CClinicalTrials.gg
TerminatedNCT02023307Updated Sep 2, 2015

Use of V-Loc Suture for Mid-face Lifting in Short-flap Rhytidectomy

An interventional study of V-Loc Suture in Use of the Vloc Suture and Elevation of the Mid-face, sponsored by Lifestyle Lift. Terminated at 1 site in United States. Open to participants aged 18 Years to 95 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2015-09-02.

Sponsored by Lifestyle Lift · Not applicable, Interventional, and Treatment

Why this study was terminated
Clinic Closed
Phase
Not applicable
Study type
Interventional
Enrollment
15
Allocation
Not applicable
Ages
18 Years to 95 Years
Sex
All
01

Study summary

This study will evaluate and measure the Vloc suture's ability to elevate the mid-face when using a short flap, short incision technique in during a traditional face-lift. The objective of this study is to assess the suture's potential in elevating the mid-face when a traditional Lifestyle facelift is performed. We hypothesize that the Vloc suture will elevate the mid-face more effectively when using a short flap, short incision technique on a traditional facelift.

Read the detailed description

A total of 25 patients who are already receiving a traditional Lifestyle Lift will be asked to participate. Once the consent form has been signed by the patient, the facelift will be performed as scheduled and the Vloc suture will be added to the mid-face area. Each patient will be added to a database and their progress will be tracked with photos taken before, at 6 weeks, and at 6 months following the procedure. All data stored will be locked into a hard drive that can only be accessed by the research staff and the doctor. The text data will be used by research staff for reports and articles.

* you must already have purchased and scheduled a facelift procedure with Lifestyle Lift to participate in this trial. The addition of only the V-loc suture is at no cost.

02

Conditions studied

  • Use of the Vloc Suture
  • Elevation of the Mid-face
03

In context

Lead sponsor

This is the only study on the registry with Lifestyle Lift as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 95 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Patients who are scheduled to receive a Lifestyle Lift will be asked to participate. The first 25 patients who have consented will be included into the study.

Exclusion criteria

Exclusion Criteria:

  • Any patient who is not able to receive a facelift for whatever reason, or who do not want a facelift will not be apart of this study
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
15 participants (actual)

Study arms

  • Experimental
    Rhytidectomy with Covidien

    25 patients receiving a mid-face lift in short-flap rhytidectomy

    Device: V-Loc Suture

Interventions

  • DeviceV-Loc Suture

    Also known as: Covidien

06

What researchers measure

Primary outcomes

  1. Elevation of the mid-face

    Time frame: Initial- 6 weeks

Secondary outcomes

  1. No Retention of Mid-face

    Time frame: initial-6 Months

07

Study locations

1 site
  • Lifestyle Lift
    Albuquerque, New Mexico 87110, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 2, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02023307
Lead sponsor
Lifestyle Lift
Responsible party
Sponsor
First posted
Dec 30, 2013
Start date
Feb 2014
Primary completion
Aug 2015
Completion
Aug 2015
Last update
Sep 2, 2015

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Aug 2015. You cannot join it, but the record below documents what was studied.

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