Circadian Variation of Anti-Factor Xa in Hospitalized Trauma Patients

Part of paid clinical trials in Houston, Texas.

Sponsor
The University of Texas Health Science Center, Houston
Study ID
NCT07856641
Status
Recruiting

Conditions

  • Circadian Variation in Anti-Factor Xa (Anti-FXa) Activity

Eligibility Criteria

Sex
ALL
Age
18 Years - 80 Years
Healthy Volunteers
Not accepted

Study Details

The purpose of this study is to determine whether a circadian rhythm exists in anti-FXa levels and AT3 activity in hospitalized trauma patients receiving low-molecular-weight heparin (LMWH) chemoprophylaxis

Key Dates

First listed
Oct 2, 2026
Start date
Aug 26, 2026
Status verified
Sep 2026
Primary completion
Aug 26, 2027
Completion
Mar 26, 2028

Study Design

Enrollment
40 participants (estimated)

Arms

  • Arm: Hospitalized Trauma Patients Receiving LMWH Chemoprophylaxis
    Hospitalized trauma patients receiving low-molecular-weight heparin (LMWH) chemoprophylaxis as part of routine clinical care. Participants will have anti-FXa levels and antithrombin III (AT3) activity measured at predefined time points to evaluate potential circadian variation in these measures.

Primary Outcome Measure

Change in anti-factor Xa (anti-FXa) levels [ Time Frame: 4 hours after the 3rd LMWH dose (T0), then every 6 hours (T6, T12, T18) ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
HCA Houston Northwest Medical CenterHoustonTexas77090
Evaline W Kihara, MSN, APRN, AGACNP-BC, CCRN
(713) 500-6362
Nikhil Padhye
(713) 500-2035

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