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 ChemoprophylaxisHospitalized 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
- Evaline W Kihara, MSN, APRN, AGACNP-BC, CCRN(713) 500-6362
- Nikhil Padhye, PhD(713) 500-2035
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| HCA Houston Northwest Medical Center | Houston | Texas | 77090 |
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