RECRUITING

Multi-Omics for Maternal Health After Preeclampsia

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

To develop strategies to identify postpartum women at risk for adverse cardiovascular outcomes and provide them with preventative therapies.

Official Title

Multi-Omics for Maternal Health After Preeclampsia

Quick Facts

Study Start:2023-12-20
Study Completion:2028-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06340152

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 50 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Pregnant women 18 years of age to 50 years of age
  2. * 10-24 weeks gestation at time of enrollment
  3. * Singleton pregnancy
  4. * Planning to deliver at a study site (UCSD or VUMC)
  1. * Inability to give informed consent
  2. * Intrauterine fetal demise
  3. * Fetal genetic or structural anomaly
  4. * Institutionalization for psychiatric disorder, mental deficiency or incarcerated
  5. * Active or history of malignancy requiring major surgery or systemic chemotherapy
  6. * Multi-fetal gestation or a twin demise at any gestational age
  7. * Known maternal or fetal chromosomal anomalies
  8. * Patients who plan to keep their placenta after delivery

Contacts and Locations

Study Contact

Samantha La Belle
CONTACT
858-249-5985
slabelle@health.ucsd.edu
Valentina Stanley
CONTACT
momhealthstudy@health.ucsd.edu

Principal Investigator

Louise Laurent, MD, PhD
PRINCIPAL_INVESTIGATOR
UCSD
Marni Jacobs, PhD
PRINCIPAL_INVESTIGATOR
UCSD

Study Locations (Sites)

University of California, San Diego
San Diego, California, 92037
United States

Collaborators and Investigators

Sponsor: University of California, San Diego

  • Louise Laurent, MD, PhD, PRINCIPAL_INVESTIGATOR, UCSD
  • Marni Jacobs, PhD, PRINCIPAL_INVESTIGATOR, UCSD

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-12-20
Study Completion Date2028-12

Study Record Updates

Study Start Date2023-12-20
Study Completion Date2028-12

Terms related to this study

Keywords Provided by Researchers

  • hypertension
  • pregnancy
  • pre-eclampsia
  • postpartum

Additional Relevant MeSH Terms

  • Pre-Eclampsia
  • Pregnancy Induced Hypertension