Trials / Active Not Recruiting
Active Not RecruitingNCT07086248
A Study to Determine if RADIESSE® Dilute Treatment in Décolleté of Adult Women Affects Radiographic Imaging Assessments
An Open-label, Multicenter, Single-arm, Uncontrolled Safety Study to Assess Radiographic Imaging Following Treatment With RADIESSE® Dilute in the Décolleté in Adult Females in the United States
- Status
- Active Not Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 30 (actual)
- Sponsor
- Merz North America, Inc. · Industry
- Sex
- Female
- Age
- 40 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
The primary purpose of this study is to determine if treatment with Radiesse dilute in the décolleté interferes with radiographic imaging of the breast tissue.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Radiesse | Radiesse injections diluted 1:2 with sterile saline. |
Timeline
- Start date
- 2025-07-22
- Primary completion
- 2026-01-26
- Completion
- 2026-10-01
- First posted
- 2025-07-25
- Last updated
- 2026-03-09
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT07086248. Inclusion in this directory is not an endorsement.