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Not yet recruitingNCT07309757Updated Jan 2, 2026

Maternal Outcomes With Methamphetamine Use and Cardiac Assessment for Rural Dissemination (MOM CARD)

An observational study in Methamphetamine Abuse, sponsored by Oregon Health and Science University. Not yet recruiting. Open to female participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-01-02.

Sponsored by Oregon Health and Science University · Observational

Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
35
Ages
18 Years to 65 Years
Sex
Female
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Study summary

The purpose of this study is to develop a pilot screening protocol, comparing cardiac point-of-care ultrasound (POCUS), electrocardiogram (EKG), serum biomarkers (N-terminal pro b-type natriuretic peptide (NT-proBNP), high sensitivity troponin (hsTn)) with formal transthoracic echocardiogram (TTE) in pregnant women with methamphetamine use.

Read the detailed description

This is a pilot study that examines previously undiagnosed cardiac pathology utilizing transthoracic echocardiogram (TTE) in pregnant women with chronic methamphetamine use and assesses possible screening modalities (cardiac point-of-care ultrasound (POCUS), serum biomarkers, electrocardiogram (EKG)) in identifying underlying disease in this population. As this is a prospective observational study, we will assess pregnancy-related complications and care connections in the pilot tertiary academic setting.

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Conditions studied

  • Methamphetamine Abuse

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Keywords

  • Methamphetamine use
  • Pregnancy
  • Cardiomyopathy
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In context

Cardiomyopathies

1,176 studies on the registry are indexed under Cardiomyopathies; 287 are open to participants now.

This study's planned enrollment of 35 is below the median of 153 across 515 observational studies indexed under Cardiomyopathies.

Browse Cardiomyopathies studies →

Lead sponsor

Oregon Health and Science University is the lead sponsor of 676 studies on the registry; 136 are open to participants now.

Of its 49 completed or terminated interventional studies of FDA-regulated products, 36 (73%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
Female
Sampling method
Non-probability sample

Study population

Pregnant women > or equal to 20 weeks gestation presenting to OHSU for hospital, day patient, or observation admission will be identified via the electronic medical record.

Inclusion criteria

  • 18 years or older > 20 weeks gestation admitted to the hospital
  • Active patient-defined regular methamphetamine use for at least 1 year and any use within the last month
  • Able to understand and provide informed consent
  • Able to understand English

Exclusion criteria

Exclusion Criteria:

These criteria will exclude women whose medications, personal traits, obstetric conditions, or diseases could confound cardiovascular risk.

  • Prescribed stimulants
  • Echocardiogram or EKG previously performed during current pregnancy
  • Previous diagnosis of congestive heart dysfunction
  • Previous diagnosis of pulmonary hypertension
  • Previous myocardial infarction
  • Previous diagnosis of endocarditis
  • Prior cardiac intervention (repair of cardiac congenital lesion, valve replacement or repairs, percutaneous/operative treatment of arrhythmias)
  • High-risk aortopathy (Marfan syndrome, bicuspid aortopathy, prior aortic dissection)
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Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
35 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Sensitivity of point of care cardiac ultrasound for the detection of left ventricular systolic dysfunction as compared to comprehensive transthoracic echocardiogram.

    This outcome seeks to identify the sensitivity of point of care cardiac ultrasound for the identification of left ventricular systolic dysfunction in pregnant people who use methamphetamine when performed by an obstetrics provider, as compared to formal transthoracic echocardiogram.

    Time frame: Day 1

Secondary outcomes

  1. Sensitivity of cardiac biomarkers and ECG for the identification of left ventricular systolic dysfunction as compared to comprehensive transthoracic echocardiogram. methamphetamine

    This outcome seeks to identify the sensitivity of N-terminal pro-B-type natriuretic peptide (NT-proBNP), high sensitivity troponin and electrocardiogram for the identification of left ventricular systolic dysfunction in pregnant people who use methamphetamine, as compared to formal transthoracic echocardiogram.

    Time frame: Day 1

  2. Prevalence of underlying structural heart disease in pregnant people who use methamphetamine

    This outcome seeks to identify the prevalence of structural heart disease in pregnant people who use methamphetamine.

    Time frame: Day 1

  3. Pregnancy and delivery outcomes in people who use methamphetamine

    This outcome seeks to identify the prevalence of pregnancy delivery complications in people who use methamphetamine.

    Time frame: 3 months postpartum

  4. Changes to pregnancy-related treatment plan based on cardiovascular screening in people who use methamphetamine.

    This outcome seeks to identify linkage to cardiovascular and addiction specialty care among patients diagnosed with cardiovascular disease.

    Time frame: 3 months postpartum

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Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 2, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07309757
Lead sponsor
Oregon Health and Science University
Responsible party
Evan Shalen (Assistant Professor, Oregon Health and Science University) — Principal investigator
First posted
Dec 30, 2025
Start date
Feb 1, 2026 (estimated)
Primary completion
Dec 31, 2026 (estimated)
Completion
Dec 31, 2027 (estimated)
Last update
Jan 2, 2026

Study contacts

Evan Shalen, MD
Contact
shalen@ohsu.edu
503-494-1775
Sara McCrimmon
Contact
mccrimmo@ohsu.edu

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Dec 2025. You cannot join it, but the record below documents what was studied.

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