Fort Sam Houston, TXNCT06699901Now EnrollingIRB Ready

Adverse Effects in the Therapeutic Use of Other and Unspecified Agents Affecting Blood Constituents Clinical Trial in Fort Sam Houston, TX

Access cutting-edge adverse effects in the therapeutic use of other and unspecified agents affecting blood constituents treatment through this clinical trial at a research site in Fort Sam Houston. Study-provided care at no cost to qualified participants.

Sponsored by Brooke Army Medical Center

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Why Participate?

  • No-Cost Study Care

  • Local to Fort Sam Houston

    Convenient for TX residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Fort Sam Houston site if eligible
  4. 4Begin participation

About This Adverse Effects in the Therapeutic Use of Other and Unspecified Agents Affecting Blood Constituents Study in Fort Sam Houston

Combat and civilian trauma frequently result in open wounds that are at risk for infection. Data from the Department of Defense Trauma Registry demonstrate that 74% of combat trauma casualties have an open wound. The Committee on Tactical Combat Casualty Care, the Prolonged Field Care Working Group, and the Joint Trauma System clinical practice guidelines recommend antibiotic prophylaxis for open wounds after trauma. The civilian setting has similar risks of open wound infection after trauma. In parallel, current practice guidelines recommend the aggressive use of balanced blood products during resuscitation. It remains unclear how the replacement of blood after hemorrhage through transfusion may affect antibiotic concentrations. Data is necessary to better understand this relationship to enhance wound prophylaxis antibiotic dosing, particularly in severely wounded casualties who receive blood products during massive transfusions. It remains unclear how these resuscitation methods may alter pharmacokinetics. The investigators hypothesize that drug concentrations decrease in direct relation to the amount of blood transfused during low-volume, massive, and supermassive transfusion after trauma compared to patients who receive no blood products. The investigators seek to understand the relationship between drug concentrations and blood product administration using a non-compartmentalized model in the setting of hemorrhage. Specifically, they will (1) obtain drug concentrations at regular intervals during the first 12-18 hours after administration of antibiotics, (2) determine how much blood products and fluids are transfused during the 12 hours prior to antibiotic and 24 hours post-administration, and (3) perform data modeling to understand the relationship between blood transfusions and drug concentrations to inform data-driven dosing models. Liquid chromatography methods will be developed to measure drug concentrations. The investigators will conduct a prospective, multicenter study at two large trauma centers - Brooke Army Medical Center and the University of Colorado Hospital. They will seek to enroll any participant who is hospitalized or anticipated hospital admission for acute trauma and receives an antibiotic on the study list during their index hospitalization. They will then model the drug levels against the amount of blood and fluid infused to create an understanding of the pharmacokinetics of antibiotic wound prophylaxis.

Sponsor: Brooke Army Medical Center

Who Can Participate

Inclusion Criteria

Receives ampicillin/sulbactam, cefazolin, cefepime, ceftriaxone, clindamycin, ertapenem, levofloxacin, metronidazole or pipercillin/tazobactam at any dose
Hospitalized or anticipated hospital admission

Exclusion Criteria

Received the same antibiotic within the past 5 half-lives of the drug (e.g. received the same antibiotic during a recent interval)
\<18 years of age
Known pregnancy
Known Prisoner

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Fort Sam Houston?

Yes, this clinical trial (NCT06699901) has an active research site in Fort Sam Houston, TX that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Adverse Effects in the Therapeutic Use of Other and Unspecified Agents Affecting Blood Constituents Treatment Options in Fort Sam Houston, TX

If you're searching for adverse effects in the therapeutic use of other and unspecified agents affecting blood constituents treatment options in Fort Sam Houston, TX, this clinical trial (NCT06699901) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Fort Sam Houston research site is actively enrolling participants for this clinical trial. You'll receive care from experienced adverse effects in the therapeutic use of other and unspecified agents affecting blood constituents specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

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