Clinical trials

2

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Thromboelastography to Study Burn Coagulopathy

This pilot study examines the use of thromboelastography (TEG), a specialized blood test, to evaluate clotting abnormalities in burn patients. The study aims to understand how burn injuries impact the body's ability to form and break down blood clots over time. Specifically, the investigators will research whether the percentage of total body surface area burned (%TBSA) is associated with changes in blood clotting, track the evolution of clotting patterns during the first four weeks following a burn injury, and explore whether these changes can predict recovery or complications. By providing new insights into clotting dynamics in burn patients, the study seeks to improve diagnostic methods, enhance monitoring strategies, and guide treatments to optimize patient care and outcomes.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Francesco EgroUpdated: Mar 17, 2025Locations: 1
Eligibility criteria

Patients admitted with acute burn injuries [+2]

Patients with a history of venous thromboembolism or hyper/hypocoagulopathy

Status: Not yet recruiting

Silver Nitrate vs. Triamcinolone for Treatment of Hypergranulation Tissue

This randomized controlled trial aims to compare the efficacy of silver nitrate, triamcinolone, and a successive use of both treatments in managing hypergranulation tissue in traumatic wounds. Conducted over a four-year period at UPMC Mercy, the study will involve patients presenting with hypergranulation tissue. Participants will be randomly assigned to receive either topical silver nitrate, topical triamcinolone, or a combination of the two in succession. The study will assess treatment outcomes based on the reduction or resolution of hypergranulation tissue, with the goal of identifying the most effective therapeutic approach. This research will provide valuable insights into optimizing treatment strategies for hypergranulation tissue in traumatic wounds.

Participants needed: 270
Trial details
Phase: Phase 2, Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Francesco EgroUpdated: Mar 10, 2025Locations: 1
Eligibility criteria

Patients must be 18 years or older. [+4]

Patients with known allergies or contraindications to silver nitrate or triamcin... [+3]