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NCT01285947 · ClinicalTrials.gov registry record · NA
Comparing the Pain Experience Between Patients Who Have and Who Have Not Undergone Dermatologic Procedures
A NA study, sponsored by Northwestern University.
- Completed
- Registry status
- NA
- Development phase
- 20
- Enrollment target
NCT01285947 is a NA study that has completed, run by Northwestern University. The registered enrollment target is 20 participants.
The verdict
NCT01285947, a NA study, has completed, sponsored by Northwestern University.
- COMPLETED
- Registry status
- NA
- Development phase
- 20 participants
- Enrollment target
Study Summary
The purpose of this study is to compare the pain experience of patients who have not had dermatologic procedures (previously "unexposed") using energy devices (lasers, radiofrequency, ultrasound, etc.) with patients who have previously had procedures (previously "exposed") using energy devices. Based on previous clinical encounters, individuals with no prior experience with cosmetic procedures appear to experience more pain. However, no study to date has thoroughly examined this observation. As a result, this study has been designed to find a possible difference in pain perception between previously exposed and unexposed patients undergoing cosmetic procedures using energy devices.
Interventions
- DEVICE Thermage
- OTHER Needle Application
- DEVICE VBeam Laser
- DEVICE Ulthera
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2011-02 |
| Est. Completion | 2011-05 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01285947
The ClinicalTrials.gov registry entry for NCT01285947 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 20 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 0 conditions, and to 4 interventions - of which Thermage is the first listed.
NCT01285947 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01285947 about?
NCT01285947 is a clinical study titled "Comparing the Pain Experience Between Patients Who Have and Who Have Not Undergone Dermatologic Procedures". The purpose of this study is to compare the pain experience of patients who have not had dermatologic procedures (previously "unexposed") using energy devices (lasers, radiofrequency, ultrasound, etc.) with patients who have previously had procedures (previously "exposed") using energy devices. Base...
What is the current status of trial NCT01285947?
This trial is currently completed. It is a NA study. The enrollment target is 20 participants. The study started on 2011-02. Estimated completion is 2011-05.
What interventions are being tested in trial NCT01285947?
The interventions under investigation include: Thermage (DEVICE), Needle Application (OTHER), VBeam Laser (DEVICE), Ulthera (DEVICE).
Who is sponsoring clinical trial NCT01285947?
This trial is sponsored by Northwestern University, which has 1,209 total clinical trials registered on ClinicalTrials.gov.
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