Optimizing Pharmacologic Treatment for Neonatal Opioid Withdrawal Syndrome (OPTimize NOW): A Symptom-Based Dosing Approach
Purpose
This clinical trial will help us learn more about how to best care for babies with Neonatal Opioid Withdrawal Syndrome, also called NOWS. Babies with NOWS often have tremors, a hard time sleeping, excessive crying, and trouble feeding. Some babies that have NOWS need medicine. Doctors have two ways of providing medicine that are widely used today: 1. Scheduled opioid taper approach. The baby gets medicine at regular times. As symptoms get better, the amount of medicine the baby gets decreases until the baby no longer needs medicine. This is called a medicine taper. 2. Symptom-based approach. The baby will only get medicine when they show signs of NOWS, instead of at regular times. If the baby is showing no signs of NOWS, no medicine will be given. We are doing the OPTimize NOW study to figure out the best way to give medicine to babies with NOWS.
Condition
- Neonatal Opiate Withdrawal Syndrome
Eligibility
- Eligible Ages
- Between 1 Hour and 48 Hours
- Eligible Genders
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- The infant is greater than or equal to 36 weeks gestation. 2. The infant had antenatal opioid exposure identified by at least one of the following: - History of maternal opioid use during pregnancy; - Positive maternal toxicology screen for opioids during the second or third trimester of pregnancy; and/or - Positive infant toxicology screen for opioids during the initial hospital stay. 3. The infant is being assessed and managed for NOWS at an eligible study site. 4. The infant is at risk for pharmacologic treatment for NOWS defined by either of the following - At least 1 score ≥ 8 if assessed and managed with FNAST or modification thereof - At least 1 "yes" if assessed and managed with the ESC care approach
Exclusion Criteria
- The infant has major birth defect(s). 2. The infant has neonatal encephalopathy (inclusive of hypoxic ischemic encephalopathy), a metabolic disorder, stroke, intracranial hemorrhage, or meningitis diagnosed prior to the initiation of pharmacologic treatment. 3. The infant is receiving respiratory support (any positive pressure or oxygen therapy) at 48 hours of age. 4. The infant has undergone major surgical intervention prior to or at 48 hours of age. 5. The infant has postnatal opioid exposure prior to the initiation of treatment for NOWS. 6. The infant was outborn and pharmacologic treatment was initiated at the transferring hospital. 7. The infant is assessed for eligibility during the study site's three-week washout period.
Study Design
- Phase
- Phase 3
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Crossover Assignment
- Intervention Model Description
- A two-period cluster crossover design will be used in this study. Study sites will be randomized in a 1:1 allocation ratio to one of two sequences: A three-week run-in period followed by a scheduled opioid taper approach for five months followed by a three-week washout period followed by a symptom-based dosing approach for five months. A three-week run-in period followed by a symptom-based dosing approach for five months followed by a three-week washout period followed by a scheduled opioid taper approach for five months.
- Primary Purpose
- Treatment
- Masking
- None (Open Label)
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Other Sequence 1 |
This sequence will assign eligible participants to a three-week run-in period followed by a scheduled opioid taper approach for five months followed by a three-week washout period followed by symptom-based dosing approach for five months. |
|
|
Other Sequence 2 |
This sequence will assign eligible participants to a three-week run-in period followed by a symptom-based dosing approach for five months followed by a three-week washout period followed by scheduled opioid taper approach for five months. |
|
Recruiting Locations
Birmingham, Alabama 35294
Namasivayam Ambalavanan, MD
Little Rock, Arkansas 72205
Richard Hall, MD
Wilmington, Delaware 19801
Tampa, Florida 33606
Indianapolis, Indiana 46202
Gregory Sokol, MD
Jeffersonville, Indiana 47130
Kansas City, Kansas 66160
Edgewood, Kentucky 41017
Stephanie Merhar, MD, MS
Lexington, Kentucky 40536
Louisville, Kentucky 40202
Louisville, Kentucky 40207
Omaha, Nebraska 68198
Ann Anderson Berry, MD, PhD
Atlantic City, New Jersey 08401
Albuquerque, New Mexico 87131
Lawrence Leeman, MD, MPH
Rochester, New York 14642
Cincinnati, Ohio 45202
Stephanie Merhar, MD, MS
513-803-5180
Cincinnati, Ohio 45229
Stephanie Merhar, MD, MS
513-803-5180
Oklahoma City, Oklahoma 73104
Philadelphia, Pennsylvania 19104
Philadelphia, Pennsylvania 19107
Philadelphia, Pennsylvania 19107
Walter Kraft, MD
Salt Lake City, Utah 84158
More Details
- NCT ID
- NCT05980260
- Status
- Recruiting
- Sponsor
- HELP for NOWS Consortium
Detailed Description
This two-period cluster crossover clinical trial will compare the length of time from birth until medically ready for discharge between infants with neonatal opioid withdrawal syndrome (NOWS) who are ≥ 36 weeks' gestation, at risk for pharmacologic treatment, and treated for NOWS with either a symptom-based dosing approach or a scheduled opioid taper approach. Each study site (i.e., cluster) will be randomized in a 1:1 allocation ratio to one of two sequences: - A three-week run-in period followed by a scheduled opioid taper approach for five months (Period 1) followed by a three-week washout period followed by a symptom-based dosing approach for five months (Period 2) - A three-week run-in period followed by a symptom-based dosing approach for five months (Period 1) followed by a three-week washout period followed by scheduled opioid taper approach for five months (Period 2) The randomization scheme will be stratified by the assessment and management approach used at each study site (i.e., Finnegan or Eat, Seep and Console).