Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE4
21780 participants
INTERVENTIONAL
2003-09-30
2006-12-31
Brief Summary
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Detailed Description
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Following baseline data collections in 24 hospitals, 19 hospitals met inclusion criteria in three urban districts of Argentina and Uruguay and were randomly assigned to an intervention or control group. Baseline data collection has been completed with a total of 6597 single vaginal spontaneous births. The 19 hospitals met inclusion criteria with a rate of active management of third stage of labor under 25% and an episiotomy rate in spontaneous vaginal deliveries above 20%. Opinion leaders in the intervention hospitals have been identified and trained to develop evidence-based guidelines that will be diffused by a multifaceted approach including seminars, academic detailing, reminders, and feedback on utilization rates. The hospitals in the nonintervention group will continue with their standard in-service training activities.
Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
NONE
Interventions
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Opinion Leaders, Academic Detailing, Reminders, and Feedback
Eligibility Criteria
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Inclusion Criteria
* have an Institutional Review Board (IRB), or existing committee which could serve as such, or have an agreement with an IRB which reviews the research protocols implemented in the hospital;
* have at least 500 vaginal deliveries per year;
* do not have an explicit policy for selective episiotomy and for active management of third stage of labor;
* are located within the study area in Argentina and Uruguay; and
* agree to participate in the study.
Exclusion Criteria
* Episiotomy rate in spontaneous vaginal deliveries below 20%
* Rate of active management of third stage of labor over 25%
The sample size of the study was increased to allow for exclusions.
Expectant management is defined as "a hands-free policy" during third stage of labor until the placenta is expelled: no use of uterotonics or special maneuvers.
Sampling, Recruitment, and Screening Procedures
Latin American Center for Perinatology (CLAP) coordination team will be responsible for the hospital selection. The hospitals' fulfillment of selection criteria will be obtained through a survey of the Heads of the Obstetrical Departments.
Besides the selection criteria, the coordination unit will invite the hospitals to participate according to:
* their participation in previous trials coordinated by CLAP,
* their participation in other trials or research activities, and
* their location.
Of particular interest are the characteristics of each preselected hospital regarding the structure of the professional staff, number of deliveries, and clinical guidelines policy.
ALL
No
Sponsors
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Global Network for Women's and Children's Health Research
OTHER
Bill and Melinda Gates Foundation
OTHER
Fogarty International Center of the National Institute of Health
NIH
National Center for Complementary and Integrative Health (NCCIH)
NIH
National Institute of Dental and Craniofacial Research (NIDCR)
NIH
National Cancer Institute (NCI)
NIH
RTI International
OTHER
Latin American Center for Perinatology
OTHER
Pan American Health Organization
OTHER
World Health Organization
OTHER
Tulane University School of Public Health and Tropical Medicine
OTHER
University of North Carolina, Chapel Hill
OTHER
NICHD Global Network for Women's and Children's Health
NETWORK
Responsible Party
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Principal Investigators
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Pierre Buekens, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Tulane School of Public Health and Tropical Medicine
Locations
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Hospital de Clinicas
Montevideo, , Uruguay
Countries
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References
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Althabe F, Buekens P, Bergel E, Belizan JM, Kropp N, Wright L, Goco N, Moss N; for the Guidelines Trial Group. A cluster randomized controlled trial of a behavioral intervention to facilitate the development and implementation of clinical practice guidelines in Latin American maternity hospitals: the Guidelines Trial: Study protocol [ISRCTN82417627]. BMC Womens Health. 2005 Apr 11;5(1):4. doi: 10.1186/1472-6874-5-4.
Kropp N, Hartwell T, Althabe F. Episiotomy rates from eleven developing countries. Int J Gynaecol Obstet. 2005 Nov;91(2):157-9. doi: 10.1016/j.ijgo.2005.07.013. Epub 2005 Oct 5. No abstract available.
Althabe F, Buekens P, Bergel E, Belizan JM, Campbell MK, Moss N, Hartwell T, Wright LL; Guidelines Trial Group. A behavioral intervention to improve obstetrical care. N Engl J Med. 2008 May 1;358(18):1929-40. doi: 10.1056/NEJMsa071456.
Related Links
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Tulane School of Public Health and Tropical Medicine
RTI International
Institute for Clinical Effectiveness and Health Policy (IECS)
Other Identifiers
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GN 01
Identifier Type: -
Identifier Source: org_study_id