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.

NCT06634719

Juveena Hydrogel System Feasibility Study for Heavy Menstrual Bleeding (HMB)

Completed
NAAges 18–45InterventionalDevice feasibility
Rejoni Inc.
~13 participants
Updated 2026-08-06 on ClinicalTrials.gov
What's tested:Juveena Hydrogel System

At a glance

Recruiting sites
0 of 3 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Primary Effectiveness Endpoint
Measured over Within 7 days post-treatment
Heavy Menstrual Bleeding

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.

This trial hasn't published a contact. View it on ClinicalTrials.gov

  • Primary Effectiveness EndpointWithin 7 days post-treatment

    Feasibility for invoking a tamponade effect