Salt Lake City, UTNCT07563296Now EnrollingIRB Ready

PTSD and Trauma-related Symptoms Clinical Trial in Salt Lake City, UT

Access cutting-edge ptsd and trauma-related symptoms treatment through this phase 2 clinical trial at a research site in Salt Lake City. Study-provided care at no cost to qualified participants.

Sponsored by Irma Fleming

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Expert Care in Salt Lake City

Access ptsd and trauma-related symptoms specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related ptsd and trauma-related symptoms treatment provided free

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Check if you qualify for this ptsd and trauma-related symptoms clinical trial in Salt Lake City, UT

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Salt Lake City

    Convenient for UT 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 Salt Lake City site if eligible
  4. 4Begin participation

About This PTSD and Trauma-related Symptoms Study in Salt Lake City

A study looking at the safety and tolerability of KAP (Ketamine-Assisted Psychotherapy) in the burn population.

Sponsor: Irma Fleming

Who Can Participate

Inclusion Criteria

Subjects 18 - 65 yrs with \> 15 % Total Body Surface Area Burns.
National Stressful Events Survey Acute Stress Disorder Short Scale (NSESSS) average total score\>= 2 (severity scale of none (0), mild (1), moderate (2), severe (3), or extreme (4) ) prior to discharge from UUH.

Exclusion Criteria

Allergy or previous adverse reactions to ketamine
Pending surgical interventions
Active systemic infection, sepsis, or hemodynamic instability
Physical limitations from burn injury that preclude safe travel to outpatient visits or positioning for therapy.
Lack of reliable transportation, caregiver support, or housing stability.
Language barrier
Personal history or first- or second-degree relatives with schizophrenia, bipolar affective disorder, delusional disorder, schizoaffective disorder, psychosis, or other psychotic spectrum illness.
Currently meeting DSM-5 criteria for Dissociative Disorder, or other psychiatric conditions judged to be incompatible with the establishment of rapport or safe exposure to ketamine.
Currently meeting DSM-5 criteria for Cluster B Personality Disorder.
Severe depression requiring immediate standard-of-care treatment (e.g., hospitalization).
Suicidal ideation over the past month as assessed as a yes to question 3, 4, or 5 on the Columbia-Suicide Severity Rating Scale, Suicidal Ideation section
Current or prior history of PTSD diagnosis
Current or history within the last two years of meeting DSM-V criteria of substance use disorder (excluding caffeine and nicotine).
Current substance use disorders may be identified through the drug urine screening test or undergoing treatment (methadone/Suboxone) .
Congestive heart failure, including all New York Heart Association Classes.
Angina pectoris, cardiac hypertrophy, cardiac ischemia, myocardial infarction
Uncontrolled hypertension at the time of enrollment (BP\>140 systolic or 90 diastolic), coronary artery disease, artificial heart valve
Prolonged or congenital long QT syndrome (\>450 ms), serious cardiac arrhythmias, tachycardia, a clinically significant screening ECG abnormality
History of hypersensitivity to ketamine
Receiving ketamine treatments for psychiatric condition within the past 6 months
Seizure disorder
Moderate to severe dementia
History of significant traumatic brain injury
Requires the use of supplemental oxygen.
Require Propranolol for Burn Hypermetabolism
Any other condition that would, in the Investigator's judgment, contraindicate the subject's participation in the clinical study due to safety concerns or compliance with clinical study procedures (e.g., infection/inflammation, intestinal obstruction, unable to swallow medication, \[patients may not receive the drug through a feeding tube\], social/ psychological issues, etc.)
Subjects taking prohibited medications. A washout period of prohibited medications for a period of at least five half-lives should occur prior to study registration. These medications include antipsychotic medications, doses of benzodiazepines in excess of 20mg diazepam equivalents per day.

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 Salt Lake City?

Yes, this clinical trial (NCT07563296) has an active research site in Salt Lake City, UT 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.

PTSD and Trauma-related Symptoms Treatment Options in Salt Lake City, UT

If you're searching for ptsd and trauma-related symptoms treatment options in Salt Lake City, UT, this clinical trial (NCT07563296) 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 Salt Lake City research site is actively enrolling participants for this phase 2 clinical trial. You'll receive care from experienced ptsd and trauma-related symptoms 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 ptsd and trauma-related symptoms clinical trials near you to find additional studies recruiting in your area.

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