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RCT Comparing Methadone and Buprenorphine in Pregnant Women

Primary Purpose

Opioid Related Disorders, Pregnancy, Opioid Dependence

Status
Completed
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
Methadone
Buprenorphine
Sponsored by
Johns Hopkins University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Opioid Related Disorders focused on measuring opiate addiction, opiate dependence, substance abuse, addiction, substance addiction, pregnancy, buprenorphine, methadone, fetal, neonatal, post-partum

Eligibility Criteria

18 Years - 41 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria: Current opioid dependence Current opioid use, as determined by a urine drug test Pregnant with a single child with a gestational age of 6 to 30 weeks, as determined by a sonogram Exclusion Criteria: Current medical condition that would make study participation dangerous, as determined by study physician Diagnosed with an acute, severe psychiatric illness Current SCID I-E module diagnosis of benzodiazepine or alcohol abuse Use of alcohol or benzodiazepines in the 30 days prior to study entry, as determined by the Addiction Severity Index Pending legal action that may prohibit or interfere with study participation

Sites / Locations

  • Johns Hopkins University School of Medicine
  • Wayne State University
  • Thomas Jefferson University
  • Brown University
  • Vanderbilt University
  • University of Vermont
  • Medical University of Vienna
  • St. Joseph's Health Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Buprenorphine

Methadone

Arm Description

Buprenorphine

Methadone

Outcomes

Primary Outcome Measures

Child's Head Circumference Measurement (Measured at Birth)
Child's Length of Hospital Stay
Number of Children Requiring Treatment for Neonatal Abstinence Signs (NAS)
Neonatal abstinence syndrome (NAS) characterized by hyperirritability of the central nervous system and dysfunction in the autonomic nervous system, gastrointestinal tract, and respiratory system.11 When left untreated, NAS can result in serious illness (e.g., diarrhea, feeding difficulties, weight loss, and seizures) and death.
Child's Peak Daily Total NAS Score
NAS was measured with the MOTHER NAS scale, which includes 28 items, 19 of which are used for scoring and medication decisions. Scores can range from 0 to 42, with higher scores indicating more severe withdrawal.
Total Amount of Morphine Sulfate That a Neonate Receives to Treat NAS
Total amount in mg

Secondary Outcome Measures

Mother's Self-report of Drug Use (Measured Monthly by Time Line Follow Back)
Mother's HIV Risk Behaviors (Measured Monthly by Risk Behavior Assessment)
Mother's Measures of Dose Adequacy and Acceptance Over Time (Measured Weekly by Dose Adequacy Measure)
Pregnant women maintained on an opioid agonist medication may require upward adjustment to their medication during the course of pregnant. The Dose Adequacy Measure represented a recordation of dosing adjustments during the course of the study.
Mother's Psychosocial Functioning at Delivery as Measured by the Addiction Severity Index Psychosocial Index Score
The Addiction Severity Index is a structured clinical interview that assesses problem severity in 7 areas of functioning: alcohol use, drug use, medical, legal, employment, psychosocial, and psychiatric status. Each area of functioning yields a composite scale score between 0 and 1, with higher scores indicating greater problem severity in that area. Only the psychosocial index was examined in this study.

Full Information

First Posted
December 28, 2005
Last Updated
July 30, 2015
Sponsor
Johns Hopkins University
Collaborators
National Institute on Drug Abuse (NIDA)
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1. Study Identification

Unique Protocol Identification Number
NCT00271219
Brief Title
RCT Comparing Methadone and Buprenorphine in Pregnant Women
Official Title
Maternal Opioid Treatment: Human Experimental Research
Study Type
Interventional

2. Study Status

Record Verification Date
July 2015
Overall Recruitment Status
Completed
Study Start Date
July 2005 (undefined)
Primary Completion Date
August 2009 (Actual)
Study Completion Date
June 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Johns Hopkins University
Collaborators
National Institute on Drug Abuse (NIDA)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Children born to women who abuse drugs have a high risk of being born with birth defects and developmental problems. Methadone is a drug that is commonly used for treating opioid dependence. However, its use by a pregnant woman can cause severe withdrawal symptoms in a newborn because of the prenatal exposure. The purpose of this study is to evaluate the effectiveness of buprenorphine, another drug, versus methadone in reducing withdrawal symptoms in children born to opioid-dependent women.
Detailed Description
Women who use drugs during pregnancy place their unborn children at high risk for being born addicted to drugs. Such children may also be born with birth defects and may experience learning and behavioral problems. Methadone, a synthetic narcotic, is commonly prescribed to treat opioid addiction. It may not be an optimal solution for opioid-dependent pregnant women, however, because a large percentage of children born to women taking methadone experience severe drug withdrawal symptoms at birth that often require medical treatment. Common opioid withdrawal symptoms, described as neonatal abstinence syndrome (NAS) in babies, include tremors, irritability, sleep problems, seizures, dehydration, and fever. Buprenorphine is a medication that has been approved to treat opioid dependence in individuals who are not pregnant but has not been approved for pregnant individuals. Past research has shown that use of buprenorphine in pregnant women results in improved birth outcomes over methadone. The purpose of this study is to evaluate the effectiveness of buprenorphine versus methadone at reducing opioid withdrawal symptoms in babies born to opioid-dependent women. This study will enroll opioid-dependent pregnant women who are 13 to 30 weeks pregnant and will follow each woman and her child throughout the pregnancy until 6 weeks postpartum. All participants will undergo an initial screening that will last several hours. Participants will then be randomly assigned to receive either methadone or buprenorphine on a daily basis, and will be required to visit the clinic each day to receive their medication. Outcome measurements will be assessed at weekly study visits throughout the pregnancy, and will include drug use, HIV risk behaviors, medication dose adequacy and safety, treatment retention, and psychosocial functioning. Urine samples will be collected 3 times a week, and blood will be drawn throughout the pregnancy for safety monitoring. Outcome measurements related to the baby will include head circumference measurement, length of hospital stay, severity and frequency of withdrawal symptoms, and amount of medication needed to control withdrawal symptoms.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Opioid Related Disorders, Pregnancy, Opioid Dependence
Keywords
opiate addiction, opiate dependence, substance abuse, addiction, substance addiction, pregnancy, buprenorphine, methadone, fetal, neonatal, post-partum

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
175 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Buprenorphine
Arm Type
Experimental
Arm Description
Buprenorphine
Arm Title
Methadone
Arm Type
Active Comparator
Arm Description
Methadone
Intervention Type
Drug
Intervention Name(s)
Methadone
Intervention Description
daily oral dosing 20-140 mg
Intervention Type
Drug
Intervention Name(s)
Buprenorphine
Intervention Description
sl daily 2-32 mg
Primary Outcome Measure Information:
Title
Child's Head Circumference Measurement (Measured at Birth)
Time Frame
birth
Title
Child's Length of Hospital Stay
Time Frame
delivery until hospital discharge (min=2 days, max=79 days)
Title
Number of Children Requiring Treatment for Neonatal Abstinence Signs (NAS)
Description
Neonatal abstinence syndrome (NAS) characterized by hyperirritability of the central nervous system and dysfunction in the autonomic nervous system, gastrointestinal tract, and respiratory system.11 When left untreated, NAS can result in serious illness (e.g., diarrhea, feeding difficulties, weight loss, and seizures) and death.
Time Frame
From birth until hospital discharge (min=4 days, max=10, depending on site)
Title
Child's Peak Daily Total NAS Score
Description
NAS was measured with the MOTHER NAS scale, which includes 28 items, 19 of which are used for scoring and medication decisions. Scores can range from 0 to 42, with higher scores indicating more severe withdrawal.
Time Frame
minimum twice daily from birth until NAS no longer measured (min=10 days)
Title
Total Amount of Morphine Sulfate That a Neonate Receives to Treat NAS
Description
Total amount in mg
Time Frame
Start of NAS treatment until discontinuation of NAS treatment (min=0 days, max=76 days)
Secondary Outcome Measure Information:
Title
Mother's Self-report of Drug Use (Measured Monthly by Time Line Follow Back)
Time Frame
monthly from study entry until discontinuation or delivery (min=29 days, max=239 days)
Title
Mother's HIV Risk Behaviors (Measured Monthly by Risk Behavior Assessment)
Time Frame
monthly from study entry until discontinuation or delivery (min=29 days, max=239 days)
Title
Mother's Measures of Dose Adequacy and Acceptance Over Time (Measured Weekly by Dose Adequacy Measure)
Description
Pregnant women maintained on an opioid agonist medication may require upward adjustment to their medication during the course of pregnant. The Dose Adequacy Measure represented a recordation of dosing adjustments during the course of the study.
Time Frame
from study entry until discontinuation or delivery (min=29 days, max=239 days)
Title
Mother's Psychosocial Functioning at Delivery as Measured by the Addiction Severity Index Psychosocial Index Score
Description
The Addiction Severity Index is a structured clinical interview that assesses problem severity in 7 areas of functioning: alcohol use, drug use, medical, legal, employment, psychosocial, and psychiatric status. Each area of functioning yields a composite scale score between 0 and 1, with higher scores indicating greater problem severity in that area. Only the psychosocial index was examined in this study.
Time Frame
at delivery

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
41 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Current opioid dependence Current opioid use, as determined by a urine drug test Pregnant with a single child with a gestational age of 6 to 30 weeks, as determined by a sonogram Exclusion Criteria: Current medical condition that would make study participation dangerous, as determined by study physician Diagnosed with an acute, severe psychiatric illness Current SCID I-E module diagnosis of benzodiazepine or alcohol abuse Use of alcohol or benzodiazepines in the 30 days prior to study entry, as determined by the Addiction Severity Index Pending legal action that may prohibit or interfere with study participation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hendree E. Jones, PhD
Organizational Affiliation
Johns Hopkins University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Johns Hopkins University School of Medicine
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21224
Country
United States
Facility Name
Wayne State University
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48207
Country
United States
Facility Name
Thomas Jefferson University
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19107
Country
United States
Facility Name
Brown University
City
Providence
State/Province
Rhode Island
ZIP/Postal Code
02912
Country
United States
Facility Name
Vanderbilt University
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37232
Country
United States
Facility Name
University of Vermont
City
Burlington
State/Province
Vermont
ZIP/Postal Code
05401
Country
United States
Facility Name
Medical University of Vienna
City
Vienna
ZIP/Postal Code
A1090
Country
Austria
Facility Name
St. Joseph's Health Centre
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M6R 1B5
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
23786504
Citation
Jones HE, Kaltenbach K, Heil SH, Stine SM, Coyle MG, Arria AM, O'Grady KE, Selby P, Martin PR. Nonserious adverse events in randomized trials with opioid-dependent pregnant women: direct versus indirect measurement. Am J Addict. 2012 Nov;21 Suppl 1:S1-4. doi: 10.1111/j.1521-0391.2012.00289.x.
Results Reference
derived
PubMed Identifier
23523131
Citation
Holbrook AM, Jones HE, Heil SH, Martin PR, Stine SM, Fischer G, Coyle MG, Kaltenbach K. Induction of pregnant women onto opioid-agonist maintenance medication: an analysis of withdrawal symptoms and study retention. Drug Alcohol Depend. 2013 Sep 1;132(1-2):329-34. doi: 10.1016/j.drugalcdep.2013.02.031. Epub 2013 Mar 21.
Results Reference
derived
PubMed Identifier
23279924
Citation
Jones HE, Heil SH, Tuten M, Chisolm MS, Foster JM, O'Grady KE, Kaltenbach K. Cigarette smoking in opioid-dependent pregnant women: neonatal and maternal outcomes. Drug Alcohol Depend. 2013 Aug 1;131(3):271-7. doi: 10.1016/j.drugalcdep.2012.11.019. Epub 2012 Dec 29.
Results Reference
derived
PubMed Identifier
23106931
Citation
McNicholas LF, Holbrook AM, O'Grady KE, Jones HE, Coyle MG, Martin PR, Heil SH, Stine SM, Kaltenbach K. Effect of hepatitis C virus status on liver enzymes in opioid-dependent pregnant women maintained on opioid-agonist medication. Addiction. 2012 Nov;107 Suppl 1(0 1):91-7. doi: 10.1111/j.1360-0443.2012.04043.x.
Results Reference
derived
PubMed Identifier
23106930
Citation
Holbrook AM, Baxter JK, Jones HE, Heil SH, Coyle MG, Martin PR, Stine SM, Kaltenbach K. Infections and obstetric outcomes in opioid-dependent pregnant women maintained on methadone or buprenorphine. Addiction. 2012 Nov;107 Suppl 1(Suppl 1):83-90. doi: 10.1111/j.1360-0443.2012.04042.x.
Results Reference
derived
PubMed Identifier
23106929
Citation
Benningfield MM, Dietrich MS, Jones HE, Kaltenbach K, Heil SH, Stine SM, Coyle MG, Arria AM, O'Grady KE, Fischer G, Martin PR. Opioid dependence during pregnancy: relationships of anxiety and depression symptoms to treatment outcomes. Addiction. 2012 Nov;107 Suppl 1(0 1):74-82. doi: 10.1111/j.1360-0443.2012.04041.x.
Results Reference
derived
PubMed Identifier
23106928
Citation
Coyle MG, Salisbury AL, Lester BM, Jones HE, Lin H, Graf-Rohrmeister K, Fischer G. Neonatal neurobehavior effects following buprenorphine versus methadone exposure. Addiction. 2012 Nov;107 Suppl 1(0 1):63-73. doi: 10.1111/j.1360-0443.2012.04040.x.
Results Reference
derived
PubMed Identifier
23106927
Citation
Gaalema DE, Scott TL, Heil SH, Coyle MG, Kaltenbach K, Badger GJ, Arria AM, Stine SM, Martin PR, Jones HE. Differences in the profile of neonatal abstinence syndrome signs in methadone- versus buprenorphine-exposed neonates. Addiction. 2012 Nov;107 Suppl 1(0 1):53-62. doi: 10.1111/j.1360-0443.2012.04039.x.
Results Reference
derived
PubMed Identifier
23106926
Citation
Kaltenbach K, Holbrook AM, Coyle MG, Heil SH, Salisbury AL, Stine SM, Martin PR, Jones HE. Predicting treatment for neonatal abstinence syndrome in infants born to women maintained on opioid agonist medication. Addiction. 2012 Nov;107 Suppl 1(0 1):45-52. doi: 10.1111/j.1360-0443.2012.04038.x.
Results Reference
derived
PubMed Identifier
23106925
Citation
Salisbury AL, Coyle MG, O'Grady KE, Heil SH, Martin PR, Stine SM, Kaltenbach K, Weninger M, Jones HE. Fetal assessment before and after dosing with buprenorphine or methadone. Addiction. 2012 Nov;107 Suppl 1(0 1):36-44. doi: 10.1111/j.1360-0443.2012.04037.x.
Results Reference
derived
PubMed Identifier
23106924
Citation
Jones HE, Fischer G, Heil SH, Kaltenbach K, Martin PR, Coyle MG, Selby P, Stine SM, O'Grady KE, Arria AM. Maternal Opioid Treatment: Human Experimental Research (MOTHER)--approach, issues and lessons learned. Addiction. 2012 Nov;107 Suppl 1(0 1):28-35. doi: 10.1111/j.1360-0443.2012.04036.x.
Results Reference
derived
PubMed Identifier
23106923
Citation
Jones HE, Heil SH, Baewert A, Arria AM, Kaltenbach K, Martin PR, Coyle MG, Selby P, Stine SM, Fischer G. Buprenorphine treatment of opioid-dependent pregnant women: a comprehensive review. Addiction. 2012 Nov;107 Suppl 1(0 1):5-27. doi: 10.1111/j.1360-0443.2012.04035.x.
Results Reference
derived
PubMed Identifier
22088886
Citation
Unger A, Jagsch R, Bawert A, Winklbaur B, Rohrmeister K, Martin PR, Coyle M, Fischer G. Are male neonates more vulnerable to neonatal abstinence syndrome than female neonates? Gend Med. 2011 Dec;8(6):355-64. doi: 10.1016/j.genm.2011.10.001. Epub 2011 Nov 15.
Results Reference
derived
PubMed Identifier
21142534
Citation
Jones HE, Kaltenbach K, Heil SH, Stine SM, Coyle MG, Arria AM, O'Grady KE, Selby P, Martin PR, Fischer G. Neonatal abstinence syndrome after methadone or buprenorphine exposure. N Engl J Med. 2010 Dec 9;363(24):2320-31. doi: 10.1056/NEJMoa1005359.
Results Reference
derived

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RCT Comparing Methadone and Buprenorphine in Pregnant Women

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