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OpenTrials
Completed

NCT Number: NCT02347826

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

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.

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Key information

Age range

19 year–76 year

Sex eligibility

All sexes

Study type

Observational

Primary location

AQCE

Milan, Lombardia\Milan, 20123, Italy

About this study

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

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • Patients with asymmetry

Treatment and study plan

Primary outcomes

  1. Subjective satisfaction questionnaire

    Time frame: up to one year

Secondary outcomes

  1. Discomfort related to treatment questionnaire

    Time frame: one week, one month, 6 months, one year

Sponsors and collaborators

Lead sponsor

AQ-DE

Other

Registry information

Official study title

Evaluation of Aesthetic Satisfaction in Patients Undergoing Non Surgical Face and Neck Lift by Means of Coned Wires.

Acronym: SCW

Important dates

Study start
2014
Primary completion
2014
Study completion
2014
First posted
Jan 27, 2015
Registry last updated
Jan 28, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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