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NCT03129542 · ClinicalTrials.gov registry record · Phase 1

Midodrine Hydrochloride in Early Sepsis

A Phase 1 study, sponsored by Mayo Clinic.

Completed
Registry status
Phase 1
Development phase
33
Enrollment target

NCT03129542: Completed Phase 1 study, sponsored by Mayo Clinic.

NCT03129542 is a Phase 1 study that has completed, run by Mayo Clinic. The registered enrollment target is 33 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (45% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT03129542, a Phase 1 study, has completed, sponsored by Mayo Clinic.

COMPLETED
Registry status
Phase 1
Development phase
33 participants
Enrollment target

Study Summary

The investigators would like to determine if early administration of oral Midodrine in participants diagnosed with sepsis will impact blood pressures and decrease the need for and/or doses of intravenous pressor agents.

Primary Outcome

To study the duration of vasopressor use in the first 24 hours of sepsis

Interventions

  • DRUG Placebo capsule
  • DRUG Midodrine Hydrochloride 10 milligrams

Trial Details

FieldValue
Enrollment Target 33 participants
Start Date 2017-08-30
Est. Completion 2020-05-15
Phase Phase 1
Mayo Clinic

2,844 total trials

What the finished NCT03129542 record still lists

NCT03129542 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 33 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (45% lower).

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

NCT03129542 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03129542 about?

NCT03129542 is a clinical study titled "Midodrine Hydrochloride in Early Sepsis". The investigators would like to determine if early administration of oral Midodrine in participants diagnosed with sepsis will impact blood pressures and decrease the need for and/or doses of intravenous pressor agents.

What is the current status of trial NCT03129542?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 33 participants. The study started on 2017-08-30. Estimated completion is 2020-05-15.

What interventions are being tested in trial NCT03129542?

The interventions under investigation include: Placebo capsule (DRUG), Midodrine Hydrochloride 10 milligrams (DRUG).

Who is sponsoring clinical trial NCT03129542?

This trial is sponsored by Mayo Clinic, which has 2,844 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03129542's enrollment target sits among peer trials

33 1280th of 2000 higher than 705 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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 NCT03129542, the US trial registry maintained by the National Library of Medicine. NCT03129542 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.