: 1. Active acne, the treatment site has a large number of pustules, cysts or nodules; 2. Fever (body temperature above 37.5 degree) or active infection with obvious influence on clinical trial; 3. There were skin tumors at the treatment site; 4. Scar constitution; 5. There was a history of sun exposure in recent one month; 6. Injection history of fillers in recent two weeks; 7. Grinding history in recent half a year; 8. Patients with malignant tumors of systemic organs and blood system and malignant tumors; 9. There was a history of HIV infection or HIV antibody positive, and there was a history of HSV attack in the treatment site in recent three months; 10. Low immune function and systemic failure; Patients with severe heart, liver, lung, kidney and other important organ diseases are not suitable for clinical trials, such as renal insufficiency requiring dialysis or kidney transplantation; 11, diabetic blood glucose control is bad (fasting blood glucose > 7.0mmol/L, postprandial 2 hour blood sugar > 11.1mmol/L, glycosylated hemoglobin A1C >6.5%); 12. Hematological diseases, including hematological tumors, coagulation disorders, hematopoietic dysfunction; 13. Addiction to drugs, tobacco and alcohol; 14. Have a clear history of mental illness; 15. Participated in the clinical study of any research drug within 1 month (or 5 half lives of the test drug) before enrollment; 16. Pregnant or lactating women; 17. Taking glucocorticoids or other immunosuppressants, anticoagulants, or suffering from autoimmune diseases.

Design outcomes

Primary

MeasureTime frame
Acne scar weight score;

Secondary

MeasureTime frame
Dermatological Quality of Life Scale;

Countries

China

Contacts

Public ContactLi Wei

Shanghai Dermatology Hospital

liwei19860603@163.com+86 18017336477

Outcome results

None listed

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