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Completed No phase listed Observational

RUBY Post-Market Registry on the Jada® System

ClinicalTrials.gov ID: NCT04995887

Public ClinicalTrials.gov record NCT04995887. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 5:03 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

RUBY: Treating Abnormal Postpartum Uterine Bleeding or Postpartum Hemorrhage With the Jada® System - A Post-Market Registry

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The RUBY Study is a multicenter, observational, post-market registry designed to collect observational data on patients treated with the Jada System in the post-market setting.

Study identification

NCT ID
NCT04995887
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Alydia Health
Industry
Enrollment
809 participants

Conditions and interventions

Interventions

Device

Eligibility (public fields only)

Age range
Not listed
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 1, 2020 (Actual)
Primary completion
Mar 31, 2022 (Actual)
Completion
Apr 30, 2022 (Actual)
Last update posted
Aug 22, 2022

2020 – 2022

United States locations

U.S. sites
16
U.S. states
11
U.S. cities
14
Facility City State ZIP Site status
Loma Linda University Loma Linda California 92354 —
ChristianaCare Newark Delaware 19718 —
Northeast Georgia Medical Center Gainesville Georgia 30501 —
Oshsner Baptist New Orleans Louisiana 70115 —
Allina (Abbott Northwestern) Minneapolis Minnesota 55409 —
Long Island Jewish Medical Center New Hyde Park New York 11040 —
Mount Sinai New York New York 10029 —
Nyph/Cumc New York New York 10032 —
University Hospitals Cleveland Ohio 44106 —
Cleveland Clinic Cleveland Ohio 44195 —
The Ohio State University Columbus Ohio 43210 —
Ohio Health Gahanna Ohio 43230 —
UPMC - Magee Women's Hospital Pittsburgh Pennsylvania 15213 —
Charleston Birth Place Mt. Pleasant South Carolina 29464 —
University of Utah Salt Lake City Utah 84132 —
Charleston Area Medical Center Charleston West Virginia 25302 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04995887, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 22, 2022 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04995887 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →