Dallas, TXNCT05910567Now EnrollingIRB Ready

Blunt Trauma to Abdomen Clinical Trial in Dallas, TX

Access cutting-edge blunt trauma to abdomen treatment through this clinical trial at a research site in Dallas. Study-provided care at no cost to qualified participants.

Sponsored by University of California, Davis

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Expert Care in Dallas

Access blunt trauma to abdomen specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related blunt trauma to abdomen treatment provided free

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Check if you qualify for this blunt trauma to abdomen clinical trial in Dallas, TX

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Why Participate?

  • No-Cost Study Care

  • Local to Dallas

    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 Dallas site if eligible
  4. 4Begin participation

About This Blunt Trauma to Abdomen Study in Dallas

Bleeding from intra-abdominal injuries is a leading cause of traumatic deaths in children. Abdominal CT is the reference standard test for diagnosing intra-abdominal injuries. Compelling reasons exist, however, to both aggressively evaluate injured children for intra-abdominal injuries with CT and to limit abdominal CT evaluation to solely those at non-negligible risk. The focused assessment sonography for trauma (FAST) examination can help focus patient evaluation in just this manner by potentially safely decreasing abdominal CT use in low risk children. This research study is a multicenter, randomized, controlled trial to determine whether use of the FAST examination, a bedside abdominal ultrasound, impacts care in 3,194 hemodynamically stable children with blunt abdominal trauma. The overall objectives of this proposal are 1) to determine the efficacy of using the FAST examination during the initial evaluation of children with blunt abdominal trauma, and 2) to identify factors associated with abdominal CT use in children considered very low risk for IAI after a negative FAST examination. The long-term objective of the research is to determine appropriate evaluation strategies to optimize the care of injured children, leading to improved quality of care and a reduction in morbidity and mortality.

Sponsor: University of California, Davis

Who Can Participate

Inclusion Criteria

. Inclusion Criteria:
Blunt torso trauma resulting from a significant mechanism of injury:
Motor vehicle collision: greater than 60 mph, ejection, or rollover
Automobile versus pedestrian/bicycle: automobile speed \> 25 mph
Falls greater than 20 feet in height
Crush injury to the torso
Physical assault involving the abdomen
Decreased level of consciousness (Glasgow Coma Scale (GCS) score 9-14 or below age-appropriate behavior) in association with blunt torso trauma
Blunt traumatic event with any of the following (regardless of the mechanism):
Extremity paralysis
Multiple long bone fractures (e.g., tibia and humerus fracture)
History and physical examination suggestive of blunt torso trauma of any mechanism (including mechanisms of injury of less severity than mentioned above)

Exclusion Criteria

and meet any one of the following inclusion criteria. Inclusion Criteria:
Blunt torso trauma resulting from a significant mechanism of injury:
Motor vehicle collision: greater than 60 mph, ejection, or rollover
Automobile versus pedestrian/bicycle: automobile speed \> 25 mph
Falls greater than 20 feet in height
Crush injury to the torso
Physical assault involving the abdomen
Decreased level of consciousness (Glasgow Coma Scale (GCS) score 9-14 or below age-appropriate behavior) in association with blunt torso trauma
Blunt traumatic event with any of the following (regardless of the mechanism):
Extremity paralysis
Multiple long bone fractures (e.g., tibia and humerus fracture)
History and physical examination suggestive of blunt torso trauma of any mechanism (including mechanisms of injury of less severity than mentioned above) Exclusion Criteria: The following patients will be excluded from the study:
Age-adjusted low blood pressure (Hemodynamic instability)
Patients will be excluded for prehospital or initial age-adjusted ED low blood pressure. This is because the standard evaluation of these patients involves immediate FAST based on prior work by our group. Low blood pressure is determined based upon the patient's age, and will be defined as a systolic blood pressure less than 70 mm Hg for patients younger than 1 month, less than 80 mm Hg for ages 1 month to 5 years, and less than 90 mm Hg for ages over 5 years.
Penetrating trauma: Patients who are victims of stab or gunshot wounds
Traumatic injury occurring \> 24 hours prior to the time of presentation to the ED
Transfer of the patient to the ED from an outside facility with abdominal CT scan, diagnostic peritoneal lavage, or laparotomy previously performed
Transferred with FAST exam already performed at outside hospital
Patients with known disease processes resulting in intraperitoneal fluid including liver failure and the presence of ventriculoperitoneal shunts
Initial GCS score ≤ 8 as it is standard for children with GCS scores ≤ 8 to undergo abdominal CT if blunt abdominal trauma is suspected
Known pregnancy
Known prisoner
Known intra-abdominal injury diagnosed within 30 days prior of this ED visit

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 Dallas?

Yes, this clinical trial (NCT05910567) has an active research site in Dallas, 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.

Blunt Trauma to Abdomen Treatment Options in Dallas, TX

If you're searching for blunt trauma to abdomen treatment options in Dallas, TX, this clinical trial (NCT05910567) 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 Dallas research site is actively enrolling participants for this clinical trial. You'll receive care from experienced blunt trauma to abdomen 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.

Looking for more options? Browse all blunt trauma to abdomen clinical trials near you to find additional studies recruiting in your area.

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