[logo] HealthTree Foundation
search more_vert
close
person Sign In / Create Account
arrow_back

Go back to trials list

Renal Anhydramnios Fetal Therapy (RAFT) Trial


Description

Early pregnancy renal anhydramnios or EPRA is a condition where a pregnant woman does not have any amniotic fluid around her fetus because of a problem with the fetus's kidneys. This condition is thought to be fatal once the fetus is born because of inadequate lung growth. The Renal Anhydramnios Fetal Therapy (RAFT) Trial offers eligible pregnant women with a diagnosis of EPRA an experimental therapy of repeated or serial "amnioinfusions" of fluid into the womb. An amnioinfusion involves placing a small needle through the pregnant woman's skin into the womb next to the fetus. Warm sterile fluid with balanced electrolytes and antibiotics is then slowly infused into amniotic space inside the womb. The aim is to help the fetus's lungs grow enough so he or she can survive after birth. These amnioinfusions will be carried out by an expert in fetal interventions at a RAFT center. There is a significant risk of early rupture of membranes and early delivery in subjects who receive amnioinfusio

Trial Eligibility

Inclusion Criteria: 1. Confirmed anhydramnios before 22 weeks GA for patients with fetal renal failure (excluding bilateral renal agenesis) 2. Consent is signed and first therapeutic amnioinfusion can and does occur before 26 weeks and 0 days GA 3. Confirmation that the expectant mother does not wish to undergo termination of the pregnancy 4. Age ≥ 18 years of age for expectant mothers 5. Willingness to be followed and deliver at a RAFT center 6. Willingness for postnatal care to be performed at a RAFT center until discharge 7. Completed consults with Pediatric Nephrology, Neonatology, Transplant Surgery, Pediatric surgery, Maternal-Fetal Medicine Specialist, and Licensed Clinical Social Worker and a Genetic Counselor Exclusion Criteria: 1. Cervix less than 2.5 cm in length 2. No significant pathogenic or likely significant pathogenic findings on Karyotype or Microarray 3. Other significant congenital anomalies in the fetus 4. Evidence of chorioamnionitis or abruptio placentae 5. Evidence of rupture of membranes or chorioamniotic separation 6. Evidence of preterm labor 7. Multiple gestation 8. Severe maternal medical condition in pregnancy. 9. Maternal depression as assessed by a Beck Depression Inventory score equal to or greater than 17 that is refractory to treatment 10. Technical limitations precluding amnioinfusion

Study Info

Organization

Johns Hopkins University


Primary Outcome

Proportion of neonates surviving to >= 14 days and placement of dialysis access after serial amnioinfusions (defined as use of a dialysis catheter for >=14 continuous days)


Outcome Timeframe Birth to either survival to >=14 days and placement of dialysis access, or nonsurvival, up to 3 weeks

NCTID NCT03101891

Phases PHASE1

Primary Purpose TREATMENT

Start Date 2018-12-21

Completion Date 2025-04-01

Enrollment Target 70

Interventions

PROCEDURE Serial amnioinfusions with isotonic fluid

DEVICE Spinal needle

DRUG Isotonic fluid

Locations Recruiting

University of Southern California/Children's Hospital of Los Angeles/Huntington Hospital

United States, California, Los Angeles


University of California San Francisco

United States, California, San Francisco


Stanford University

United States, California, Stanford


University of Colorado Denver

United States, Colorado, Aurora


Johns Hopkins Hospital

United States, Maryland, Baltimore


Interested in joining this trial?

Our dedicated patient navigators are here to guide you through the validation and enrollment process with ease.

newsletter icon

Get the latest thought leadership on your Kidney Disease delivered straight to your inbox

Subscribe to the weekly newsletter for news, stories, clinical trial updates, and helpful resources and events with cancer experts.