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Intense Pulsed Light Therapy for Hidrosadenitis Suppurativa

The Effect of Intense Pulsed Light Assisted Hair Removal Therapy on Mild and Moderate Cases of Hidrosadenitis Suppurativa

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03203122
Enrollment
20
Registered
2017-06-29
Start date
2017-08-07
Completion date
2019-08-01
Last updated
2017-06-29

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

Conditions

Acne Inversa, Hidradenitis Suppurativa

Brief summary

6 monthly treatments with IPL laser in patients with Hidradenitis Suppurativa. The effect in measured on several severity scores.

Detailed description

Patient suffering from bilateral HS in the axilla or groin area are threated with IPL laser monthly for 6 months. Patients are randomized to treatment in either left or right side, the other side works as control. No sham treatment, but observers are blinded.

Interventions

OTHERIPL laser

IPL laser monthly. Vertical and horizontal treatment, one pass over. Settings according to fitzpatrick skin type

OTHERNo sham treatment

The treatment is slightly painful, and noisy. Sham treatment impossible

Sponsors

Zealand University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Masking description

Outcome assesor and primary invstigator are blinded and not present at treatments.

Intervention model description

Patients are randomized to treatment in either left or right side, using the other side as control.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Bilateral HS in the axilla or groin area * Fitzpatrick skin type I-II

Exclusion criteria

* Pregnant * Unable to understand or communicate with study personnel

Design outcomes

Primary

MeasureTime frameDescription
HiScoreAfter 6 treatments i.e. 6 months50 % reduction in abcesses and draining fistual

Secondary

MeasureTime frameDescription
Sartorius scoreafter 6 treatments i.e. 6 monthsHS severity score
Physician global assesmentafter 6 treatments i.e. 6 monthsHS severity score

Countries

Denmark

Contacts

Primary ContactPeter Riis, MD
pmik@regionsjaelland.dk47322672
Backup ContactGregor Jemec, DMSc
gbj@regíonsjaelland.dk

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026