- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02347826
Evaluation of Satisfaction in Patients Undergoing Non Surgical Lifting by Means of Coned Wires. (SCW)
Evaluation of Aesthetic Satisfaction in Patients Undergoing Non Surgical Face and Neck Lift by Means of Coned Wires.
Study Overview
Status
Conditions
Detailed Description
243 patients underwent non-surgical coned wires (silhouette soft) facial and cervical lift between October 2013 and November 2014. The procedures has been executed in our aesthetic clinics in Milan, Bologna, Turin, Genoa, Rome, Asti, San Remo and Palermo.
Among the 243 patients, 217 were females and 26 males, with age ranging from 19 to 76 years. 103 patients underwent only facial lift, of which 12 only in the frontal area, 61 only on cheek and malar area, and 30 on both the areas.
39 patients underwent only cervical lift, of those 14 by means of appliance of 1 or 2 wires, 25 by means of appliance of more than 2 wires.
101 patients underwent both facial and cervical non surgical lift. We sent to every patient a email questionnaire1 week, 1 month, 6 months and 1 year after treatment.
In the questionnaire, patients has been asked to enter a value between 1 and 5 about subjective satisfaction regarding the aesthetic improvement (ranging from 1, poor, to 5, excellent), and discomfort related to treatment (ranging from 1, no perceived discomfort, to 5, impossibility to execute working and social activities).
The data has been analyzed and related to other factors such as:
- number of wires applied on each patient
- other aesthetic or regenerative medicine treatments executed on the same patient on the same year
- total expenditure related to aesthetic treatments in the same year
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Lombardia\Milan
-
Milan, Lombardia\Milan, Italy, 20123
- AQCE
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients undergoing facial and cervical non surgical lift by means of resorbable coned wires
Exclusion Criteria:
- Patients with asymmetry
Study Plan
How is the study designed?
Design Details
- Time Perspectives: Retrospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Subjective satisfaction questionnaire
Time Frame: up to one year
|
up to one year
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Discomfort related to treatment questionnaire
Time Frame: one week, one month, 6 months, one year
|
one week, one month, 6 months, one year
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Mario Goisis, MS, AQ-DE
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Aqde
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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