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NCT00791908 · ClinicalTrials.gov registry record · NA
Comparison of Electrodessication, Potassium Titanyl Phosphate (KTP) Laser and Pulsed Dye Laser for Treatment of Cherry Angiomata
A NA study of Cherry Angioma, sponsored by Northwestern University.
- Completed
- Registry status
- NA
- Development phase
- 15
- Enrollment target
- 1
- Study location
NCT00791908 is a NA study of Cherry Angioma that has completed, run by Northwestern University. The registered enrollment target is 15 participants. The trial reports 1 study location across 1 state.
The verdict
NCT00791908, a NA study of Cherry Angioma, has completed, sponsored by Northwestern University.
- COMPLETED
- Registry status
- NA
- Development phase
- 15 participants
- Enrollment target
- 1
- Study location
Study Summary
The primary objective of this study is to determine whether laser treatments over 6 weeks using the pulsed dye laser system or the potassium titanyl phosphate (KTP) laser are effective in patients with cherry angiomas as observed by a physician provider and the subject. The investigators hypothesize that the two laser treatments will be an effective tool for treating cherry angiomas. The investigators aim to compare these modalities to electrodessication, as all three modalities are considered the current standard of care. Electrodessication can result in atrophic lesions at the site of the treated cherry angiomas. In summary, the goal of this project is to compare the non-ablative pulsed dye laser and the AuraTM potassium titanyl phosphate (KTP) laser to each other and to the current standard of care, electrodessication.
Conditions Studied
Interventions
- PROCEDURE Electrodessication
- PROCEDURE Pulsed dye laser (PDL)
- PROCEDURE potassium titanyl phosphate (KTP)
Study Locations (1)
Illinois
- Northwestern University - Chicago
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 15 participants |
| Start Date | 2006-09 |
| Est. Completion | 2007-10 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00791908
The ClinicalTrials.gov registry entry for NCT00791908 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 15 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Northwestern University, which has 1,209 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Cherry Angioma appearing as the primary indexed condition, and to 3 interventions - of which Electrodessication is the first listed.
NCT00791908 reports 1 study location spanning 1 distinct geographic area - top geographies include Illinois.
Frequently Asked Questions
What is clinical trial NCT00791908 about?
NCT00791908 is a clinical study titled "Comparison of Electrodessication, Potassium Titanyl Phosphate (KTP) Laser and Pulsed Dye Laser for Treatment of Cherry Angiomata". The primary objective of this study is to determine whether laser treatments over 6 weeks using the pulsed dye laser system or the potassium titanyl phosphate (KTP) laser are effective in patients with cherry angiomas as observed by a physician provider and the subject. The investigators hypothesiz...
What is the current status of trial NCT00791908?
This trial is currently completed. It is a NA study. The enrollment target is 15 participants. The study started on 2006-09. Estimated completion is 2007-10.
What conditions does trial NCT00791908 study?
This clinical trial studies the following conditions: Cherry Angioma.
What interventions are being tested in trial NCT00791908?
The interventions under investigation include: Electrodessication (PROCEDURE), Pulsed dye laser (PDL) (PROCEDURE), potassium titanyl phosphate (KTP) (PROCEDURE).
Who is sponsoring clinical trial NCT00791908?
This trial is sponsored by Northwestern University, which has 1,209 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00791908 being conducted?
This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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