Back to resultsPulsed Dye Laser and Intense Pulsed Light (IPL) for the Treatment of Telangiectasia and Skin Redness
Primary Purpose
Telangiectasis, Erythema
Status
Unknown status
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Pulsed dye laser
Intense pulsed light
Sponsored by
About this trial
This is an interventional treatment trial for Telangiectasis focused on measuring Telangiectasia, Skin redness
Eligibility Criteria
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
Sites / Locations
- Bispebjerg HospitalRecruiting
Outcomes
Primary Outcome Measures
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00206921
Brief Title
Pulsed Dye Laser and Intense Pulsed Light (IPL) for the Treatment of Telangiectasia and Skin Redness
Official Title
Pulsed Dye Laser and Intense Pulsed Light for the Treatment of Telangiectasia and Skin Redness
Study Type
Interventional
2. Study Status
Record Verification Date
December 2004
Overall Recruitment Status
Unknown status
Study Start Date
February 2005 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
August 2005 (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
Bispebjerg Hospital
4. Oversight
5. Study Description
Brief 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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Telangiectasis, Erythema
Keywords
Telangiectasia, Skin redness
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
Single
Allocation
Randomized
8. Arms, Groups, and Interventions
Intervention Type
Device
Intervention Name(s)
Pulsed dye laser
Intervention Type
Device
Intervention Name(s)
Intense pulsed light
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Merete Hædersdal, MD, PhD, DrMedSci
Phone
+45 35 31 60 02
Email
mhaedersdal@dadlnet.dk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Merete Hædersdal, MD, PhD, DrMedSci
Organizational Affiliation
Bispebjerg Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Bispebjerg Hospital
City
Copenhagen
State/Province
Copenhagen NV
ZIP/Postal Code
2400
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Merete Hædersdal, MD, PhD, DrMedSci
Phone
+4535316002
Email
mhaedersdal@dadlnet.dk
12. IPD Sharing Statement
Learn more about this trial
Pulsed Dye Laser and Intense Pulsed Light (IPL) for the Treatment of Telangiectasia and Skin Redness
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