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Facial Pores Using Intense Pulsed Light Treatments- a prospective split-face comparison

Facial Pores Using Intense Pulsed Light Treatments- a prospective split-face comparison

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800016757
Enrollment
Unknown
Registered
2018-06-21
Start date
2017-06-01
Completion date
Unknown
Last updated
2018-06-25

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

Conditions

facial pores

Interventions

split-face comparison:IPL

Sponsors

Shanghai 9th People's Hospital Shanghai Jiao tong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1) Aged 18-65 years; 2) healthy patient; 3) Having not accepted any laser or injection treatment in at least 6 months; 4) Having not accepted any oral drugs which will affect blood clotting; 5) Ability and willingness to sign an inform consent form after fully understanding the therapeutic and follow-up strategies.

Exclusion criteria

Exclusion criteria: 1) Insufficient pulmonary functions and hepatorenal functions; 2) Patients with fever or WBC less than 2500 / cubic millimeter; 3) The combined use of other drugs which will affect blood clotting; 4) Serious underlying systemic disease requiring treatment until illness either completes therapy or achieves clinical stablility on therapy for at least 6 months before enrolled the study. The systemic diseases include insufficient pulmonary functions(COPD, pneumonia, pulmonary fibrosis and asthma), insufficient cardiac and hepatorenal functions, infection , hemorrhagic tendency, immunologic disease(SLE, urticaria, HIV); 5) Patient who had accepted any laser or injection treatment in 6 months. The termination criteria to a subject: 1) The four times 1565nm FNAL treatment is finished; 2) The subject requests to terminate treatments; 3) Serious major complications classified by the SIR occurs; 4) The subject becomes pregnant.

Design outcomes

Primary

MeasureTime frame
efficacy;

Countries

China

Contacts

Public ContactWenhsin Yu

Shanghai 9th People's Hospital Shanghai Jiao tong University, School of Medicine

860382817@qq.com+86 15618690545

Outcome results

None listed

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