Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00585182 · ClinicalTrials.gov registry record · Phase 4

Study to Evaluate Weight-based Enoxaparin Dosing in Obese Medical Patients at Risk for DVT

A Phase 4 study, sponsored by University of Utah.

Completed
Registry status
Phase 4
Development phase
28
Enrollment target

NCT00585182: Completed Phase 4 study, sponsored by University of Utah.

NCT00585182 is a Phase 4 study that has completed, run by University of Utah. The registered enrollment target is 28 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00585182, a Phase 4 study, has completed, sponsored by University of Utah.

COMPLETED
Registry status
Phase 4
Development phase
28 participants
Enrollment target

Study Summary

Deep vein thrombosis(DVT) is a common complication in hospitalized medical patients. Consensus guidelines recommend using medications such as heparin or low-molecular-weight heparins (LMWH) to prevent DVT in these patients. Generally, these medications are given in a fixed dose that is the same for everyone. The appropriate dose of medication in patients with severe obesity is uncertain. There is some evidence that the use of standard fixed-doses in severely obese patients may not provide adequate protection against DVT. The purpose of this study is to evaluate a weight-based dose(0.5 milligrams per kilogram of body weight) of the commonly prescribed LMWH, enoxaparin in severely obese patients to determine if predictable levels of blood thinning can be achieved. We hypothesize that dosing enoxaparin 0.5mg/kg once daily in severely obese patients will lead to predictable blood levels.

Primary Outcome

The Rotachrom® assay using the STA-Compact instrument (Diagnostica Stago, Parsippany, NJ) was used to quantitate anti- Xa (LMWH) activity for enoxaparin. The sensitivity of this assay is 0.2 U/mL and within run imprecision is 5.5 (% CV) at 1 U/mL. The assay is linear between 0.2-2.0 U/mL

Interventions

  • DRUG Enoxaparin 0.5 mg/kg once daily

Trial Details

FieldValue
Enrollment Target 28 participants
Start Date 2007-01
Est. Completion 2008-04
Phase Phase 4
University of Utah

818 total trials

What the finished NCT00585182 record still lists

NCT00585182 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 28 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (95% lower).

The record links to 0 conditions, and to 1 intervention - of which Enoxaparin 0.5 mg/kg once daily is the first listed.

NCT00585182 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00585182 about?

NCT00585182 is a clinical study titled "Study to Evaluate Weight-based Enoxaparin Dosing in Obese Medical Patients at Risk for DVT". Deep vein thrombosis(DVT) is a common complication in hospitalized medical patients. Consensus guidelines recommend using medications such as heparin or low-molecular-weight heparins (LMWH) to prevent DVT in these patients. Generally, these medications are given in a fixed dose that is the same for ...

What is the current status of trial NCT00585182?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 28 participants. The study started on 2007-01. Estimated completion is 2008-04.

What interventions are being tested in trial NCT00585182?

The interventions under investigation include: Enoxaparin 0.5 mg/kg once daily (DRUG).

Who is sponsoring clinical trial NCT00585182?

This trial is sponsored by University of Utah, which has 818 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00585182's enrollment target sits among peer trials

28 1635th of 2000 higher than 350 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03471117 · 28 participants · Phase 4

    Pioglitazone to Reduce Sympathetic Overactivity in CKD Patients

  • NCT03523975 · 28 participants · Phase 1

    Venetoclax, Lenalidomide and Rituximab in Patients With Previously Untreated Mantle Cell Lymphoma

  • NCT03608631 · 28 participants · Phase 1

    iExosomes in Treating Participants With Metastatic Pancreas Cancer With KrasG12D Mutation

  • NCT03810651 · 28 participants · Early Phase 1

    Pencil Beam Scanning in Patients With Renal Tumors

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00585182, the US trial registry maintained by the National Library of Medicine. NCT00585182 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.