Evaluation of Satisfaction in Patients Undergoing Non Surgical Lifting by Means of Coned Wires.

Completed

• Conditions: Complications; Pain

• Registration Number: NCT02347826
• Lead Sponsor: AQ-DE

Brief Summary

An email questionnaire about subjective satisfaction and discomfort has been sent to 243 patients undergoing non-surgical facial and cervical lift 1 week, 1 month, 6 months and 1 year after treatment.

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 Timeline

• Study Start: 2014-01
• Primary Completion: 2014-01
• Study Completion: 2014-12
• Status Verified: 2015-01
• Study First Submitted: 2015-01-21
• Study First Submitted QC: 2015-01-26
• Study First Posted: 2015-01-27
• Last Update Submitted: 2015-01-27
• Last Update Posted: 2015-01-28

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 243

Inclusion Criteria

• Patients undergoing facial and cervical non surgical lift by means of resorbable coned wires

Exclusion Criteria

• Patients with asymmetry

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Subjective satisfaction questionnaire	up to one year

Secondary Outcome Measures

Name	Time	Method
Discomfort related to treatment questionnaire	one week, one month, 6 months, one year

Trial Locations

Locations (1)

AQCE; 🇮🇹 Milan, Lombardia\Milan, Italy