search
Back to results

Routine Versus Selective Midtrimester Ultrasound in a Poorly Resourced Setting: a Cluster Randomised Controlled Trial

Primary Purpose

Fetal Congenital Abnormalities, Prolonged Pregnancy, Multiple Pregnancy

Status
Completed
Phase
Phase 3
Locations
South Africa
Study Type
Interventional
Intervention
Routine midtrimester pregnany ultrasound scan
Sponsored by
University of Johannesburg
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Fetal Congenital Abnormalities

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria: Pregnancy, 24 weeks pregnant or less, willing to participate Exclusion Criteria: High risk pregnancy condition, e.g. poor past obstetric history, hypertensive disease, previous caesarean section

Sites / Locations

  • University of Johannesburg

Outcomes

Primary Outcome Measures

Detection of congenital abnormalities
Postterm pregnancy inductions

Secondary Outcome Measures

Detection of multiple pregnancies
Stillbirths
Neonatal morbidity
Neonatal mortality

Full Information

First Posted
September 12, 2005
Last Updated
September 12, 2005
Sponsor
University of Johannesburg
search

1. Study Identification

Unique Protocol Identification Number
NCT00204139
Brief Title
Routine Versus Selective Midtrimester Ultrasound in a Poorly Resourced Setting: a Cluster Randomised Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2004
Overall Recruitment Status
Completed
Study Start Date
June 2002 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
May 2004 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
University of Johannesburg

4. Oversight

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fetal Congenital Abnormalities, Prolonged Pregnancy, Multiple Pregnancy

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
900 (false)

8. Arms, Groups, and Interventions

Intervention Type
Procedure
Intervention Name(s)
Routine midtrimester pregnany ultrasound scan
Primary Outcome Measure Information:
Title
Detection of congenital abnormalities
Title
Postterm pregnancy inductions
Secondary Outcome Measure Information:
Title
Detection of multiple pregnancies
Title
Stillbirths
Title
Neonatal morbidity
Title
Neonatal mortality

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Pregnancy, 24 weeks pregnant or less, willing to participate Exclusion Criteria: High risk pregnancy condition, e.g. poor past obstetric history, hypertensive disease, previous caesarean section
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eckhart J Buchmann, MBBCh
Organizational Affiliation
University of the Witwatersrand, Johannesburg
Official's Role
Study Chair
Facility Information:
Facility Name
University of Johannesburg
City
Johannesburg
State/Province
Gauteng
ZIP/Postal Code
2000
Country
South Africa

12. IPD Sharing Statement

Learn more about this trial

Routine Versus Selective Midtrimester Ultrasound in a Poorly Resourced Setting: a Cluster Randomised Controlled Trial

We'll reach out to this number within 24 hrs