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RCT Comparing Methadone and Buprenorphine in Pregnant Women

2015년 7월 30일 업데이트: Hendree E. Jones, Johns Hopkins University

Maternal Opioid Treatment: Human Experimental Research

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.

연구 개요

상세 설명

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.

연구 유형

중재적

등록 (실제)

175

단계

  • 3단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

    • Maryland
      • Baltimore, Maryland, 미국, 21224
        • Johns Hopkins University School of Medicine
    • Michigan
      • Detroit, Michigan, 미국, 48207
        • Wayne State University
    • Pennsylvania
      • Philadelphia, Pennsylvania, 미국, 19107
        • Thomas Jefferson University
    • Rhode Island
      • Providence, Rhode Island, 미국, 02912
        • Brown University
    • Tennessee
      • Nashville, Tennessee, 미국, 37232
        • Vanderbilt University
    • Vermont
      • Burlington, Vermont, 미국, 05401
        • University of Vermont
      • Vienna, 오스트리아, A1090
        • Medical University of Vienna
    • Ontario
      • Toronto, Ontario, 캐나다, M6R 1B5
        • St. Joseph's Health Centre

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 (성인)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

여성

설명

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

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 네 배로

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: 부프레노르핀
sl daily 2-32 mg
활성 비교기: Methadone
daily oral dosing 20-140 mg

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Child's Head Circumference Measurement (Measured at Birth)
기간: birth
birth
Child's Length of Hospital Stay
기간: delivery until hospital discharge (min=2 days, max=79 days)
delivery until hospital discharge (min=2 days, max=79 days)
Number of Children Requiring Treatment for Neonatal Abstinence Signs (NAS)
기간: From birth until hospital discharge (min=4 days, max=10, depending on site)
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.
From birth until hospital discharge (min=4 days, max=10, depending on site)
Child's Peak Daily Total NAS Score
기간: minimum twice daily from birth until NAS no longer measured (min=10 days)
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.
minimum twice daily from birth until NAS no longer measured (min=10 days)
Total Amount of Morphine Sulfate That a Neonate Receives to Treat NAS
기간: Start of NAS treatment until discontinuation of NAS treatment (min=0 days, max=76 days)
Total amount in mg
Start of NAS treatment until discontinuation of NAS treatment (min=0 days, max=76 days)

2차 결과 측정

결과 측정
측정값 설명
기간
Mother's Self-report of Drug Use (Measured Monthly by Time Line Follow Back)
기간: monthly from study entry until discontinuation or delivery (min=29 days, max=239 days)
monthly from study entry until discontinuation or delivery (min=29 days, max=239 days)
Mother's HIV Risk Behaviors (Measured Monthly by Risk Behavior Assessment)
기간: monthly from study entry until discontinuation or delivery (min=29 days, max=239 days)
monthly from study entry until discontinuation or delivery (min=29 days, max=239 days)
Mother's Measures of Dose Adequacy and Acceptance Over Time (Measured Weekly by Dose Adequacy Measure)
기간: from study entry until discontinuation or delivery (min=29 days, max=239 days)
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.
from study entry until discontinuation or delivery (min=29 days, max=239 days)
Mother's Psychosocial Functioning at Delivery as Measured by the Addiction Severity Index Psychosocial Index Score
기간: at delivery
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.
at delivery

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: Hendree E. Jones, PhD, Johns Hopkins University

간행물 및 유용한 링크

연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.

일반 간행물

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작

2005년 7월 1일

기본 완료 (실제)

2009년 8월 1일

연구 완료 (실제)

2010년 6월 1일

연구 등록 날짜

최초 제출

2005년 12월 28일

QC 기준을 충족하는 최초 제출

2005년 12월 28일

처음 게시됨 (추정)

2005년 12월 30일

연구 기록 업데이트

마지막 업데이트 게시됨 (추정)

2015년 8월 5일

QC 기준을 충족하는 마지막 업데이트 제출

2015년 7월 30일

마지막으로 확인됨

2015년 7월 1일

추가 정보

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

임신에 대한 임상 시험

Buprenorphine에 대한 임상 시험

3
구독하다