Clinical trials

4

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

Condition / disease
Location
Status: Recruiting

Laparoscopic Ultrasound Versus Fluorescence Cholangiography in Technically Challenging Laparoscopic Cholecystectomy

This is a multicenter, prospective, interventional clinical trial designed to evaluate and compare two intraoperative imaging modalities: laparoscopic ultrasound (LUS) and fluorescence cholangiography with indocyanine green (ICG), for the identification of biliary anatomy in technically challenging laparoscopic cholecystectomy. All enrolled subjects will undergo both LUS and ICG during the index procedure, following a standardized sequence, in order to allow intra-subject comparison. LUS will be performed first, followed by fluorescence cholangiography prior to Calot's triangle dissection. The primary endpoint is the successful identification of the critical junction. Secondary endpoints include visualization of individual biliary structures, time to visualization, total operative time, intraoperative and postoperative complications.

Participants needed: 62
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Consorci Sanitari IntegralUpdated: Feb 10, 2026Locations: 1
Eligibility criteria

Age ≥ 18 years. [+5]

Known allergy to ICG or iodine. [+7]

Status: Recruiting

Evaluating Residual Congestion at Discharge in Acute Heart Failure Patients

Treatment of congestion is one of the main goals in patients hospitalized for acute heart failure. Nevertheless, current evidence shows that decongestion is often not achieved and that residual congestion at discharge is strongly associated with poor outcomes. While this association has been demonstrated, previous studies have primarily focused on single parameters of congestion (physical examination, biomarkers, or imaging features). The aim of the study is to assess residual congestion at discharge using a multiparametric approach and to compare the prognostic value of each evaluation strategy. Additionally, the analysis will be supported by artificial intelligence to develop a multiparametric prognostic algorithm that can provide an improved predictive model compared to standard statistical approaches.

Participants needed: 500
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Consorci Sanitari IntegralUpdated: Jul 18, 2025Locations: 1
Eligibility criteria

Age ≥ 18 years. [+4]

Known diagnosis of septicemia. [+8]

Status: Not yet recruiting

Prevention of Parastomal Hernias With a Preformed Three-dimensional, Funnel-shaped Mesh

Parastomal hernia (PH) remains a significant complication following stoma creation, boasting a considerable prevalence in the range of 30 to 50% within the first year post-surgery, a figure that climbs even higher when considering radiological evidence irrespective of clinical symptoms. A noteworthy one-third of these cases necessitate subsequent surgical interventions, yielding suboptimal outcomes both in the short and long term. The clinical manifestations of PH are diverse, ranging from mild inconveniences like fecal leakage and dermatitis to more severe and potentially life-threatening complications such as intestinal obstruction, hernia incarceration, and ischemia. Various systematic reviews and meta-analyses have advocated for the adoption of prophylactic meshes, although defining precise incidence and recurrence rates has proven challenging due to methodological disparities across studies. Keyhole and modified Sugarbaker techniques dominate laparoscopic and robotic approaches, yet none offer ideal outcomes. The aim of this study is to evaluate the decrease of postoperative parastomal hernia using this three-dimensional, funnel-shaped mesh.

Participants needed: 58
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Consorci Sanitari IntegralUpdated: Aug 1, 2024Locations: 1
Eligibility criteria

Patients undergoing a definitive colostomy confection [+3]

Lateral colostomy or a colostomy that will be removed posteriorly

Status: Not yet recruiting

Two Hypoabsorption Techniques for the Treatment of Type III Obesity (OASIS)

This study aims to compare the percentage of total weight lost in long-term follow-up after two surgical interventions (SADIS and OAGB) in patients with morbid obesity BMI between 45-49.9.

Participants needed: 96
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Consorci Sanitari IntegralUpdated: Jul 17, 2023
Eligibility criteria

Patients over 18 and under 65 who meet criteria for bariatric surgery. [+3]

Previous bariatric surgery [+4]