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NB-UVB phototherapy versus excimer laser after minigrafting in vitiligo patients.

NB-UVB phototherapy versus excimer laser after minigrafting in vitiligo patients.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON29475
Enrollment
24
Registered
2006-10-03
Start date
2006-09-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

None listed

Interventions

Minigrafting in two symmetrical vitiligo patches on the trunk or extremties.

Sponsors

none
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Consecutive patients, diagnosed with stable vitiligo vulgaris* with symmetrical vitiligo patches. *Vitiligo vulgaris: a few to many widespread depigmented macules over the entire body, with often a symmetrically distribution pattern. Stable means: no expansion of existing lesions or appearance of new lesions during the previous 6 months, absence of Koebner's phenomenon and a positive minigrafting test; 2. Patients, eligible for minigrafting and NB-UVB/excimer therapy; 3. Adult patients: older than 18 years.

Exclusion criteria

Exclusion criteria: Patients: 1. With a history of hypertrophic scarring and/or keloid; 2. History of allergic/phototoxic reaction (Lidocaine, Tegaderm, Suture strips, sunlight); 3. With a negative minigrafting test; 4. With a personal or a family history of skin cancer (non-melanoma skin cancer: first degree family members, melanoma: any family member); 5. With a personal history of photosensitivity and/or phototoxicity disorders; 6. With skin type I (according to Fitzpatrick classification I-VI); 7. Who are pregnant; 8. Who are taking medications known to cause photosensitivity and/or phototoxicity and chronic or very frequent use of any medication that can influence the UVB response (eg. tetracycline, retinoids, sulfonamids, psoralens, NSAID¡¯s); 9. With other skin diseases that would impair evaluation of repigmentation, such as psoriasis and eczema; 10. Who are not able to have 2 times weekly NB-UVB/Excimer therapy; 11. With local immunosuppressive treatment or 6 weeks prior to enrolment. For these patients a washout period of 6 weekswill be required.

Design outcomes

Primary

MeasureTime frame
Percentage, start and grade of repigmentation.

Secondary

MeasureTime frame
Patient satisfaction.

Contacts

Public ContactM.W. Linthorst Homan

Academic Medical Center (AMC), Department of Dermatology, Netherlands Institute of Pigmentary Disorders Meibergdreef 35

m.w.linthorsthoman@amc.uva.nl+31 (0)20 5666955

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)