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NCT01726595 · ClinicalTrials.gov registry record

Ultrasound Measurement of Reactive Hyperemia in Critical Care

A clinical trial of Critical Illness and Severe Sepsis, sponsored by University of Rochester.

Completed
Registry status
250
Enrollment target
1
Study location

NCT01726595: Completed study of Critical Illness and Severe Sepsis, sponsored by University of Rochester.

NCT01726595 is a study of Critical Illness and Severe Sepsis that has completed, run by University of Rochester. The registered enrollment target is 250 participants, below the 3,136-participant average among 91 other Critical Illness trials with a reported enrollment target (92% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01726595, a study of Critical Illness and Severe Sepsis, has completed, sponsored by University of Rochester.

COMPLETED
Registry status
250 participants
Enrollment target
1
Study location

Study Summary

The investigators hypothesize that doctors and nurses can undergo a brief period of training and then use ultrasound to accurately measure blood flow in a forearm artery after a brief period when this flow is interrupted with a blood pressure cuff, a measurement the investigators call reactive hyperemia. Reactive hyperemia indicates whether the small blood vessels in the body are healthy -- lower reactive hyperemia indicates worse small blood vessel function. When measured by experienced ultrasound experts, low reactive hyperemia strongly predicts death in critically ill patients with infection (severe sepsis). The investigators are conducting this study to determine if doctors and nurses, without specific pre-existing expertise in ultrasound, can be trained to make these measurements accurately. If so, the investigators will prove that these measurements can be applied reliably in real-world practice. The investigators also hypothesize that reactive hyperemia predict the outcomes of illness not just in patients with severe infection, but in other critically ill patients as well. Finally, the investigators hypothesize that reduced blood flow after blood pressure cuff occlusion is linked with other abnormalities of blood, previously identified in critically ill patients. For example, red blood cells from patients with severe sepsis have been shown to be stiffer than normal, so they are less able to flow along the small blood vessel passages of the body. Red blood cells become stiffer when there is a certain type of stress in the body known as "oxidative stress." If the investigators show that low reactive hyperemia, stiff red blood cells, and oxidative stress are linked, the investigators hope to develop new treatments that reduce oxidative stress, reduce the stiffness of red blood cells, and in turn improve reactive hyperemia. Improvements in reactive hyperemia indicate improvements in small blood vessel function. Better small blood vessel function means better

Study Locations (1)

New York

  • University of Rochester Medical Center - Rochester

Trial Details

FieldValue
Enrollment Target 250 participants
Start Date 2013-01
Est. Completion 2019-12
University of Rochester

636 total trials

What the finished NCT01726595 record still lists

NCT01726595 is an observational study that tracks outcomes without assigning an intervention. The registered 250 participants enrollment target is mid-sized for trials with a published cap, below the 3,136-participant average among 91 other Critical Illness trials with a reported enrollment target (92% lower).

The record links to 2 conditions, with Critical Illness appearing as the primary indexed condition, and to 0 interventions.

NCT01726595 reports a single indexed study location in New York.

Frequently Asked Questions

What is clinical trial NCT01726595 about?

NCT01726595 is a clinical study titled "Ultrasound Measurement of Reactive Hyperemia in Critical Care". The investigators hypothesize that doctors and nurses can undergo a brief period of training and then use ultrasound to accurately measure blood flow in a forearm artery after a brief period when this flow is interrupted with a blood pressure cuff, a measurement the investigators call reactive hyper...

What is the current status of trial NCT01726595?

This trial is currently completed. The enrollment target is 250 participants. The study started on 2013-01. Estimated completion is 2019-12.

What conditions does trial NCT01726595 study?

This clinical trial studies the following conditions: Critical Illness, Severe Sepsis.

Who is sponsoring clinical trial NCT01726595?

This trial is sponsored by University of Rochester, which has 636 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01726595 being conducted?

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

Similar trials for Critical Illness

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT01726595's enrollment target sits among peer trials

250 46th of 91 higher than 45 of 91 other Critical Illness trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Critical Illness 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 NCT01726595, the US trial registry maintained by the National Library of Medicine. NCT01726595 (mid enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.