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630nm red light enhanced photodynamic therapy for port-wine stain: a single center, prospective, self controlled study

630nm red light enhanced photodynamic therapy for port-wine stain: a single center, prospective, self controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200065609
Enrollment
Unknown
Registered
2022-11-09
Start date
2023-01-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

port wine stain

Interventions

Control group:532nm light
Intervention Group:532nm + 630nm light

Sponsors

Department of Plastic and Reconstructive Surgery, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University, School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients who meet the port-wine stain diagnostic criteria of the Guidelines for the Diagnosis and Treatment of hemangioma and vascular malformation (2019 edition); 2. Aged between 14 and 65; 3. Simple PWS and related syndromes include SW syndrome (SWS), Phakomatosis pigmentovascularis (PPV), etc. The erythema is required to be relatively isolated from other lesions of the syndrome, that is, there is no other related dermatological changes in the erythema site, such as dermal melanocytosis, etc.; 4. No scar was left after receiving other treatment for more than 3 months; 5. After fully understanding the treatment plan and risks, I or my guardian voluntarily signed the informed consent, willing to accept the clinical trial and cooperate with follow-up.

Exclusion criteria

Exclusion criteria: 1. Patients with original infection, eczema, ulcer and other lesions that may affect the therapeutic effect and with other pigmented diseases such as nevus ota; 2. The patient has a history of epileptic seizures in the last six months or the condition is not controlled; 3. Allergic to porphyrins and analogs, allergic constitution; 4. There is a scar constitution; 5. A history of sun exposure in the last 3 months; 6. Patients with ECG abnormalities, organic heart disease, abnormal liver function, pregnant women or women with pregnancy plans, and other potential diseases that may affect treatment; 7. Is participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
visual analogue scale;

Countries

China

Contacts

Public ContactGang Ma

Shanghai Ninth People's Hospital, Shanghai Jiao Tong University, School of Medicine

docmagang@126.com+86 13761130439

Outcome results

None listed

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