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NCT01248169 · ClinicalTrials.gov registry record

Impedance Cardiographic (ICG) Assessment of Pregnant Women With Severe Hypertension to Assess Impact of Standard Therapy

A clinical trial of Pregnancy; Proteinuria, With Hypertension (Severe Pre-eclampsia) and Delivery; Proteinuria, With Gestational Hypertension (Pre-eclampsia, Severe), sponsored by University of Mississippi Medical Center.

Completed
Registry status
30
Enrollment target
1
Study location

NCT01248169: Completed study of Pregnancy; Proteinuria, With Hypertension (Severe Pre-eclampsia) and Delivery; Proteinuria, With Gestational Hypertension (Pre-eclampsia, Severe), sponsored by University of Mississippi Medical Center.

NCT01248169 is a study of Pregnancy; Proteinuria, With Hypertension (Severe Pre-eclampsia) and Delivery; Proteinuria, With Gestational Hypertension (Pre-eclampsia, Severe) that has completed, run by University of Mississippi Medical Center. The registered enrollment target is 30 participants. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01248169, a study of Pregnancy; Proteinuria, With Hypertension (Severe Pre-eclampsia) and Delivery; Proteinuria, With Gestational Hypertension (Pre-eclampsia, Severe), has completed, sponsored by University of Mississippi Medical Center.

COMPLETED
Registry status
30 participants
Enrollment target
1
Study location

Study Summary

The utilization of external cardiohemodynamic patient assessment, applying non-invasive stick-on contact patches to the mother's neck on either side and chest wall on either side, enables the practitioner to have information about the patient's cardiac function and vascular status beyond simply blood pressure and pulse. This information, once collected, should open the practitioner's eyes to better assess the patient's disease status and her response to therapy. We will use this information to compare the effectiveness of the two standard medications used for treatment of maternal high blood pressure.

Primary Outcome

ICG test is performed on pregnant women before receiving any antihypertensive medication. Labetalol and Hydralazine, two ot the most commonly used antihypertensives to treat high blood pressure in pregnant women will be used in this study.

Study Locations (1)

Mississippi

  • Wiser Hospital for Women and Infants at the University of Mississippi Medical Center - Jackson

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2009-12
Est. Completion 2013-11

What the finished NCT01248169 record still lists

NCT01248169 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 30 participants, a relatively small participant target.

The record links to 3 conditions, with Pregnancy; Proteinuria, With Hypertension (Severe Pre-eclampsia) appearing as the primary indexed condition, and to 0 interventions.

NCT01248169 reports a single indexed study location in Mississippi.

Frequently Asked Questions

What is clinical trial NCT01248169 about?

NCT01248169 is a clinical study titled "Impedance Cardiographic (ICG) Assessment of Pregnant Women With Severe Hypertension to Assess Impact of Standard Therapy". The utilization of external cardiohemodynamic patient assessment, applying non-invasive stick-on contact patches to the mother's neck on either side and chest wall on either side, enables the practitioner to have information about the patient's cardiac function and vascular status beyond simply bloo...

What is the current status of trial NCT01248169?

This trial is currently completed. The enrollment target is 30 participants. The study started on 2009-12. Estimated completion is 2013-11.

What conditions does trial NCT01248169 study?

This clinical trial studies the following conditions: Pregnancy; Proteinuria, With Hypertension (Severe Pre-eclampsia), Delivery; Proteinuria, With Gestational Hypertension (Pre-eclampsia, Severe), Pregnancy; Hypertension, Gestational Hypertension, With Albuminuria (Severe Pre-eclampsia).

Who is sponsoring clinical trial NCT01248169?

This trial is sponsored by University of Mississippi Medical Center, which has 96 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01248169 being conducted?

This trial has 1 study location across Mississippi. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT01248169, the US trial registry maintained by the National Library of Medicine. NCT01248169 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.