NCT00206921

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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Timeline
Completed

Started Feb 2005

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2005

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2005

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

September 13, 2005

Completed
8 days until next milestone

First Posted

Study publicly available on registry

September 21, 2005

Completed
Last Updated

July 25, 2007

Status Verified

December 1, 2004

First QC Date

September 13, 2005

Last Update Submit

July 23, 2007

Conditions

TelangiectasisErythema

Keywords

TelangiectasiaSkin redness

Interventions

Pulsed dye laserDEVICE
Intense pulsed lightDEVICE

Eligibility Criteria

Age18 Years+
Sexall
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • years or older
  • Skin types I, II, III
  • No previous laser or IPL treatment for the condition

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Bispebjerg Hospital

Copenhagen, Copenhagen NV, 2400, Denmark

RECRUITING

MeSH Terms

Conditions

TelangiectasisErythema

Interventions

Lasers, DyeIntense Pulsed Light Therapy

Condition Hierarchy (Ancestors)

Vascular DiseasesCardiovascular DiseasesSkin DiseasesSkin and Connective Tissue DiseasesSkin ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

LasersOptical DevicesEquipment and SuppliesRadiation Equipment and SuppliesPhototherapyTherapeutics

Study Officials

  • Merete Hædersdal, MD, PhD, DrMedSci

    Bispebjerg Hospital

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Merete Hædersdal, MD, PhD, DrMedSci

CONTACT

+45 35 31 60 02mhaedersdal@dadlnet.dk

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER

Study Record Dates

First Submitted

September 13, 2005

First Posted

September 21, 2005

Study Start

February 1, 2005

Study Completion

August 1, 2005

Last Updated

July 25, 2007

Record last verified: 2004-12

Locations

DK(1)