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Condition

Trauma Clinical Trials

Studies of trauma, matched by condition name and medical subject headings. Start with those open to enrolment.

2,022 registered studies

In numbers

Open to volunteers
414
Active
477
With results posted
148
All registered
2,022

Open to volunteers: recruiting, not yet recruiting or enrolling by invitation. Active adds studies under way that have stopped recruiting.

Open to volunteers

All 414
  • Urologic Diseases, Male Urogenital Diseases

    Bioengineered Penile Tissue Constructs for Irreversibly Damaged Penile Corpora

    • Not yet recruiting
    • Age: 18 to 60 years
    • Phase 1

    The primary objective of this clinical trial is to evaluate the safety of autologous engineered corpora cavernosa + albuginea constructs for treatment of complex penile deformities.

    Conditions
    Urologic Diseases, Male Urogenital Diseases, Penile Diseases, Corpus Callosum Malformation
    Trial name
    NCT03463239
    Testing
    Autologous tissue engineered corpora
    Where
    United States
    Volunteers
    10 people
    Sponsor
    Wake Forest University Health Sciences
    Can I take part? NCT03463239
  • Acute Spinal Cord Injury (SCI), Spinal Cord Diseases

    NG004 in Incomplete Spinal Cord Injury Patients

    • Recruiting
    • Age: 18 to 75 years
    • Phase 1
    • Injection or infusion

    This is a randomized, double-blind, placebo controlled, multicenter trial of NG004 in patients with acute traumatic incomplete cervical SCI.

    Conditions
    Acute Spinal Cord Injury (SCI), Spinal Cord Diseases, Spinal Cord Injuries, Trauma Nervous System
    Trial name
    SPROUT-2 (NCT07840196)
    Testing
    NG004
    Where
    10 sites in Germany, Switzerland
    Volunteers
    120 people
    Sponsor
    NovaGo Therapeutics AG
    Can I take part? SPROUT-2
  • Burnout, Secondary Trauma

    PATH to Reducing Burnout Among Peers Who Deliver Overdose Prevention Services (R33 Phase Clinical Trial)

    • Enrolling by invitation
    • Age: 18 years and older
    • Lifestyle or therapy programme

    The investigators propose to test the effectiveness of PATH (Peer Advanced Training for total Health) as an educational workforce intervention for improving peer recovery support specialists' (PRSS) overdose prevention (OP)…

    Conditions
    Burnout, Secondary Trauma, Compassion Fatigue, Opioid Use Disorder
    Trial name
    NCT07886944
    Testing
    PATH (Peer Advanced Training for total Health)
    Where
    United States
    Volunteers
    200 people
    Sponsor
    Chestnut Health Systems
    Can I take part? NCT07886944
  • Ocular Trauma

    Corneal Trauma Diagnostic Study

    • Recruiting
    • Age: 18 years and older

    Tear fluid will be collected from patients diagnosed with ocular trauma at the University of Pittsburgh Medical Center to evaluate biomarkers.

    Trial name
    NCT07887425
    Testing
    Tear fluid collection with mass spec analysis.
    Where
    United States
    Volunteers
    40 people
    Sponsor
    InnSight Technology, Inc.
    Can I take part? NCT07887425
  • Septic Shock, Acute Respiratory Distress Syndrome

    CytOSorb TreatMent Of Critically Ill PatientS Registry

    • Recruiting
    • Age: All ages
    • Observational study
    • Medical device

    Registry intended to provide a data repository and reporting infrastructure for the surveillance of CytoSorb device use in real-world critical care settings, and to serve as an objective, comprehensive, and scientifically-based…

    Conditions
    Septic Shock, Acute Respiratory Distress Syndrome, Trauma, Rhabdomyolysis
    Trial name
    COSMOS (NCT05146336)
    Testing
    CytoSorb
    Where
    28 sites in Austria, Germany and 4 more
    Volunteers
    3,000 people
    Sponsor
    CytoSorbents, Inc
    Can I take part? COSMOS
  • Head Injury Trauma, Traumatic Brain Injury, Mild

    The PIONEER Comparative Effectiveness Study - Project 2

    • Not yet recruiting
    • Age: 18 years and older

    This is a pragmatic, open-label, multicenter, stepped-wedge, Type II hybrid effectiveness-implementation study. It is designed to evaluate both the comparative effectiveness and implementation feasibility of a…

    Trial name
    NCT07829107
    Testing
    Clinical pathway 1: Guidelines plus biomarkers, Clinical guidelines only
    Where
    6 sites in United States
    Volunteers
    3,000 people
    Sponsor
    University of Michigan
    Can I take part? NCT07829107
  • Trauma Associated Hemorrhage

    Prehospital Transfusion Outcomes in Traumatic Hemorrhage: a Prospective Cohort Study

    • Not yet recruiting
    • Age: 16 years and older
    • Observational study

    Traumatic injuries can cause severe bleeding, which causes a lot of deaths worldwide that could be prevented. Starting treatment as early as possible has been shown to improve survival, which makes fast care very important.

    Trial name
    PRONTO (NCT07883252)
    Where
    Netherlands
    Volunteers
    750 people
    Sponsor
    Erasmus Medical Center
    Can I take part? PRONTO
  • Intergenerational Trauma

    Child Cognitive-Affective Resilience Following 13-11 Event : A Pluridisciplinary Study of Intergenerational Transmission of a Traumatic Event

    • Recruiting
    • Age: 9 years and older
    • Lifestyle or therapy programme

    CARE 13-11 study explores the transmission of trauma within families. Exposure to a traumatic event can have an impact on those directly exposed, but also on their family.

    Trial name
    CARE 13-11 (NCT07203443)
    Testing
    MRI, Psychological assessment, Cognitive assessment
    Where
    France
    Volunteers
    960 people, healthy volunteers welcome
    Sponsor
    Institut National de la Santé Et de la Recherche Médicale, France
    Can I take part? CARE 13-11
  • Nerve Block, Nerve Blocks

    Blast-related Regional Anaesthesia and Peripheral nerVe Injury Evaluation

    • Not yet recruiting
    • Age: 18 to 50 years
    • Injection or infusion
    • Surgery or procedure

    This randomized study will examine whether ultrasound-guided regional anaesthesia (a nerve block) contributes to new or worsening peripheral nerve problems after blast-related limb trauma.

    Conditions
    Nerve Block, Nerve Blocks, Nerve Injury, Blast Injury
    Trial name
    BRAVE (NCT07879508)
    Testing
    Standardized Multimodal Analgesia, Ultrasound-Guided Regional Anaesthesia
    Volunteers
    150 people
    Sponsor
    Ukrainian Society of Regional Anesthesia and Pain Therapy
    Can I take part? BRAVE
  • Spinal Cord Injuries, Neuropathic Pain

    Neuropathic Pain and Operant Conditioning of Cutaneous Reflexes After SCI

    • Recruiting
    • Age: 18 years and older
    • Lifestyle or therapy programme

    The purpose of the second part of the study is to examine the effect of reflex training in the leg to decrease neuropathic pain.

    Conditions
    Spinal Cord Injuries, Neuropathic Pain, Neurological Injury, Pain
    Trial name
    NCT05492188
    Testing
    Operant Conditioning of Cutaneous Reflexes
    Where
    United States
    Volunteers
    15 people
    Sponsor
    Medical University of South Carolina
    Can I take part? NCT05492188

Completed, with results posted

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