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Sponsored by: |
University of Johannesburg |
Information provided by: | University of Johannesburg |
ClinicalTrials.gov Identifier: | NCT00204139 |
It is debatable whether routine ultrasound scanning of pregnancies at about 20 weeks of pregnancy has substantive benefits for mothers and babies. Few studies have addressed this issue in poorly resourced settings. This trial will attempt to determine the benefits, if any, of a policy of routine ultrasound scanning of normal pregnancies versus a policy of no routine (only selective) scanning. This will be done by recruiting about 900 women in South Africa, and randomly allocating about half to routine scanning and half to selective scanning groups, and following up their pregnancies.
Condition | Intervention | Phase |
Fetal Congenital Abnormalities Prolonged Pregnancy Multiple Pregnancy |
Procedure: Routine midtrimester pregnany ultrasound scan |
Phase III |
MedlinePlus related topics: | Nuclear Scans Ultrasound |
Study Type: | Interventional |
Study Design: | Diagnostic, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study |
Estimated Enrollment: | 900 |
Study Start Date: | June 2002 |
Estimated Study Completion Date: | May 2004 |
Routine ultrasound scanning in the second trimester of pregnancy has few substantive benefits, according to the results of number of randomised trials, mostly performed in industrialised countries. While ultrasound did not seem to prevent fetal death, it was associated with improved detection of multiple pregnancies, improved detection of congenital abnormalities and reduced need for postterm labour induction. Only one trial, from Cape Town, has investigated the benefits of a policy of routine second trimester ultrasound scanning in an under-resourced setting.
This will be cluster randomised controlled trial, performed in the Krugersdorp area of South Africa, where most health service users are African, working class and dependent on government health facilities. About 900 low-risk pregnant women at less than 24 weeks gestation will be recruited, and randomised, in clusters, to either routine scanning or no scanning with recourse to selective scanning if clinically indicated.
Women will be followed up for maternal, fetal and neonatal outcome, and for indices of health service utilisation. Important outcome measures will be need for subsequent ultrasound,detection of multiple pregnancy, detection of congenital abnormalities, postterm pregnancy induction, still birth,and neonatal morbidity and mortality.
Data analysis will compare outcomes according to whether routine ultrasound scanning was or was not done, using standard statistical methods.
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Female |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
South Africa, Gauteng | |||||
University of Johannesburg | |||||
Johannesburg, Gauteng, South Africa, 2000 |
University of Johannesburg |
Study Chair: | Eckhart J Buchmann, MBBCh | University of the Witwatersrand, Johannesburg |
Study ID Numbers: | BvanDyk USS |
First Received: | September 12, 2005 |
Last Updated: | September 12, 2005 |
ClinicalTrials.gov Identifier: | NCT00204139 |
Health Authority: | South Africa: National Health Research Ethics Council |
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