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Neonatal Abstinence SyndromePhase 4NCT03092011

Treatment of Neonatal Abstinence Syndrome With Clonidine Versus Morphine as Primary Therapy

A Phase 4 study testing Clonidine and Morphine Sulfate in people with Neonatal Abstinence Syndrome, run by Cooper Norcross Health at 1 site in United States.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

The purpose of this study is to show non-inferiority between two medications used for medical treatment of withdrawal seen in Neonatal Abstinence Syndrome (NAS), Clonidine and Morphine Sulfate (used in routine care) on length of treatment for NAS . Read more about this study

Who is it for?
Ages Up to 10 days
Conditions the study is for
Neonatal Abstinence Syndrome
What is being tested?
Clonidine and Morphine Sulfate
Could I receive a placebo?
No, everyone receives an active treatment
How many people
69 participants
Where
1 siteUnited States
Study dates
21 Feb 2018to 1 Dec 2026
Phase
Phase 4
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Up to 10 days
  • All sexes
  • No healthy volunteers
  • Child

Who may be able to join

  • Born at Cooper University Hospital
  • Greater than or equal to 35 weeks gestation age
  • Admitted to the NICU or Transitional nursery
  • Mothers admitted to using illicit substances or prescription medications (which can result in withdrawal symptoms) while pregnant and/or had a positive urine drug screen during pregnancy.
  • Babies being started on medication to control withdrawal symptoms of NAS.
  • No congenital anomalies or neurologic condition (i.e. hypoxic-ischemic encephalopathy, seizures, meningitis etc.)

Who cannot join

  • Premature infants <35 week gestational age
  • Infants with major congenital abnormalities
  • Blood pressure instability
  • Major medical conditions

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Cooper University Hospital

    Camden, New Jersey, 08103

Other trials in United States

About this study

The purpose of this study is to show non-inferiority between two medications used for medical treatment of withdrawal seen in Neonatal Abstinence Syndrome (NAS), Clonidine and Morphine Sulfate (used in routine care) on length of treatment for NAS .

Read the detailed description

Prospective randomized control trial. There will be 2 groups, control group and the intervention group. The control group will receive the standard of care used for NAS treatment currently in Cooper Hospital NICU and transitional nursery.

Morphine is used as the standard treatment and if the withdrawal symptoms are not well controlled, Phenobarbital may be added as a rescue therapy at that time. Hence, both the Morphine and Phenobarbital are part of the standard treatment at Cooper University Hospital for NAS. The intervention group will be treated with Clonidine for withdrawal symptoms of NAS and if not well controlled with Clonidine then Phenobarbital will be added as a rescue therapy.

All of the medications, Clonidine, Morphine and Phenobarbital will be administered orally via syringe, prior to initiation of a feed.

The following are the treatment guidelines (see attached for more details):

  1. Observe babies exposed to narcotics in utero in the hospital for a minimum of 72 hours to 5 days prior to discharge, to monitor for possible withdrawal symptoms.
  2. Once infants are exhibiting signs of withdrawal, the infants will be scored using Modified Finnegan Scoring System every four hours after feeds:
  3. If a score is 8 or higher, scoring will be done every 2 hours
  4. If three consecutive scores are less than 8, scoring will go back to every four hours, after feeds
  5. The subjects will be scored from a minimum of 6 hours.
  6. Treatment will be initiated if there are three consecutive scores of 8 or higher.
  7. For each baby undergoing NAS scoring, and if therapy needs to be initiated, then physical and occupational therapy will be consulted.
  8. Blood pressure and heart rate will be checked by the bedside nurse and documented once treatment is started (timing of every 3 or every 4 hours will depend on feeding schedule of the baby) and continued as follows:
  9. Check every three or four hours (with hands on care) for the first 24 hours (day 1 of medication) of treatment.
  10. Check every eight hours (or 6 hours with care) for the next 24 hours (day 2 of medication).
  11. Check every twelve hours for day 3 of treatment and until discontinuation of therapy.
  12. Check every twelve hours for 24 hours after the discontinuation of the medication.
  13. If the infant is started on medication at less than 7 days of age, the birth weight will be used for medication dosing throughout the study, for weaning and for increasing the dose. If the infant is started on medication after 7 days of life, then the current weight will be used for initiation of medication dose and the same weight will be used throughout the study, and for increases and weaning of the medication dose.
  14. Mother/guardian of the baby will be approached as soon as it is determined that the baby may be at risk for NAS once he/she is born and the consent obtained at that time. This may be before or after baby's birth but before initiation of medical/pharmacological treatment of NAS.
  15. Randomization to the standard therapy group (Morphine group) versus intervention group (Clonidine group).
  16. When the patient is determined to need pharmacological treatment for NAS by the treating physician, a member of the research team will be notified.
  17. Presence of consent will be verified, or consent obtained.
  18. Randomization procedure will take place.
  19. The nurses, parents, and the medical staff directly taking care of the patient will be blinded and be unaware of specific group the patient is randomized to.
  20. Start Medication
  21. Standard Group: Start oral (PO/NG/OG) Morphine Sulfate at 0.03 mg/kg/dose every 3 hours or 0.04 mg/kg/dose every 4 hours depending on baby's feeding schedule.
  22. Intervention Group: Start oral (PO/NG/OG) Clonidine HCl (Catapress) at 0.38 mcg/kg/dose every 3 hours or 0.5 mcg/kg/dose every 4 hours depending on baby's feeding schedule.
  23. Continue scoring as per standard protocol using the Modified Finnegan Scoring Tool.
  24. Do not wean the medication for the first 24 hours, even if the scores are low
  25. For three consecutive scores of 8 or greater, or 2 scores of greater than or equal to 13:
  26. Increase the dose of the medication by 25% of the previous dose.
  27. If there is one Finnegan score of 12 or greater or consecutive scores over 8, may give one rescue dose 1-2 per 24 hours (of whichever medication the patient is receiving):
  28. Morphine 0.02 mg/kg
  29. Clonidine 0.25 mcg/kg
  30. If there are 3 consecutive scores higher than 8 and if:
  31. Clonidine needs to be increased greater than 4 times, may add Phenobarbital Sodium (65 mg vial or 130 mg vial depending the dose which is based on the weight of the patient) oral (PO/NG/OG) at 5 mg/kg/day divided BID = 2.5 mg/kg, every 12 hours. No loading doses.
  32. Morphine needs to be increased greater than 4 times, may add Phenobarbital oral (PO/NG/OG) at 5 mg/kg/day divided BID = 2.5 mg/kg, every 12 hours. No loading doses.
  33. Do not weight adjust Phenobarbital unless the patient's NAS symptoms are not stable or there is difficulty weaning Clonidine or Morphine.
  34. Clonidine or the Morphine will not be weight adjusted as the patient continues to grow and gain weight.
  35. Once patient is stable (scores <8 for 24-48 hours), Clonidine/Morphine will be decreased by 10% of the highest dose using the original/birth weight (same amount each time) every 24 to 48 hours, provided the scores remain below 8.
  36. Example: If started at 0.04 mg/kg based on 2 kg, will wean by 0.004 mg/kg, using 2 kg.
  37. Discontinue medication (notified by the pharmacist when reach the discontinuation dose) when:
  38. Clonidine - dose is at 0.15 mcg/kg/dose Q3h or 0.2 mcg/kg/dose Q4h (1 mcg/kg/day). The dosing interval depends on the feeding schedule of the patient.
  39. Morphine - dose is at 0.015 mg/kg/dose Q3h or 0.02 mg/kg/dose Q4h (1 mg/kg/day). The dosing interval depends on the feeding schedule of the patient.
  40. Monitor for a minimum of 24 hours by checking and documenting standard NICU vitals (heart rate, blood pressure, respirations, temperature), and Modified Finnegan Scores after the medication is discontinued prior to discharging home. All patients in the NICU are monitored continuously using cardiopulmonary monitors which include monitoring for heart rate, blood pressure, respiratory rate and oxygen saturation. Treating physician will be evaluating these vital signs.
  41. Signs of rebound hypertension may be seen within 24 hours after discontinuation of Clonidine.10,11,13 Treating physician will be evaluating for this, as well as standard vitals in all patients for 24 hours after discontinuation of therapy.
  42. As per Lexicomp:35 i. The half-life in children is 6.13 + 1.33 hours. ii. Discontinuation of therapy: Gradual withdrawal is needed (taper oral immediate release or epidural dose gradually over 2 to 4 days to avoid rebound hypertension). The Clonidine withdrawal syndrome is more pronounced after abrupt cessation of long term therapy than after short-term therapy (1 to 2 months). It has usually been associated with previous administration of high oral doses (>1.2 mg daily in adults) and /or continuation of beta-blocker therapy. Blood pressure may increase 8 to 24 hours after last dose.
  43. In our study we will be weaning Clonidine over a period of time and by the time Clonidine is discontinued it will be less than ½ of the smallest therapeutic dose. Blood pressure will be monitored for the whole duration of Clonidine wean.
  44. Blood pressure instability (hypotension and hypertension) will be defined as per the figures attached at the end of the protocol.
  45. The blood pressure ranges are as following:36
  • Systolic Blood Pressure (SBP) (Using the range from 35 weeks to 44 weeks)
  • Minimum: 50-70 mmHg
  • Maximum: 85-110 mmHg
  • Diastolic Blood Pressure (Using the range from 35 weeks to 44 weeks)
  • Minimum: 25-45 mmHg
  • Maximum: 55-70 mmHg
  1. If the systolic blood pressure is more than 113 mmHg on 3 consecutive readings, then this will be considered hypertension.36
  • The blood pressure will be measured in the right upper arm. Three consecutive readings at 2 minute interval will be measured.37,38 If the average of the three readings of the SBP is more than 113 mmHg, then this will meet the requirement for the definition of hypertension. Medical treatment will be initiated for hypertension.
  • Hydralazine is one of the most commonly used medication used for hypertension in neonates.38
  • Hydralazine (PO/NG/OG) 0.25 to 1 mg/kg/dose every 6 to 8 hours; maximum dose 7.5 mg/kg/day37,39
  • Blood pressure and heart rate will continue to be monitored.
  1. Infants may be discharged on Phenobarbital.
  2. All children in the study will be followed for developmental outcomes until 2 years of age.
  3. Bayley screen results at 18-24 months will be collected when available, and patients will be contacted at 6 months, 12 months and 24 months for ASQ.
Being tested
Clonidine, Morphine Sulfate
Medical subject headings
Neonatal Abstinence Syndrome

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • ClonidineDrug

    Clonidine at 0.38 mcg/kg/dose every 3 hours or 0.5 mcg/kg/dose every 4 hours Clonidine dose will be increased by 25% of the previous dose if needed. It will be decreased by 10% of the highest dose using the original/birth weight (same amount each time) every 24 to 48 hours, provided the scores remain below 8.

  • Morphine SulfateDrug

    Also called Morphine

    Morphine at 0.03 mg/kg/dose every 3 hours or 0.04 mg/kg/dose every 4 hours Morphine dose will be increased by 25% of the previous dose if needed. It will be decreased by 10% of the highest dose using the original/birth weight (same amount each time) every 24 to 48 hours, provided the scores remain below 8.

Study groups in NCT03092011
Study groupRoleWhat they receive
ClonidineExperimentalClonidine at 0.38 mcg/kg/dose every 3 hours or 0.5 mcg/kg/dose every 4 hours
Receives: Drug: Clonidine
MorphineActive comparatorMorphine Sulfate at 0.03 mg/kg/dose every 3 hours or 0.04 mg/kg/dose every 4 hours
Receives: Drug: Morphine Sulfate

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Length of treatment

    Duration of treatment of Neonatal Abstinence Syndrome with medication/pharmacological treatment from first day initiated until medication has been stopped or patient discharged home

    Measured: From initiation of medical treatment through last dose of medication given, up to 100 days

Secondary outcomes (1)
  1. Length of stay

    Duration of hospitalization

    Measured: From birth through discharge from the hospital, up to 100 days.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Mar 2017
  2. Study start21 Feb 2018
  3. Primary completion1 Oct 2024
  4. Study completion1 Dec 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Randomized double blind prospective trial
Masking
Double blind
Who is masked
Participant, Care provider
Enrolment
69 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03092011
Sponsor's protocol ID
16-144
Status last verified
Oct 2024
First submitted
13 Mar 2017
Last updated
15 Oct 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
No

Publications

  • Zankl A, Martin J, Davey JG, Osborn DA. Opioid treatment for opioid withdrawal in newborn infants. Cochrane Database Syst Rev. 2021 Jul 7;7(7):CD002059. doi: 10.1002/14651858.CD002059.pub4.

    PubMed 34231914

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Clonidine and Morphine Sulfate in people with Neonatal Abstinence Syndrome, run by Cooper Norcross Health at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: under way, not looking for participants, as of the sponsor's last update on 15 Oct 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Length of treatment (time frame: From initiation of medical treatment through last dose of medication given, up to 100 days). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT03092011, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Oct 2024.

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