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Corticosteroid

Dexamethasone + IVIG for Fetal AV Block

Phase 3
Recruiting
Led By Bettina Cuneo, MD
Research Sponsored by NYU Langone Health
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Located within 6 hours drive of the participating pediatric cardiology site
Be <18 weeks pregnant at the time of enrollment
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 year post-birth
Awards & highlights

Study Summary

This trial is investigating a way to improve the treatment of a heart condition called fetal complete atrioventricular block (3° AVB). This heart condition is almost always caused by a mother's antibodies, and it is fatal in 1/5 of cases. Current treatment for 3° AVB is not effective, so this trial is testing a new way to treat it.

Who is the study for?
This trial is for pregnant women over 18 with high levels of anti-Ro antibodies, which are linked to fetal heart block. They must be able to monitor the baby's heart rate at home, send audio texts, live within a 6-hour drive of the cardiology site, and take oral medication. It excludes those with multi-fetal pregnancies or known allergies to the study drugs.Check my eligibility
What is being tested?
The STOP BLOQ trial tests if early detection and treatment can prevent severe fetal atrioventricular block in babies whose mothers have specific autoantibodies. It involves risk assessment, home monitoring by mothers, and rapid treatment with Dexamethasone or IVIG upon detecting abnormalities.See study design
What are the potential side effects?
Dexamethasone may cause increased blood sugar levels, mood changes, stomach ulcers or increased appetite. IVIG might lead to mild flu-like symptoms such as fever or muscle aches; more rarely it could cause allergic reactions or impact kidney function.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I live within a 6-hour drive of the pediatric cardiology site.
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I am less than 18 weeks pregnant.
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I am 18 years old or older.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 year post-birth
This trial's timeline: 3 weeks for screening, Varies for treatment, and 1 year post-birth for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Percentage of 2° AVB subjects with NR (1:1 AV conduction) at birth
Secondary outcome measures
Incidences of isolated extra-nodal cardiac disease
Percentage of 2° AVB subjects who maintain NR at age 1 year.
Percentage of AV interval > 170 msec subjects with NR at birth

Side effects data

From 2020 Phase 3 trial • 105 Patients • NCT03065244
45%
Continued Fever after treatment completion and crossover to other study treatment
20%
Hemolytic Anemia
10%
Rash
8%
GI Symptoms
8%
Arthritis/pain and swelling in extremities
6%
Fever after discharge not attributed to KD
6%
Epistaxis
6%
Fever following crossover treatment
4%
Headache
4%
URI
100%
80%
60%
40%
20%
0%
Study treatment Arm
IVIG
Infliximab

Trial Design

1Treatment groups
Experimental Treatment
Group I: Mothers with Fetuses Who Have 2° AVB or AV interval > 170msExperimental Treatment2 Interventions
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Dexamethasone
2007
Completed Phase 4
~2590
IVIG
2016
Completed Phase 4
~2970

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for Atrioventricular Block (AVB) include sympathomimetic drugs and corticosteroids. Sympathomimetic drugs, such as isoproterenol, work by stimulating beta-adrenergic receptors to increase heart rate, which is essential in managing bradycardia associated with AVB. Corticosteroids like dexamethasone may not directly affect the heart rate or AV block but can improve the clinical tolerance of conduction disturbances. These treatments are vital for AVB patients as they help maintain an adequate heart rate and prevent the progression of the block, thereby reducing the risk of severe complications and improving patient outcomes.
[Use of sympathomimetic agents in fetal atrioventricular heart block].[Use of high doses of atropine during dipyridamole echocardiography: safety and efficacy of the combined test].Ivabradine for chronic heart rate control in persistent atrial fibrillation. Design of the BRAKE-AF project.

Find a Location

Who is running the clinical trial?

NYU Langone HealthLead Sponsor
1,375 Previous Clinical Trials
839,491 Total Patients Enrolled
Bettina Cuneo, MDPrincipal InvestigatorUniversity of Colorado, Denver
Jill Buyon, MDPrincipal InvestigatorNYU Langone Health
1 Previous Clinical Trials
307 Total Patients Enrolled

Media Library

Dexamethasone (Corticosteroid) Clinical Trial Eligibility Overview. Trial Name: NCT04474223 — Phase 3
Atrioventricular Block Research Study Groups: Mothers with Fetuses Who Have 2° AVB or AV interval > 170ms
Atrioventricular Block Clinical Trial 2023: Dexamethasone Highlights & Side Effects. Trial Name: NCT04474223 — Phase 3
Dexamethasone (Corticosteroid) 2023 Treatment Timeline for Medical Study. Trial Name: NCT04474223 — Phase 3
~451 spots leftby Aug 2026