TerminatedNot Applicable

Non-invasive Versus Invasive Blood Pressure Measurement in the Morbidly Obese Parturient With Severe Preeclampsia

Stopped: Changes in standard of care have altered the feasibility of the study.

United States3 participantsStarted 2015-05-01

Plain-language summary

The study will compare agreement of invasive blood pressure measurements with non-invasive blood pressure measurements measured with a conical blood pressure and large standard upper arm rectangular cuff in morbidly obese severely hypertensive (systolic blood pressure \> 160 mmHg) parturients.

Who can participate

Age range18 Years

SexFEMALE

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Written, signed and dated informed consent * ≥ 18 years of age * BMI \>40 kg/m2 * Has a clinically indicated radial artery line already in situ or who agree to placement of an arterial line * Systolic blood pressure \>160 mm Hg * Gestational age greater than or equal to 24 weeks * Parturients admitted for induction of labor Exclusion Criteria: * Parturients admitted in labor

What they're measuring

Comparison of Noninvasive Systolic Blood Pressure Readings to Invasive Blood Pressure Measurement

Timeframe: Single time point measurement (1 day)

Trial details

NCT IDNCT03222414

SponsorVanderbilt University Medical Center

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2016-01-18

Results submitted2019-11-20

View on ClinicalTrials.gov More Pre-Eclampsia trials