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NCT05928624 · ClinicalTrials.gov registry record · NA

A Pilot Trial to Test the Feasibility of Utilizing Home Blood Pressure Monitoring to Optimize the Administration of Midodrine Among Decompensated Cirrhosis Patients

A NA study, sponsored by University of California, San Francisco.

Completed
Registry status
NA
Development phase
69
Enrollment target

NCT05928624: Completed NA study, sponsored by University of California, San Francisco.

NCT05928624 is a NA study that has completed, run by University of California, San Francisco. The registered enrollment target is 69 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05928624, a NA study, has completed, sponsored by University of California, San Francisco.

COMPLETED
Registry status
NA
Development phase
69 participants
Enrollment target

Study Summary

This is a randomized single-blind feasibility trial to test the utilization of home blood pressure devices to improve the clinical management of decompensated cirrhosis patients.

Primary Outcome

The investigators will compare the change in mean arterial pressure before and after utilization of the data generated from the home monitoring.

Interventions

  • OTHER Standard of Care
  • DEVICE Withings Home Blood Pressure Device and Scale

Trial Details

FieldValue
Enrollment Target 69 participants
Start Date 2023-09-22
Est. Completion 2024-07-01
Phase NA

What the finished NCT05928624 record still lists

NCT05928624 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 69 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).

The record links to 0 conditions, and to 2 interventions - of which Standard of Care is the first listed.

NCT05928624 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05928624 about?

NCT05928624 is a clinical study titled "A Pilot Trial to Test the Feasibility of Utilizing Home Blood Pressure Monitoring to Optimize the Administration of Midodrine Among Decompensated Cirrhosis Patients". This is a randomized single-blind feasibility trial to test the utilization of home blood pressure devices to improve the clinical management of decompensated cirrhosis patients.

What is the current status of trial NCT05928624?

This trial is currently completed. It is a NA study. The enrollment target is 69 participants. The study started on 2023-09-22. Estimated completion is 2024-07-01.

What interventions are being tested in trial NCT05928624?

The interventions under investigation include: Standard of Care (OTHER), Withings Home Blood Pressure Device and Scale (DEVICE).

Who is sponsoring clinical trial NCT05928624?

This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05928624's enrollment target sits among peer trials

69 1133rd of 2000 higher than 868 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05928624, the US trial registry maintained by the National Library of Medicine. NCT05928624 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.