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Juveena Hydrogel System Feasibility Study for Heavy Menstrual Bleeding (HMB)
NCT06634719 · View on ClinicalTrials.gov ↗
Study Summary
This is a prospective, multicenter, single-arm interventional feasibility study to evaluate the safety and feasibility of the Juveena Hydrogel System for temporary control of heavy menstrual bleeding (HMB) in women with a history of chronic ovulatory HMB.
Conditions Studied
Interventions
- DEVICE Juveena Hydrogel System
Study Locations (4)
Arizona
- Arizona Gynecology Consultants — Phoenix
Arkansas
- Applied Research Center of Arkansas — Little Rock
New Jersey
- Rubino OB/GYN (Axia Women's Health) — West Orange
Ohio
- Seven Hills Clinical Research Group, LLC — Cincinnati
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 7 participants |
| Start Date | 2025-02-01 |
| Est. Completion | 2025-12-31 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06634719
The ClinicalTrials.gov registry entry for NCT06634719 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 7 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Rejoni, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Heavy Menstrual Bleeding appearing as the primary indexed condition, and to 1 intervention — of which Juveena Hydrogel System is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06634719 reports 4 study locations spanning 4 distinct geographic areas — top geographies include Arizona, Arkansas, New Jersey. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06634719 about?
NCT06634719 is a clinical study titled "Juveena Hydrogel System Feasibility Study for Heavy Menstrual Bleeding (HMB)". This is a prospective, multicenter, single-arm interventional feasibility study to evaluate the safety and feasibility of the Juveena Hydrogel System for temporary control of heavy menstrual bleeding (HMB) in women with a history of chronic ovulatory HMB.
What is the current status of trial NCT06634719?
This trial is currently recruiting. It is a NA study. The enrollment target is 7 participants. The study started on 2025-02-01. Estimated completion is 2025-12-31.
What conditions does trial NCT06634719 study?
This clinical trial studies the following conditions: Heavy Menstrual Bleeding. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06634719?
The interventions under investigation include: Juveena Hydrogel System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06634719?
This trial is sponsored by Rejoni, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06634719 being conducted?
This trial has 4 study locations across Arizona, Arkansas, New Jersey, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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