Trial of the Use of Antenatal Corticosteroids in Developing Countries (ACT)
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Purpose
Multi-country two-arm, parallel cluster randomized controlled trial to reduce neonatal mortality through increasing the rate of antenatal corticosteroid administration to eligible women.
| Condition | Intervention | Phase |
|---|---|---|
|
Preterm Birth |
Behavioral: Increasing use of Antenatal Corticosteroids (ACS) |
Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Trial of the Use of Antenatal Corticosteroids in Developing Countries |
- Neonatal mortality at 28 days in low birth weight infants (as a proxy measure for prematurity) [ Time Frame: 28 days ] [ Designated as safety issue: No ]
- Use of antenatal corticosteroids in women at risk of preterm birth in all the study clusters [ Time Frame: 48 hours after identification of risk for preterm birth ] [ Designated as safety issue: No ]Antenatal corticosteroid use will be assessed in all LBW newborn infants, defined as the number of live-born babies in predefined birth weight groups whose mothers received at least one 6-mg antenatal dose of dexamethasone for prevention of neonatal complications, per 1000 live-birth babies born in the same birth weight group.
| Estimated Enrollment: | 6000 |
| Study Start Date: | October 2011 |
| Estimated Study Completion Date: | January 2014 |
| Estimated Primary Completion Date: | January 2014 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: Intervention
Eligible women at high risk for preterm birth will be identified and four 6 mg doses of dexamethasone will be administered before delivery.
|
Behavioral: Increasing use of Antenatal Corticosteroids (ACS)
Intervention clusters:
Control clusters: no specific intervention for comparison. Both intervention and control clusters: Birth attendants trained in essential newborn care of LBW infants and instructed to teach mothers how to provide care to premature infants. |
|
No Intervention: Control
Control arm will not receive a specific intervention for comparison.
|
Detailed Description:
One of the United Nations Millennium Summit goals is to reduce the deaths of children <5 years by two-thirds for 2015 (UN, 2000). Given that 38% of all under-five deaths worldwide occur in the first four weeks of life, the goal seems unattainable unless a significant fraction of the neonatal deaths are prevented (Darmstadt et al., 2005). Thus, the provision of health care during the perinatal period in developing countries is a top priority. Preterm birth is a major cause of neonatal mortality, currently responsible for 28% of the deaths overall. As the contribution of preterm birth to neonatal deaths is well above 50% (MacDorman et al., 2005) in middle and high income countries, it is expected that as low income countries improve their development, the relative importance of this cause will increase. One of the most powerful perinatal interventions to reduce neonatal mortality is the administration of antenatal corticosteroids to pregnant women at high risk of preterm birth.
The primary objective will be to evaluate whether a cluster-level multifaceted intervention, including components to improve the identification of pregnancies at high risk of preterm birth and providing and facilitating the appropriate use of steroids, reduces neonatal mortality at 28 days of life in preterm newborns, compared with the standard delivery of care in selected populations of six African, Asian, and Latin American countries.
Eligibility| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | Yes |
This is an intent-to-treat design and thus all pregnancy outcomes of women who deliver in the study clusters and provide consent will be collected. Cluster-level inclusion criteria include
- At least 250 deliveries per year.
- Birth attendants within the health cluster will be consented to participate
Participant-level inclusion criteria include all pregnant women living in and delivering in the study cluster who:
- Are between 24 and 36 weeks GA;
- Present with signs of preterm labor, amniotic fluid leakage, hemorrhage, or hypertension;
- Provide consent for injection or present to a facility where it is standard of care.
Exclusion Criteria:
- There will not be any specific exclusion criteria for clusters or participants.
Contacts and Locations| Contact: Marion Koso-Thomas, MD | 301-435-6873 | kosomari@mail.nih.gov |
| Contact: Linda Wright, MD | 301-402-0830 | wrightl@mail.nih.gov |
| Argentina | |
| Institute for Clinical Effectiveness and Health Policy (IECS) | Recruiting |
| Buenos Aires, Argentina | |
| Contact: Fernando Althabe, MD +5411 47778767 ext 17 althabef@gmail.com | |
| Contact: Jose Belizan, MD +5411 47778767 ext 17 belizanj@gmail.com | |
| Guatemala | |
| Universidad Francisco Marroquin Facultad de Medicina | Recruiting |
| Guatemala City, Guatemala | |
| Contact: Ana Garces, MD +502-2332-4064 anagarces@imsalud.org | |
| India | |
| JN Medical College | Recruiting |
| Belgaum, India | |
| Contact: Bhala Kodkany, MD +91 831 2409 2051 drkodkany@jnmc.edu | |
| Lata Medical Research Foundation | Recruiting |
| Nagpur, India | |
| Contact: Archana Patel, MD 91-98 2315 4463 dr_apatel@yahoo.com | |
| Kenya | |
| Moi University School of Medicine | Recruiting |
| Eldoret, Kenya | |
| Contact: Fabian Esamai, MD (254) 733 836 410 fesamai2007@gmail.com | |
| Pakistan | |
| Aga Khan University | Recruiting |
| Karachi, Pakistan | |
| Contact: Omrana Pasha, MD (92-21) 3486-4948 omrana.pasha@aku.edu | |
| Zambia | |
| University of Zambia | Recruiting |
| Lusaka, Zambia | |
| Contact: Elwyn Chomba, MD +260211 254655 echomba@zamnet.zm | |
| Principal Investigator: | Fernando Althabe, M.D. | Institute for Clinical Effectiveness and Health Policy (IECS), Buenos Aires, Argentina |
More Information
No publications provided by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) |
| ClinicalTrials.gov Identifier: | NCT01084096 History of Changes |
| Other Study ID Numbers: | GN ACT Study |
| Study First Received: | March 9, 2010 |
| Last Updated: | August 30, 2012 |
| Health Authority: | United States: Federal Government |
Keywords provided by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD):
|
Antenatal Corticosteroids, Preterm Birth, Diffusion |
Additional relevant MeSH terms:
|
Premature Birth Obstetric Labor, Premature Obstetric Labor Complications Pregnancy Complications |
ClinicalTrials.gov processed this record on May 21, 2013