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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00206921
Other study ID # KF-01-236/04
Secondary ID
Status Recruiting
Phase N/A
First received September 13, 2005
Last updated July 23, 2007
Start date February 2005
Est. completion date August 2005

Study information

Verified date December 2004
Source Bispebjerg Hospital
Contact Merete Hædersdal, MD, PhD, DrMedSci
Phone +45 35 31 60 02
Email mhaedersdal@dadlnet.dk
Is FDA regulated No
Health authority Denmark: Ministry of Health
Study type Interventional

Clinical Trial Summary

The purpose of the study is to compare efficacy and adverse effects of pulsed dye laser and intense pulsed light in patients with skin telangiectasia and redness.


Recruitment information / eligibility

Status Recruiting
Enrollment 0
Est. completion date August 2005
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- 18 years or older

- Skin types I, II, III

- No previous laser or IPL treatment for the condition

Exclusion Criteria:

- Younger than 18 years old

- Skin types IV, V, or VI

- Pregnant or lactating women

- Previous laser or IPL treatment for the condition

- Recent exposure to sun or sun-beds

- Treatment with oral retinoid within 6 months

- Tendency to produce hypertrophic scars or keloids

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Device:
Pulsed dye laser

Intense pulsed light


Locations

Country Name City State
Denmark Bispebjerg Hospital Copenhagen Copenhagen NV

Sponsors (1)

Lead Sponsor Collaborator
Bispebjerg Hospital

Country where clinical trial is conducted

Denmark, 

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