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Recruiting NCT07420465

NCT07420465 Cardiometabolic Risk in Pregnancy and Postpartum

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Clinical Trial Summary
NCT ID NCT07420465
Status Recruiting
Phase
Sponsor Forgive Avorgbedor
Condition Hypertensive Disorders of Pregnancy
Study Type INTERVENTIONAL
Enrollment 200 participants
Start Date 2026-04-01
Primary Completion 2027-06-28

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age 45 Years
Study Type INTERVENTIONAL
Interventions
Postpartum Cardiovascular Disease (CVD) Risk Reduction ProgramEnhanced Postpartum Care

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 200 participants in total. It began in 2026-04-01 with a primary completion date of 2027-06-28.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The goal of this study is to evaluate changes in blood pressure and early cardiovascular risk markers and to determine whether a postpartum education intervention can improve cardiovascular risk monitoring among pregnant women in their third trimester through six months postpartum in Accra, Ghana. The study includes women aged 18 years and older with and without pregnancy-related cardiometabolic complications. Findings from this study will inform the development of scalable postpartum screening and intervention strategies to reduce long-term cardiovascular disease risk among women.

Eligibility Criteria

Inclusion Criteria: * Singleton pregnancy * 18 years and older * 3rd trimester of pregnancy at enrollment * Will be living in the area for the study duration * Women with or without pregnancy complications (e.g., gestational hypertension, preeclampsia, gestational diabetes) Exclusion Criteria: * Multiple births * Diagnosed CVD or diabetes prior to pregnancy * Renal or other serious maternal diseases pre-pregnancy

Contact & Investigator

Central Contact

Forgive Avorgbedor, PhD

✉ f-avorgbedo@uncg.edu

📞 336-334-5111

Principal Investigator

Samuel Dery, PhD

STUDY DIRECTOR

University of Ghana

Frequently Asked Questions

Who can join the NCT07420465 clinical trial?

This trial is open to female participants only, aged 18 Years or older, up to 45 Years, studying Hypertensive Disorders of Pregnancy. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07420465 currently recruiting?

Yes, NCT07420465 is actively recruiting participants. Contact the research team at f-avorgbedo@uncg.edu for enrollment information.

Where is the NCT07420465 trial being conducted?

This trial is being conducted at Accra, Ghana.

Who is sponsoring the NCT07420465 clinical trial?

NCT07420465 is sponsored by Forgive Avorgbedor. The principal investigator is Samuel Dery, PhD at University of Ghana. The trial plans to enroll 200 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology