Clinical trials

5

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

Condition / disease
Location
Status: Recruiting

Microneurography and Intraneural Microstimulation for Upper Limb Sensory Investigation in Healthy and Amputee Subjects

The goal of this experimental study is to investigate the somatosensory system through intraneural recording and stimulation of the median nerve in healthy volunteers and participants with upper-limb amputation. The main questions it aims to answer are: * How does median nerve activity encode tactile perception during different types of mechanical tactile stimulation in healthy subjects? * How can tactile information be artificially encoded and restored through intraneural microstimulation in both healthy subjects and upper-limb amputee participants? How rich and functionally meaningful is the restored sensory information? * What are the neurophysiological mechanisms underlying tactile stimulus processing and the associated patterns of brain activation during tactile stimulation? Participants will undergo median nerve recordings using microneurography during controlled mechanical tactile stimulation, as well as intraneural microstimulation with specific patterns to evoke near-natural tactile sensations. They will perform perceptual reporting tasks related to stimulus type, intensity, and localization, as well as psychophysical tests under different stimulation conditions. When possible, they will also undergo non-invasive recordings of brain activity using electroencephalography during sensory stimulation.

Participants needed: 100
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: Azienda Ospedaliero, Universitaria PisanaUpdated: Jul 9, 2026Locations: 1
Eligibility criteria

Age between 18-60 years, of any sex [+10]

Conditions affecting perceptual abilities [+23]

Status: Recruiting

Patients With Severe TrIcuspid Regurgitation After triCvALve System Implantation

International Registry to collect patients with severe TR undergoing TricValve implantation from multiple Italian and European centers, aimed at: * Assessing the effect of TricValve implantation on cardiovascular and all-cause mortality, HF rehospitalization, renal function, functional capacity and quality of life. * Clarifying the haemodynamic effects of TricValve implantation and investigating their pathophysiological implications.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Azienda Ospedaliero, Universitaria PisanaUpdated: May 11, 2026Locations: 1Duration: 3 Years
Eligibility criteria

The subject must be 18 years of age or older [+5]

Known significant intracardiac shunt (e.g. ventricular septal defect) or congeni... [+12]

Status: Not yet recruiting

Study in Patients With Osteoporosis and Fragility Fractures to Estimate the Extent and Impact of Delayed Administration of Anti-fracture Therapy

Osteoporosis (OP) and fragility fractures are a significant problem that leads to morbidity, mortality, and high costs for the National Health System. The treatment of fragility fractures includes numerous anti-resorptive and anabolic drugs, and its goal is the secondary prevention of new fractures. It is well known that the risk of a new fracture following a fracture event is highest in the months immediately following the first fracture. However, recent data clearly show a dramatic global delay in the administration of anti-osteoporotic therapy following a fragility fracture. It has been estimated that in Italy, 71% of patients with fragility fractures eligible for anti-fracture treatment did not receive timely treatment (a problem defined as a "treatment gap"), and that in 2034, the incidence of new fragility fractures will increase compared to 2019 \[1\]. However, there is a lack of real-life Italian data on the extent of the treatment gap in osteoporotic patients with fragility fractures and its impact in terms of the incidence of subsequent fragility fractures: this study therefore aims to fill this gap by collecting data from a large population of patients attending several centers throughout the country.

Participants needed: 8,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Azienda Ospedaliero, Universitaria PisanaUpdated: Apr 6, 2026Locations: 1
Eligibility criteria

adult patients of both sexes; [+2]

patients under the age of 18 [+1]

Status: Recruiting

NENCA Study on Neurological Complications of Long COVID-19 in Children and Adolescents; Neurophysiological, Electroencephalographic and Neuroradiological Investigation

The study seeks to investigate the neurological effects caused by Covid-19 in children and adolescents in the 6-16 age group. To do this, neuropsychological scales, an EEG and an MRI were used.

Participants needed: 100
Trial details
Age: 6-16Biological sex: AllType: InterventionalSponsor: Azienda Ospedaliero, Universitaria PisanaUpdated: Mar 14, 2025Locations: 1
Eligibility criteria

Age between 6 years and 16 years and 11 months [+2]

Poor knowledge of the Italian language or other limitation of verbal communicati... [+3]

Status: Recruiting

Serum Calprotectin in Surgical Septic Patients

To early evaluate the serum levels of calprotectin in patients suffering from intra-abdominal sepsis requiring a surgical treatment. The research project aims to investigate the role of serum calprotectin in the diagnosis of sepsis and to establish whether its level significantly correlates with different degree of disease severity and with short and long-term outcomes. If these associations were confirmed, serum calprotectin would represent an easily and rapidly detectable biomarker able to predict the severity of sepsis.

Participants needed: 150
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Azienda Ospedaliero, Universitaria PisanaUpdated: Sep 26, 2024Locations: 1Duration: 6 Months
Eligibility criteria

diagnosis of upper/lower gastro-intestinal perforation [+4]

recent (<3 months) surgery [+3]