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Centre Hospitalier Universitaire Vaudois Clinical Trials

Studies where Centre Hospitalier Universitaire Vaudois is the lead sponsor: what is enrolling now, by phase, condition and country.

208 registered studies

In numbers

Open to volunteers
34
Active
40
With results posted
4
All registered
208

Open to volunteers: recruiting, not yet recruiting or enrolling by invitation. Active adds studies under way that have stopped recruiting.

Open to volunteers

All 34
  • Autism Spectrum Disorder

    Impact of an E-Learning Coaching for Parents of Young Children With Autism

    • Recruiting
    • Age: 24 to 48 months
    • Lifestyle or therapy programme

    The goal of this study is to evaluate the impact of a parental coaching based on E-Learning (EL), intended for parents of children with autism spectrum disorder (ASD).

    Trial name
    ECOACH (NCT05726708)
    Testing
    E-Learning
    Where
    Switzerland
    Volunteers
    99 people
    Sponsor
    Centre Hospitalier Universitaire Vaudois
    Can I take part? ECOACH
  • Rheumatic Disorder, Rheumatoid Arthritis (RA)

    DETECTRA: Remote Monitoring to Detect Rheumatoid Arthritis Flares and Treatment Response

    • Not yet recruiting
    • Age: 18 to 80 years
    • Medical device

    The goal of this clinical trial is to learn if the DETECTRA remote monitoring platform can help clinicians detect rheumatoid arthritis (RA) disease flares earlier and more reliably, as well as identify response and non-response…

    Trial name
    Pix-Monitor (NCT07857993)
    Testing
    DETECTRA, Standard of Care (SOC)
    Where
    3 sites in Austria, Germany
    Volunteers
    320 people
    Sponsor
    Centre Hospitalier Universitaire Vaudois
  • Rheumatoid Arthritis (RA

    Pix-Risk: Early Detection of Rheumatoid Arthritis Via the DETECTRA Platform

    • Not yet recruiting
    • Age: 18 years and older
    • Medical device

    The goal of this clinical trial is to learn if a remote monitoring application called DETECTRA can help doctors diagnose rheumatoid arthritis earlier in people who are at risk of developing the disease.

    Trial name
    Pix-Risk (NCT07825233)
    Testing
    DETECTRA, Standard of Care (SOC)
    Where
    5 sites in Austria, Denmark and 2 more
    Volunteers
    142 people
    Sponsor
    Centre Hospitalier Universitaire Vaudois
    Can I take part? Pix-Risk
  • Pain After Shoulder Surgery

    Analgesic Efficacy of the Infraspinatus-Teres Minor (ITM) Interfascial Plane Block After Shoulder Arthroscopy: A Simon's Two-Stage Design

    • Not yet recruiting
    • Age: 18 years and older

    The main study objective is to observe the ability of the ITM block to provide clinically acceptable pain control after elective shoulder arthroscopy as measured by pain scores and morphine consumption.

    Trial name
    ITM (NCT07808008)
    Testing
    Infraspinatus-teres minor block
    Where
    Switzerland
    Volunteers
    29 people, healthy volunteers welcome
    Sponsor
    Centre Hospitalier Universitaire Vaudois
    Can I take part? ITM
  • Vexas Syndrome

    Clinical Phenotype and Prevalence of VEXAS Syndrome in Internal Medicine

    • Not yet recruiting
    • Age: 50 years and older
    • Observational study

    The FIND-VEXAS project is a multicenter, cross-sectional observational study conducted in Internal Medicine departments in the Friuli Venezia Giulia region of Italy.

    Trial name
    FIND-VEXAS (NCT07708688)
    Testing
    UBA1 Genetic Testing
    Volunteers
    50 people
    Sponsor
    Centre Hospitalier Universitaire Vaudois
    Can I take part? FIND-VEXAS
  • Post Operative Analgesia, Rebound Pain

    Prevention of Rebound Pain After Orthopaedic Surgery With Peripheral Nerve Block (REBOUND)_part B

    • Not yet recruiting
    • Age: 18 years and older
    • Pill or oral medicine

    Rebound pain after peripheral nerve blocks reduces the benefits of regional anesthesia and increases opioid consumption. This rebound pain most likely results from suboptimal pain management, as patients receiving a peripheral…

    Conditions
    Post Operative Analgesia, Rebound Pain, Post Operative Pain, Acute
    Trial name
    REBOUND (NCT07666009)
    Testing
    Morphine provided via oral PCA, Morphine provided via oral PCA + morphine administered at a scheduled regimen
    Where
    Switzerland
    Volunteers
    100 people
    Sponsor
    Centre Hospitalier Universitaire Vaudois
    Can I take part? REBOUND
  • Post Operative Analgesia, Rebound Pain

    Prevention of Rebound Pain After Orthopaedic Surgery With Peripheral Nerve Block (REBOUND)_part A

    • Not yet recruiting
    • Age: 18 years and older
    • Pill or oral medicine

    Rebound pain after peripheral nerve blocks reduces the benefits of regional anesthesia and increases opioid consumption. This rebound pain most likely results from suboptimal pain management, as patients receiving a peripheral…

    Conditions
    Post Operative Analgesia, Rebound Pain, Post Operative Pain, Acute
    Trial name
    REBOUND (NCT07666971)
    Testing
    Morphine provided via oral PCA, Morphine provided via oral PCA + morphine administered at a scheduled regimen
    Where
    Switzerland
    Volunteers
    100 people
    Sponsor
    Centre Hospitalier Universitaire Vaudois
    Can I take part? REBOUND
  • Advanced Melanoma, Melanoma Metastatic

    NY-ESO-1-redirected T Cells in Patients With Advanced Melanoma and Sarcoma

    • Recruiting
    • Age: 18 years and older
    • Phase 1
    • Surgery or procedure

    A single center, dose escalaion, Phase I clinical trial to demonstrate safety and efficacy of LauT-1, autologous "New York Esophageal Squamous Cell Carcinoma-1 T-Cell Receptor (NY-ESO-1 TCR)-directed T cells in combination with…

    Conditions
    Advanced Melanoma, Melanoma Metastatic, Sarcoma
    Trial name
    LauT1 (NCT06889766)
    Testing
    NY-ESO-1 TCR redirected autologous T cell product, Low-dose irradiation, Non-myeloablative lymphodepleting chemotherapy
    Where
    2 sites in Switzerland
    Volunteers
    9 people
    Sponsor
    Centre Hospitalier Universitaire Vaudois
    Can I take part? LauT1
  • Obstructive Sleep Apnea (OSA), Insomnia Chronic

    Effective of Early Treatment of Insomnia on the Adherence of CPAP

    • Not yet recruiting
    • Age: 45 to 65 years
    • Medical device
    • Lifestyle or therapy programme

    This study includes patients suffering from both sleep apnea and insomnia. All participants receive treatment with CPAP. Half of the participants additionally receive a digital program to treat insomnia, initiated at the same…

    Trial name
    CoPAP (NCT07556432)
    Testing
    digital CBT-I, CPAP
    Volunteers
    120 people
    Sponsor
    Centre Hospitalier Universitaire Vaudois
    Can I take part? CoPAP
  • N1/N2b Oral Cavity Cancer, Head and Neck Skin Cancer

    Prospective Clinical Study to Identify Secondary Sentinel Lymph Nodes in Patients With N1/N2b Oral Cavity or H&N Skin Cancers Using Patent Blue V and Indocyanine Green Dyes

    • Not yet recruiting
    • Age: 18 years and older
    • Phase 2
    • Injection or infusion

    Head and neck (H\&N) cancer has a poor prognosis and high morbidity with ~50% survival and frequent treatment resistance. Most deaths result from local or loco-regional progression rather than distant metastasis.

    Trial name
    preReDSeL (NCT07518485)
    Testing
    Patent blue V dye injection, Indocyanine green dye injection
    Where
    2 sites in Switzerland
    Volunteers
    20 people
    Sponsor
    Centre Hospitalier Universitaire Vaudois
    Can I take part? preReDSeL

Completed, with results posted

All 3
  • Melanoma

    Immunotherapy of Stage III/IV Melanoma Patients

    • Completed
    • Age: 18 years and older
    • Phase 1
    • Results posted

    The purpose of this study is to determine whether vaccination with melanoma antigen peptides [Melan-A/Mart-1 (both EAA and ELA), NY-ESO-1b analog, Long NY-ESO-1 LP and MAGE-A10] and Montanide, CpG adjuvants and low dose rIL-2 can…

    Trial name
    NCT00112242
    Testing
    Melan-A ELA + Montanide, Melan-A ELA + NY-ESO-1b + MAGE-A10 + Montanide, Melan-A -ELA + NY-ESO-1b + MAGE-A10 peptide + Montanide + CpG
    Where
    2 sites in Switzerland
    Volunteers
    39 people
    Sponsor
    Centre Hospitalier Universitaire Vaudois
    Can I take part? NCT00112242
  • Hypertension

    Effect of Aliskiren and Hydrochlorothiazide on Kidney Oxygenation in Patients With Hypertension

    • Completed
    • Age: 18 years and older
    • Phase 4
    • Results posted

    The goal of this project is to evaluate the chronic effect (8 weeks) of RASILEZ 300mg (aliskiren) on renal tissue oxygenation in patients with stage 1-2 hypertension, and to compare the chronic effect (8 weeks) of RASILEZ 300mg…

    Trial name
    NCT01519635
    Testing
    Aliskiren, Hydrochlorothiazide
    Where
    Switzerland
    Volunteers
    24 people, healthy volunteers welcome
    Sponsor
    Centre Hospitalier Universitaire Vaudois
    Can I take part? NCT01519635
  • Skin Graft

    Effect of Platelet Rich Plasma and Keratinocyte Suspensions on Wound Healing

    • Completed
    • Age: 18 to 80 years
    • Phase 1
    • Results posted

    This prospective randomized trial evaluated the impact of autologous keratinocytes suspended in platelet concentrates on healing skin graft donor site wounds.

    Trial name
    NCT00856934
    Testing
    Autologous Platelet Rich Plasma, Keratinocyte suspension, Standard dressings
    Where
    Switzerland
    Volunteers
    45 people
    Sponsor
    Centre Hospitalier Universitaire Vaudois

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