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Improving Perinatal Care in Latin America

Clustered Trial for Improving Perinatal Care in Uruguay/Argentina

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00070720
Enrollment
21780
Registered
2003-10-13
Start date
2003-09-30
Completion date
2006-12-31
Last updated
2013-12-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Episiotomy, Pregnancy

Keywords

Behavior change, Change in practitioner behavior, Episiotomy, Active management of third stage of labor, Global Network, Latin America, Uruguay, Argentina, Maternal and child health, International, Women's health

Brief summary

Many obstetrical interventions used in Latin America, as in other parts of the world, have been shown to be ineffective or harmful, while effective interventions remain underutilized. This study will develop and evaluate an intervention intended to implement two evidence-based practices among birth attendants in Latin America, the selective use of episiotomies and active management of the third stage of labor.

Detailed description

In Latin American countries certain procedures commonly used in obstetrical care (e.g. episiotomy) have been shown to be ineffective or harmful. This study hypothesizes that obstetrical procedures can be changed and new guidelines implemented via peer opinion leader training. It tests an intervention designed to motivate and facilitate health care professionals' development through the implementation and maintenance of simple evidence-based guidelines to increase the use of evidence-based practices by birth attendants at the hospital level in Argentina and Uruguay. The primary outcomes are the use of episiotomies and of oxytocin during the third stage of labor; secondary outcomes include perineal sutures; postpartum hemorrhages; birth attendants' readiness to change status. The sample size was based upon a 10% frequency of oxytocin use and 20% use of episiotomies in the control group. The study hypothesizes a 40% absolute increase in oxytocin use in the intervention group; a 20% absolute reduction in use of episiotomies in the intervention group, calculated at a 0.05 significance level with 80% power. 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.

Interventions

BEHAVIORALOpinion Leaders, Academic Detailing, Reminders, and Feedback

Sponsors

Global Network for Women's and Children's Health Research
CollaboratorOTHER
Bill and Melinda Gates Foundation
CollaboratorOTHER
Fogarty International Center of the National Institute of Health
CollaboratorNIH
National Center for Complementary and Integrative Health (NCCIH)
CollaboratorNIH
National Institute of Dental and Craniofacial Research (NIDCR)
CollaboratorNIH
National Cancer Institute (NCI)
CollaboratorNIH
RTI International
CollaboratorOTHER
Latin American Center for Perinatology
CollaboratorOTHER
Pan American Health Organization
CollaboratorOTHER
World Health Organization
CollaboratorOTHER
Tulane University School of Public Health and Tropical Medicine
CollaboratorOTHER
University of North Carolina, Chapel Hill
CollaboratorOTHER
NICHD Global Network for Women's and Children's Health
Lead SponsorNETWORK

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

for Hospitals Hospitals were invited to participate in the study if they fulfill the following 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

for Hospitals Preselected hospitals are performing baseline data collection. According to the results of the analysis of the baseline data collection, hospitals will be excluded if the episiotomy rate is low or the rate of active management of the third stage of labor is high, according to the following cut-off points: * 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.

Design outcomes

Primary

MeasureTime frame
Episiotomies
Oxytocin use in third stage of labor

Secondary

MeasureTime frame
Perineal sutures
Postpartum hemorrhage
Birth attendants' readiness to change status

Countries

Uruguay

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 5, 2026