Sickle Cell Disease Obstetric Multi-Disciplinary Care Programme
NCT ID: NCT05143021
Last Updated: 2026-01-30
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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ACTIVE_NOT_RECRUITING
500 participants
OBSERVATIONAL
2022-02-14
2027-02-28
Brief Summary
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Detailed Description
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The critical and unanswered question is: can the dramatic reduction in maternal and perinatal mortalities observed at KBTH be maintained and replicated with high fidelity at other tertiary hospitals in Ghana? This study, set in a region with the world's highest SCD prevalence, has the potential to impact maternal and neonatal mortality by tailoring evidence-based protocols to facilitate use by non-specialized health care providers. This project has the potential to change the way pregnant women with SCD are managed in Ghana and the rest of sub-Saharan Africa. If successful, this study will form a blueprint for the scale-up of this evidence-based protocol across the country and the West Africa sub-region, where pregnant women with SCD face an uncertain future. Additionally, the project can serve as a model for training clinical researchers, public health, and social scientists in implementation science for major interventions in maternal and perinatal health in Ghana.
The investigators propose a standards care prospective protocol to test the following two primary hypotheses:
1. After implementing a hospital-tailored task-shifting intervention program in the tertiary hospitals, there will be a 60% relative risk reduction in maternal mortality among pregnant women with SCD.
2. A. There will be at least a 90% fidelity to evidence-based guidelines for the prevention of ACS for women with SCD at high risk for ACS (acute pain and post-surgery) B. There will be at least a 90% fidelity to evidence-based guidelines for the treatment of ACS for women with SCD at high risk for ACS (acute pain and post-surgery)
This will be a multi-center prospective cohort study involving pregnant women with SCD who attend antenatal care at three referral hospitals. Participants will be enrolled from the booking visit over 18 months and managed with the evidence-based clinical guidelines plus multi-disciplinary team standard care protocol and followed up prospectively until delivery and up to six weeks after delivery.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Pregnant Women with Sickle Cell Disease
Pregnant women with sickle cell disease from the 3 centers in Ghana
Multidisciplinary Sickle Cell Disease- Obstetric Team
Modified multidisciplinary teams for pregnant women with sickle cell disease including members from an obstetrics team and sickle cell disease team.
Interventions
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Multidisciplinary Sickle Cell Disease- Obstetric Team
Modified multidisciplinary teams for pregnant women with sickle cell disease including members from an obstetrics team and sickle cell disease team.
Eligibility Criteria
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Inclusion Criteria
* Confirmed SCD status by Hb-electrophoresis in alkaline medium
* Pregnancy should be confirmed by urine or blood pregnancy test and pelvic ultrasound scan.
Exclusion Criteria
* All pregnant women with SCD who present to the Greater Accra Regional Hospital or Tamale Teaching Hospital for acute admissions, labor, and delivery
* All pregnant women with SCD with undetermined Hb phenotypes on Hb electrophoresis.
18 Years
45 Years
FEMALE
No
Sponsors
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Vanderbilt University Medical Center
OTHER
Responsible Party
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Michael DeBaun
Director of Vanderbilt-Meharry Center of Excellence for Sickle Cell Disease
Principal Investigators
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Leshana St. Jean, PhD
Role: STUDY_DIRECTOR
Vanderbilt University Medical Center
Locations
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Greater Accra Regional Hospital
Accra, , Ghana
Korle Bu Teaching Hospital
Accra, , Ghana
Tamale Teaching Hospital
Tamale, , Ghana
Countries
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Other Identifiers
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211778
Identifier Type: -
Identifier Source: org_study_id
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