War-Related Injuries

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Review clinical trials related to War-Related Injuries. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

ASV and Targeted Fluid Resuscitation in Severe Burns

This prospective cohort study will evaluate the use of Adaptive Support Ventilation (ASV) together with targeted fluid resuscitation in adult patients with severe burn injuries requiring mechanical ventilation in the intensive care unit. Patients with extensive burns often develop respiratory failure and require both invasive mechanical ventilation and large-volume fluid resuscitation during the first days after injury. The study will assess whether the combination of ASV and targeted fluid resuscitation is associated with improved oxygenation, respiratory mechanics, fluid balance, and early clinical outcomes during the first 72 hours of intensive care. Clinical data, ventilatory parameters, laboratory results, hemodynamic variables, and fluid resuscitation characteristics will be collected as part of routine clinical care. The findings may help optimize early intensive care management for patients with severe burn injuries and improve future treatment strategies.

Participants needed: 100
Trial details
Age: 18-50Biological sex: AllType: ObservationalSponsor: Ukrainian Society of Regional Anesthesia and Pain TherapyUpdated: Jul 8, 2026Locations: 1Duration: 7 Days
Eligibility criteria

Adults aged 18 years or older. [+5]

Age younger than 18 years. [+8]

Status: Recruiting

Confirming the Effects of Acupuncture Treatments to Relieve Symptoms of Gulf War Illness

This unblinded Phase II clinical trial will test the effects of individualized acupuncture treatments offered in extant acupuncture practices in the community; practitioners will have had at least 5 years of experience plus additional training provided by the study. Veterans with diagnosed symptoms of Gulf War Illness will be randomized to either six months of biweekly acupuncture treatments (group 1, n=100) or 2 months of waitlist followed by weekly acupuncture treatments (group 2, n=100). Measurements were taken at baseline, 2, 4 and 6 months. The primary outcome is the SF-36 physical component scale score (SF-36P).

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of UtahUpdated: Apr 3, 2026Locations: 10
Eligibility criteria

Deployed to the Gulf Theater of operations (as defined by 38 CFR 3.317, includes...

Currently enrolled in another clinical trial [+3]

Status: Not yet recruiting

From Battlefield to Recovery: Continuous Regional Anaesthesia for War-Related Lower Limb Trauma

To compare the effectiveness of continuous regional anaesthesia with standard pain management strategies for the treatment of acute pain in patients with war-related lower limb trauma.

Participants needed: 150
Trial details
Age: 18-50Biological sex: AllType: ObservationalSponsor: Charitable Organisation Charitable Fund Superhumans (Co Cf Superhumans)Updated: Mar 17, 2026Locations: 1Duration: 6 Weeks
Eligibility criteria

age ≥18 years [+5]

age <18 years [+4]