NCT05746078Active, not recruiting
Performance and Safety Assessment of SPRING THREAD® Elastic Tensor Thread in Patients With Mild to Moderate Facial Ptosis.
Long-term Assessment of the Performance and Safety of SPRING THREAD® Elastic Tensor Thread.
Source: ClinicalTrials.gov · Last updated 30 Sept 2026
Brief summary (registry, in English)
The purpose of this post-market clinical follow up study is to assess the safety and effectiveness of the SPRING THREAD® elastic tensor thread. The study will evaluate the outcome of the SPRING THREAD® elastic tensor thread range over a period of 5 years.
- Status (registry)
- Active, not recruiting
- Study type
- Observational
- Enrollment
- 99 (estimated)
- First submitted
- 17 Feb 2023
- Start date
- 16 Feb 2023
- Primary completion date
- 7 Feb 2026
- Lead sponsor
- 1st SurgiConcept
- NCT number
- NCT05746078
What you commit to
- Study type: Observational
- Planned participants: 99
- From 16 Feb 2023 to the primary completion date, 7 Feb 2026
- 2 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Patients who have had a previous facial rejuvenation treatment in the 3 months prior to the study.
- Patients treated with long-term systemic corticosteroids.
- Patient participating or having participated in another clinical trial protocol, drug or medical device within 30 days of inclusion.
Other illness
- Patients with visceral failure, chronic immunological pathology, pregnant or breasfeading women.
Other
- Patient unable to understand study information and attend study visits.
- Patient did not give consent to participate.
- Patient refusing to participate in the clinical investigation.
Who the study is looking for
- Men / women aged 35 to 75 with facial ptosis (cheekbones, jowls) with or without a history of aesthetic treatment (botox, filler, surgical lift).
- Patient able to understand the explanations given.
- Patient informed and not objecting to participate in the study.
- Patient able to comply with protocol requirements, including follow-up visits.
- Patient affiliated to social security.
Age in the registry: 35 years to 75 years · Sex: All · Does not accept healthy volunteers
Sites (2)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Hopital Henri Mondor Coordinator of this site? Confirm its status | Créteil | France | Unknown status |
| Hopital Pierre Paul Riquet Coordinator of this site? Confirm its status | Toulouse | France | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.