Clinical trials

14

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

Condition / disease
Location
Status: Recruiting

Real-Time Monitoring of the Injection Pressure During the Peripheral Nerve Block

The goal of this clinical trial with medical device is to learn if the Smart Needle Monitoring System works to maintain a safe low injection pressure during a type of regional anaesthetic (Peripheral Nerve Block (PNB)) in patients due to undergo surgery below the elbow . It will also learn about the safety of the device and patients' perception of the quality of anesthesia. Participants will: * be operated locally according to standard clinical practice * undergo post-anesthesia recovery and any neurologic symptoms or signs assessment on postoperative days 1 and 7

Participants needed: 34
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Ente Ospedaliero Cantonale, BellinzonaUpdated: Mar 13, 2026Locations: 1
Eligibility criteria

Informed Consent signed by the subject [+5]

Contraindications to the axillary block (e.g., local infection) [+5]

Status: Recruiting

Quality of Postoperative Analgesia and Functional Recovery After Elective Cesarean Delivery

Based on randomization, patients will receive a mixture for spinal anesthesia and will be followed in the following hours for the various outcomes and for functional recovery

Participants needed: 63
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Ente Ospedaliero Cantonale, BellinzonaUpdated: Mar 16, 2026Locations: 1
Eligibility criteria

patients over 18 year of age [+4]

patients with inability to consent [+5]

Status: Recruiting

AI-assisted Migraine Education: Efficacy, Safety and Patients' Acceptance

Migraine affects 1 in 7 people globally, significantly impacting quality of life and economic productivity. Despite its prevalence, limited awareness leads to misdiagnosis, inadequate treatment, and stigmatization. AI can enhance migraine management through improved diagnosis, prediction, and personalized education. The primary objective of this study is to determine if adding AI-assisted migraine education to standard education improves patients' understanding of their condition more effectively.

Participants needed: 140
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Ente Ospedaliero Cantonale, BellinzonaUpdated: Mar 12, 2026Locations: 1
Eligibility criteria

aged between 18 and 65 years at the time of signing the informed consent [+3]

Insufficient knowledge of the protocol language (italian) [+2]

Status: Recruiting

This is a Study to Find Out Whether Music Therapy Can Reduce Stress During Wound Care

This study involves hospitalized patients who need wound dressing procedures. Patients will be assigned by chance to one of two groups. One group will listen to music of their choice during wound care, while the other group will receive standard wound care without music. The investigators will then compare the two groups to see whether listening to music helps reduce stress and improve the experience during the procedure.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Ente Ospedaliero Cantonale, BellinzonaUpdated: Mar 10, 2026Locations: 1
Eligibility criteria

Hospitalized patients undergoing wound dressing procedures [+1]

Pregnant or lactating women [+3]

Status: Recruiting

This is a Study to Verify if Periarticular Hip Injection of Corticosteroid After Hip Replacement Reduce the Pain and the Hospitalisation Time

The investigators are going to evaluate if periarticular corticosteroid injection during endoprothesis implantation can lead to any advantage to the patients, namely if it can reduce post-operative pain, lenght and cost of hospitalisation, use of analgesics drugs.

Participants needed: 110
Trial details
Phase: Phase 4Age: 50-90Biological sex: AllType: InterventionalSponsor: Ente Ospedaliero Cantonale, BellinzonaUpdated: Mar 5, 2026Locations: 1
Eligibility criteria

Patients undergoing unilateral cemented hip endoprosthesis for femoral neck frac... [+4]

Contraindications to steroids [+12]

Status: Recruiting

Effect of Virtual Reality on the Need of Premedication Before Surgery

This study will assess, on patients requesting a pharmacological premedication in the preoperative period, if virtual reality reality could reduce the request of pharmacological premedication while maintaining a good level of comfort for the patient. The aim of this study is to understand if virtual reality could reduce the need for pharmacological premedication and their associated secondary effects.

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Ente Ospedaliero Cantonale, BellinzonaUpdated: Mar 4, 2026Locations: 1
Eligibility criteria

All patients undergoing elective surgery [+3]

Lacking capacity or ability to complete the consent form or to respond to the re... [+10]

Status: Recruiting

This is a Study to Find Out Whether Surgery Using a Metal Plate to Fix a Broken Elbow in Older Adults Leads to Better Recovery and Arm Function Compared to Non-surgical Treatment

This study takes place in one hospital and uses a random method to divide patients into groups. It looks at the best way to treat a broken elbow (specifically, a displaced olecranon fracture) in older adults who don't use their arms heavily. There are 84 patients in total, with 42 people in each group

Participants needed: 84
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: Ente Ospedaliero Cantonale, BellinzonaUpdated: Feb 10, 2026Locations: 1
Eligibility criteria

Patients with an acute (< 2 weeks) Mayo type 2A or 2B olecranon fracture [+3]

Patients aged < 65 years or with a Clinical Frailty Scale score > 7 or < 2 [+8]

Status: Recruiting

A Study to Compare Two Different Managements After Ankle Surgery: Immediate and Delayed Weight-bearing.

The investigators will compare two types of rehabilitation in patients who undergo a surgery for treatment of malleolar fractures: immediate complete weight-bearing and delayed weight-bearing. The investigators want to evaluate if the immediate complete weight-bearing can improve and hasten the functional outcome of the ankle without increasing the risk of complications.

Participants needed: 100
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: Ente Ospedaliero Cantonale, BellinzonaUpdated: Aug 7, 2025Locations: 1
Eligibility criteria

Male and female adults [+4]

Weber C fracture pattern [+9]

Status: Recruiting

This is a Study to Evaluate a Pre-confectioned Plantar Insole for the Treatment of Plantar Heel Pain

Patients affected by plantar heel pain will be asked to use a pre-confectioned plantar insole for one year. The aim of the study is to assess if the insole under study allows the patient to reach a better mobility and a faster return to the normal everyday life.

Participants needed: 25
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: Ente Ospedaliero Cantonale, BellinzonaUpdated: Aug 6, 2025Locations: 1
Eligibility criteria

Age ranging 18 to 70 years [+3]

Diabetes mellitus not controlled pharmacologically [+3]

Status: Recruiting

Comparing Reports Recorded by the Patients at the Time at Which They Feels Pain to What Patients Report at Monthly Visits to Assess Symptoms of Musculoskeletal Diseases.

Patients will be introduced to the use of a mobile application for their smartphone to record the Ecological Momentary Assessment (EMA). This app will ask the patients to assess their pain and function two times daily for 2 months. After 1 month and at the end of the 2 months, follow-up visits will be performed and patients will be asked to retrospectively evaluate the pain that they suffered and the level of function they had during the last month.

Participants needed: 1,500
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Ente Ospedaliero Cantonale, BellinzonaUpdated: Aug 6, 2025Locations: 2
Eligibility criteria

Symptomatic patients [+4]

Patients unable to follow the protocol of the study (i.e. unable to use a smartp... [+6]

Status: Recruiting

This is a Study to Evaluate Nanofractures Technique in the Treatment of Cartilage Lesions

Articular cartilage lesions, with their inherent limited healing potential, remain a challenging problem for orthopaedic surgeons. Various techniques, both palliative and reparative, have been used to treat this injury with variable success rates. If not adequately treated, they may even lead to the development of early-onset osteoarthritis. Among all the available techniques, microfractures are used in restoring the cartilage tissue, especially in the deep and extended lesions. More recently, the need for minor bone trauma with still adequate bleeding resulted in the development of nanofractures. Nanofracturing means creating perforations with a smaller diameter that go deeper into the bone while damaging it less. This is supposed to reduce the injury to the subchondral bone and increase the amount of bone marrow-derived mesenchymal stromal cells at the bone surface. Thus, the aim of this pilot study is to evaluate the efficacy of nanofractures for the treatment of cartilage lesions of the knee, specifically focusing on the chondral healing that will be addressed with magnetic resonance imaging.

Participants needed: 20
Trial details
Age: 16-50Biological sex: AllType: InterventionalSponsor: Ente Ospedaliero Cantonale, BellinzonaUpdated: Aug 6, 2025Locations: 1
Eligibility criteria

Patients with cartilage lesions of the knee scheduled for surgery [+3]

Uncorrected knee instability [+4]

Status: Recruiting

Total Hip Arthroplasty: Fluoroscopy vs Freehand

The aim of the study is to compare total hip arthroplasty intervention executed with or without the use of intraoperative fluoroscopy in terms of positioning of the hip prosthesis. The comparison will be made on post-operative follow-up X-ray performed as per clinical practice, in order to verify if intraoperative fluoroscopy provides better prosthesis components positioning or not.

Participants needed: 84
Trial details
Age: 18-90Biological sex: AllType: InterventionalSponsor: Ente Ospedaliero Cantonale, BellinzonaUpdated: Aug 8, 2025Locations: 1
Eligibility criteria

Patients undergoing unilateral primary THA through DAA [+4]

Revision THA. [+4]

Status: Recruiting

A Study to Compare Early and Partial Weight-bearing After Hallux Valgus Surgery

This is a two-arm randomized controlled trial with the aim to evaluate the effectiveness and safety of post-operative management after a modified Lapidus arthrodesis with/without an Akin or a Weil/Hohmann surgery fusion with immediate complete weight-bearing compared with partial weight-bearing (10 - 15kg) for 6 weeks as a novel approach for rehabilitation after a foot surgery.

Participants needed: 122
Trial details
Age: 18-85Biological sex: AllType: InterventionalSponsor: Ente Ospedaliero Cantonale, BellinzonaUpdated: Aug 6, 2025Locations: 1
Eligibility criteria

Additional surgical gestures such as e.g. interventions on the proximal phalanx... [+2]

Diabetes mellitus [+6]

Status: Recruiting

Ultrasound Evaluation of Superior Mesenteric Artery Measurements in a Healthy Pediatric Population

Multicenter, prospective, observational research project on children aged from 10 to 15 years old undergoing abdominal ultrasound examinations during routine clinical practice.

Participants needed: 289
Trial details
Age: 10-15Biological sex: AllType: ObservationalSponsor: Ente Ospedaliero Cantonale, BellinzonaUpdated: Jul 31, 2025Locations: 2
Eligibility criteria

Male and female children [+3]

Presence of a disease that could distort the anatomy around the SMA (e.g., abdom... [+1]