Recruiting

Warm LR Amnioinfusion

Sponsor:

Medical College of Wisconsin

Code:

NCT07274527

Conditions

Neonatal Respiratory Distress Related Conditions

Meconium

Perinatal Morbidity

Neonatal Acidosis

Cord Blood

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Intrauterine pressure catheter

Standard obstetric care at discretion of delivery provider

Study Details

Brief summary:

Thick meconium in the amniotic fluid occurs in about one out of seven pregnancies and increases the chance that a newborn may have breathing problems after birth. These problems can include the need for oxygen, breathing support, admission to the neonatal intensive care unit (NICU), or, in severe cases, meconium aspiration syndrome or persistent pulmonary hypertension.

Although amnioinfusion or placing sterile fluid into the uterus during labor was previously studied as a way to reduce these complications, earlier research had major limitations. Past studies included all types of meconium, used different fluid types and temperatures, had inconsistent protocols, and did not measure biomarkers of inflammation or look at long-term outcomes. As a result, it is still unclear whether a modern, standardized approach to amnioinfusion can meaningfully improve newborn health when the meconium is truly thick.

The PEARL Trial is a randomized clinical trial designed to answer this question. The study will enroll pregnant individuals at or beyond 36 weeks of gestation who develop thick meconium-stained amniotic fluid, confirmed using a simple, objective measurement ("meconium-crit"). Participants will be randomly assigned to receive either:

Warm lactated Ringer's (LR) amnioinfusion through an intrauterine pressure catheter (IUPC), following a standardized protocol, or standard care without amnioinfusion.

The main goal is to determine whether warm LR amnioinfusion reduces short-term breathing problems in newborns. The study also collects umbilical cord blood at birth to evaluate markers of inflammation and potential brain injury, which may help explain why some infants develop complications. Families will also be contacted when their child is 12 months old to complete a developmental questionnaire that is widely used in pediatric practice.

By using a clear definition of thick meconium, a warm LR infusion protocol, fidelity checklists, and long-term follow-up, this trial aims to provide high-quality evidence to guide care in labor and delivery units nationwide.

Conditions

Neonatal Respiratory Distress Related Conditions

Meconium

Perinatal Morbidity

Neonatal Acidosis

Cord Blood

Study ID

NCT07274527

Start date

May 15, 2026

Status verified date

May, 2026

Completion date

Apr 15, 2030

Anticipated

Primary completion date

Apr 15, 2029

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Maternal age greater than or equal to 18 years old
  • Singleton pregnancy
  • Gestational age of greater than or equal to 36 weeks 0 days gestation
  • Cephalic presentation
  • Cercial dilation between 2-10 centimeters
  • Meconium

Exclusion Criteria:

  • Major fetal anomaly
  • Multiple gestation
  • Eunice Kennedy Shrive National Institute of Child Health and Human Developmet (NICHD) Category III fetal heart tracing
  • Contraindication to internal monitors
  • Prelabor premature ruptuore of membranes before 36 weeks 0 days gestation, - Inability to consent

Study Design

Enrollment

320 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Warm Lactated Ringer Amnioinfusion

Standardized warm amnioinfusion consisting of a 500 mL bolus of warmed (37°C) lactated ringer's infused over 30 minutes through an intrauterine pressure catheter (IUPC), followed by a continuous maintenance infusion of 125 mL/hour until the amniotic fluid clears or delivery. Re-administration is permitted if thick meconium persists or the deepest amniotic fluid pocket is <2 cm by ultrasound.

placebo comparator: Standard of Care

Standard obstetric care will be at the discretion of the delivery provider.

Interventions

Intrauterine pressure catheter

Standardized warm amnioinfusion consisting of a 500 mL bolus of warmed (37°C) lactated ringer's infused over 30 minutes through an intrauterine pressure catheter (IUPC), followed by a continuous maintenance infusion of 125 mL/hour until the amniotic fluid clears or delivery.

Standard obstetric care at discretion of delivery provider

Route obstetric care at discretion of delivery provider

Primary outcome measure

  • Number of participants with composite neonatal respiratory morbidity [ Time Frame: 72 hours after delivery ]

Central Contacts and Locations

Locations

Froedtert Hospital and Medical College of Wisconsin Birth Center

Recruiting

Milwaukee, Wisconsin, United States, 53045

Contacts

Polnaszek Assistant Professor and Principal Investigator, MD MPH

414-805-6600bpolnaszek@mcw.edu

More Information

Sponsor

Medical College of Wisconsin

Last update posted

May 19, 2026

Last verified

May, 2026

Keywords

  • Amnioinfusion
  • Meconium
  • Neonatal morbidity
  • Developmental Screening
  • Maternal Morbidity
  • Neonatal respiratory morbidity
  • Umbilical cord gas and biomarkers
  • Healthcare Utilization

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-08. This information was provided to ClinicalTrials.gov by Medical College of Wisconsin on 2026-05-19.