Juveena Hydrogel System for Heavy Menstrual Bleeding
This study is looking at a new treatment called the Juveena Hydrogel System for women who experience heavy menstrual bleeding (HMB). HMB is when your period is unusually heavy and affects your daily life. The Juveena Hydrogel System is a single-use device that is placed inside the uterus as a liquid and quickly turns into a gel. Researchers want to see if it's safe and works well to temporarily control HMB. You might be able to join if you are a woman between 18 and 45 years old and have a recent history of HMB that impacts your quality of life. The main goal is to see how well the system works within 7 days after treatment. The study is currently recruiting a small number of participants.
- Study design
- This is a single-arm study, meaning all participants will receive the Juveena Hydrogel System. It plans to enroll 7 women.
- What's involved
- You will have a baseline evaluation, receive the Juveena HS treatment, and keep a diary. There will be phone calls on Days 1, 14, and 56 after treatment, and clinic visits on Day 7 and Day 28.
- Compensation
- Not stated in the trial record.
- Follow-up
- You will be followed for at least 56 days after treatment, with the primary effectiveness measured within 7 days.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Juveena Hydrogel System Feasibility Study for Heavy Menstrual Bleeding (HMB)
At a glance
Conditions
NCT06634719
Where you'd take part
This study runs at 3 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Applied Research Center of Arkansas
Little Rock, Arkansasno site contact published
Rubino OB/GYN (Axia Women's Health)
West Orange, New Jerseyno site contact published
Seven Hills Clinical Research Group, LLC
Cincinnati, Ohiono site contact published
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
What this trial measures
- Primary Effectiveness EndpointWithin 7 days post-treatment
Feasibility for invoking a tamponade effect