KTP Laser vs Pulsed Dye Laser for Port-Wine Stains
Primary Purpose
Port-Wine Stain
Status
Recruiting
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
KTP
PDL
Sponsored by
About this trial
This is an interventional treatment trial for Port-Wine Stain
Eligibility Criteria
Inclusion Criteria: Men and women 18 years and older Good general health, no relevant previous diseases Presence of one or more port-wine stains Cognitive ability and willingness to give consent (Informed Consent) Exclusion Criteria: Age < 18 years Pregnant and breastfeeding women Significant open wounds or lesions in the region to be treated Missing consent and/or data protection declarations
Sites / Locations
- Laser Department, University Medical Center Hamburg-EppendorfRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Potassium Titanyle Phosphate (KTP) Laser
Pulsed Dye Laser
Arm Description
split-side, 1 - 5 sessions at intervals of 6 - 8 weeks
split-side, 1 - 5 sessions at intervals of 6 - 8 weeks
Outcomes
Primary Outcome Measures
Erythema
assessment scale 1 - 7 (normal skin - dark purple) evaluated by physician and blinded investigator
area reduction
measurement using photo documentation
Secondary Outcome Measures
patient satisfaction
assessment scale 1 - 6 (very - not at all) evaluated by subjects
Full Information
NCT ID
NCT05771311
First Posted
March 5, 2023
Last Updated
March 5, 2023
Sponsor
Universitätsklinikum Hamburg-Eppendorf
1. Study Identification
Unique Protocol Identification Number
NCT05771311
Brief Title
KTP Laser vs Pulsed Dye Laser for Port-Wine Stains
Official Title
Potassium Tetanyl Phosphate Laser vs Pulsed Dye Laser for Treating Port-Wine Stains - A Prospective, Split-Side Study
Study Type
Interventional
2. Study Status
Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 1, 2023 (Actual)
Primary Completion Date
May 1, 2023 (Anticipated)
Study Completion Date
August 1, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Universitätsklinikum Hamburg-Eppendorf
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
To compare the efficacy and safety of 532nm KTP laser and 585 nm pulsed dye laser for treating port-wine stains.
Detailed Description
Nevus flammeus is a vascular, primarily capillary malformation visible from birth on. In rare cases, it may also affect venous and/or arterial vascular systems of the skin or other organs [1]. It occurs in 0.3%-0.5% of the population [1], i.e. in about 3-4 out of 1000 newborns, and is thus the most frequent vascular malformation in children. The cause is a permanent dilatation of the capillary vessels, which is caused by a lack of sympathetic nerve fibers or a lower density of the same.
First-line therapy of port-wine stains consists of laser treatment with the long-pulsed dye laser [2] with a wavelength of 595nm. Treatment must be performed at least 10 times at intervals of about 8 weeks and leads to lightening and reduction of lesions. In recent years, problems have often arisen in care of port-wine stain patients because dye lasers often failed due to the instability of technology, resulting in treatment delays. Novel long-pulsed KTP lasers may be a sufficient alternative to pulsed dye lasers in treatment of port-wine stains.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Port-Wine Stain
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Potassium Titanyle Phosphate (KTP) Laser
Arm Type
Active Comparator
Arm Description
split-side, 1 - 5 sessions at intervals of 6 - 8 weeks
Arm Title
Pulsed Dye Laser
Arm Type
Active Comparator
Arm Description
split-side, 1 - 5 sessions at intervals of 6 - 8 weeks
Intervention Type
Device
Intervention Name(s)
KTP
Intervention Description
split-side, 1 -5 sessions at intervals of 6 - 8 weeks
Intervention Type
Device
Intervention Name(s)
PDL
Intervention Description
split-side, 1 -5 sessions at intervals of 6 - 8 weeks
Primary Outcome Measure Information:
Title
Erythema
Description
assessment scale 1 - 7 (normal skin - dark purple) evaluated by physician and blinded investigator
Time Frame
at follow-up visit 6 weeks after last treatment session
Title
area reduction
Description
measurement using photo documentation
Time Frame
at follow-up visit 6 weeks after last treatment session
Secondary Outcome Measure Information:
Title
patient satisfaction
Description
assessment scale 1 - 6 (very - not at all) evaluated by subjects
Time Frame
at follow-up visit 6 weeks after last treatment session
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Men and women 18 years and older
Good general health, no relevant previous diseases
Presence of one or more port-wine stains
Cognitive ability and willingness to give consent (Informed Consent)
Exclusion Criteria:
Age < 18 years
Pregnant and breastfeeding women
Significant open wounds or lesions in the region to be treated
Missing consent and/or data protection declarations
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
L Nguyen, MD
Phone
+49 (0)40 7410-0
Email
l.nguyen@uke.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
L Nguyen
Organizational Affiliation
Universitätsklinikum Hamburg-Eppendorf
Official's Role
Principal Investigator
Facility Information:
Facility Name
Laser Department, University Medical Center Hamburg-Eppendorf
City
Hamburg
ZIP/Postal Code
20246
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
L Nguyen, MD
Phone
040 7410 0
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
22305042
Citation
Chen JK, Ghasri P, Aguilar G, van Drooge AM, Wolkerstorfer A, Kelly KM, Heger M. An overview of clinical and experimental treatment modalities for port wine stains. J Am Acad Dermatol. 2012 Aug;67(2):289-304. doi: 10.1016/j.jaad.2011.11.938. Epub 2012 Feb 3.
Results Reference
background
PubMed Identifier
29141064
Citation
Updyke KM, Khachemoune A. Port-Wine Stains: A Focused Review on Their Management. J Drugs Dermatol. 2017 Nov 1;16(11):1145-1151.
Results Reference
background
Learn more about this trial
KTP Laser vs Pulsed Dye Laser for Port-Wine Stains
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