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Medication Use Evaluation (MUE) for Continuous Heparin Infusions in Hospitalized Patients

Medication Use Evaluation (MUE) for Continuous Heparin Infusions in Hospitalized Patients

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06096064
Enrollment
100
Registered
2023-10-23
Start date
2022-10-31
Completion date
2023-08-21
Last updated
2026-03-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Unfractionated Heparin

Brief summary

Unfractionated heparin (UFH) is an anticoagulant to prevent thrombus formation or worsening of an existing thrombus. It is indicated for patients with deep vein thrombosis/pulmonary embolism (DVT/PE) or acute coronary syndrome (ACS). Unfractionated heparin treatment consists of an initial bolus followed by a continuous infusion that is adjusted based on the patient's subsequent partial thromboplastin time (PTT) levels

Detailed description

Unfractionated heparin is classified as a high-alert medication in the acute care setting.3 Therapeutic anticoagulation is a high priority for healthcare teams because the impacts of inadequate anticoagulation can lead to life threatening events such as a major bleed or thrombus formation and/or death.

Interventions

None listed

Sponsors

Methodist Health System
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Patient's aged 18 years or older with a confirmed diagnosis of DVT/PE based on imaging or a confirmed diagnosis of ACS requiring heparin therapy

Exclusion criteria

* History of bleeding in the last 30 days * History of HIT * Use of systemic anticoagulants for another indication * Presence of coagulation disorder prior to admission (i.e. hemophilia, sickle cell anemia, etc.)

Design outcomes

Primary

MeasureTime frameDescription
Incidents of deviations from protocol30 DaysAppropriate anticoagulation management will be measured using Percent time in therapeutic range based on aPTT levels

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 25, 2026