Wound Complications

2

Review clinical trials related to Wound Complications. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Closed Incision NPWT to Prevent Wound Complications Post-ECMO

Patients undergoing extracorporeal membrane oxygenation (ECMO) are at increased risk of wound complications at the vascular access site after decannulation. These complications may delay recovery and increase healthcare burden. Closed incision negative pressure wound therapy (NPWT) may improve wound healing by reducing fluid accumulation and supporting the incision. This study evaluates whether prophylactic NPWT reduces wound complications compared to standard wound care following ECMO decannulation.

Participants needed: 144
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: St. Antonius HospitalUpdated: Jul 16, 2026
Eligibility criteria

Patient is aged 18 years or older [+3]

Duration ECMO run < 24 hours [+5]

Status: Not yet recruiting

Clinical Impact of Surgical Wound Morbidity According to the Type of Saphenous Vein Harvesting Technique (Endoscopic vs. Open) in Patients Undergoing Myocardial Revascularization Surgery

The goal of this clinical trial is to compare two different techniques: endoscopic saphenous vein harvesting versus conventional open harvesting in patients undergoing coronary artery bypass grafting, either alone or in combination with another cardiac surgical procedure (valve surgery or arrhythmia surgery). The main questions the trial aims to answer are: Does the endoscopic technique reduce surgical wound morbidity in terms of shorter hospital stays? Does endoscopic saphenous harvesting reduce the use of antibiotics for saphenectomy wound infections? Does the endoscopic technique reduce need for wound dressings due to necrosis and/or wound infection, and reduce need for analgesic treatment for wound pain? This prospective, randomized study will be conducted in the Cardiovascular Surgery Service at Hospital Clínico San Carlos. Participants will be randomly assigned to a different saphenectomy technique. All patients will be assessed for saphenectomy wound complications upon discharge, and by phone call at 7 days, 1 month, and 3 months following the intervention.

Participants needed: 356
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Hospital San Carlos, MadridUpdated: Jun 6, 2025Locations: 1
Eligibility criteria

Patients undergoing coronary artery bypass grafting (CABG), alone or in combinat... [+3]

Emergent surgery or procedures performed during cardiorespiratory arrest [+9]