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NCT00937001 · ClinicalTrials.gov registry record · NA

Critical Illness Myopathy as a Cause of Debilitating ICU-Acquired Weakness

A NA study of Cognitive Impairment and Myopathy, sponsored by Vanderbilt University.

Active
Registry status
NA
Development phase
50
Enrollment target
1
Study location

NCT00937001: Active NA study of Cognitive Impairment and Myopathy, sponsored by Vanderbilt University.

NCT00937001 is a NA study of Cognitive Impairment and Myopathy that is active but no longer recruiting, run by Vanderbilt University. The registered enrollment target is 50 participants, below the 665-participant average among 105 other Cognitive Impairment 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

NCT00937001, a NA study of Cognitive Impairment and Myopathy, is active but no longer recruiting, sponsored by Vanderbilt University.

ACTIVE NOT RECRUITING
Registry status
NA
Development phase
50 participants
Enrollment target
1
Study location

Study Summary

ICU-acquired weakness represents a common and often devastating disease process which affects greater than 50% of critically ill patients. This pathogenesis of this acquired disease is multifactorial and results in variable severity, ranging from mild, transient to severe, permanent dysfunction of peripheral nerves in additional to muscle. In affected patients, weakness may persist for months to years after the acute phase of their illness, and has been implicated as a major contributor to decreased functional status and quality of life. Muscle ultrasound has been validated for assessment of muscle size as well as diagnosis of myopathic and neuropathic changes in patients with other known neuromuscular diseases. The use of muscle ultrasound or other imaging modalities for diagnosis or monitoring of ICU-acquired weakness has not been studied, although a single study using muscle ultrasound has shown significant change in muscle size in ICU patients receiving high dose corticosteroids and a prolonged course of paralytic agents. The investigators plan to use multiple modalities to examine skeletal muscle catabolism, function, and structure in patients during critical illness and recovery. The investigators will combine physical exam, hand grip dynamometry, electrophysiologic studies, serum biomarkers, muscle biopsies, and muscle ultrasound to assess a group of critically ill patients during their hospital stay. The investigators will obtain additional data, including neuropsychiatric assessments, severity of illness scores, administration of potentially harmful medications, and pertinent daily laboratory data. This study will last approximately 12 months.

Interventions

  • PROCEDURE Biopsy/Ultrasound

Study Locations (1)

Tennessee

  • Vanderbilt University - Nashville

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2008-11
Est. Completion 2026-12
Phase NA
Vanderbilt University

430 total trials

What the registry record for NCT00937001 still lists

NCT00937001 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 665-participant average among 105 other Cognitive Impairment trials with a reported enrollment target (92% lower).

The record links to 2 conditions, with Cognitive Impairment appearing as the primary indexed condition, and to 1 intervention - of which Biopsy/Ultrasound is the first listed.

NCT00937001 reports a single indexed study location in Tennessee.

Frequently Asked Questions

What is clinical trial NCT00937001 about?

NCT00937001 is a clinical study titled "Critical Illness Myopathy as a Cause of Debilitating ICU-Acquired Weakness". ICU-acquired weakness represents a common and often devastating disease process which affects greater than 50% of critically ill patients. This pathogenesis of this acquired disease is multifactorial and results in variable severity, ranging from mild, transient to severe, permanent dysfunction of p...

What is the current status of trial NCT00937001?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 50 participants. The study started on 2008-11. Estimated completion is 2026-12.

What conditions does trial NCT00937001 study?

This clinical trial studies the following conditions: Cognitive Impairment, Myopathy.

What interventions are being tested in trial NCT00937001?

The interventions under investigation include: Biopsy/Ultrasound (PROCEDURE).

Who is sponsoring clinical trial NCT00937001?

This trial is sponsored by Vanderbilt University, which has 430 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00937001 being conducted?

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

Similar trials for Cognitive Impairment

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 NCT00937001's enrollment target sits among peer trials

50 71st of 105 higher than 33 of 105 other Cognitive Impairment trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Cognitive Impairment 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 NCT00937001, the US trial registry maintained by the National Library of Medicine. NCT00937001 (small enrollment · single site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.