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Research institution

University Hospital, Basel, Switzerland Clinical Trials

Studies where University Hospital, Basel, Switzerland is the lead sponsor: what is enrolling now, by phase, condition and country.

990 registered studies

In numbers

Open to volunteers
177
Active
215
With results posted
6
All registered
990

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

Open to volunteers

All 177
  • Atrial Fibrillation (AF)

    A Comparison of Beta-blockers and Calcium Channel Blockers in Atrial Fibrillation

    • Not yet recruiting
    • Age: 18 years and older
    • Phase 4

    Beta-blockers are generally prescribed for the treatment of atrial fibrillation. Their purpose is to slow the heart rate and thereby reduce the workload on the heart.

    Trial name
    BRACE-AFib (NCT07904507)
    Testing
    Experimental intervention, Control Intervention
    Where
    Switzerland
    Volunteers
    266 people
    Sponsor
    University Hospital, Basel, Switzerland
    Can I take part? BRACE-AFib
  • Anastomotic Leaks

    Surgical Intuition in Anastomotic Leakage After Colorectal Surgery

    • Recruiting
    • Age: 18 years and older
    • Observational study

    The SURGUT study aims to assess how well a computer model predicts bowel leaks after surgery. It will also examine whether adding surgeons' intuition improves these predictions.

    Trial name
    SURGUT (NCT07888478)
    Where
    2 sites in Switzerland
    Volunteers
    4,300 people
    Sponsor
    University Hospital, Basel, Switzerland
    Can I take part? SURGUT
  • Lymphedema, Breast Cancer

    The LYMPH Trial - Microsurgical Versus Conservative Treatment of Chronic Breast Cancer Associated Lymphedema

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

    The aim of this study is to test whether lymphatic surgery provides better QoL (assessed with the Lymph-ICF-UL, (Lymphedema Functioning Disability and health questionnaire for upper limb lymphedema)) 15 months after randomization…

    Trial name
    LYMPH (NCT05890677)
    Testing
    Surgical Intervention, Conservative Complex Physical Decongestion Therapy
    Where
    36 sites in United States, Austria and 13 more
    Volunteers
    280 people
    Sponsor
    University Hospital, Basel, Switzerland
    Can I take part? LYMPH
  • Benign Prostate Obstruction (BPO)

    SteamOne - Prospective Database for Rezum Water Vapor Therapy of the Prostate

    • Recruiting
    • Age: 18 years and older
    • Observational study

    This study is to assess the clinical data of Rezum (water vapor therapy) in patients with BPO (benign prostate obstruction) and male LUTS (lower urinary tract symptoms) in terms of efficacy, durability and safety in a large…

    Trial name
    SteamOne (NCT05495633)
    Testing
    Collection and evaluation of clinical (CROMs) and patient-reported outcomes (PROMs), Analysis of uroflowmetry data by EmanoFlow Mobile Application (App) and Emano Clinic Portal
    Where
    19 sites in Austria, Germany and 1 more
    Volunteers
    1,000 people
    Sponsor
    University Hospital, Basel, Switzerland
    Can I take part? SteamOne
  • Carcinoma, Squamous Cell of Head and Neck HNSCC

    Safety and Efficacy of Ruxolitinib in Patients With HNSCC and High NLR Treated With Pembrolizumab - The Phase 2 InflammaSTOP Trial

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

    The goal of this Phase 2 clinical trial is to learn if adding ruxolitinib to pembrolizumab may improve treatment outcomes in patients with head and neck squamous cell carcinoma (HNSCC) who have increased levels of systemic…

    Trial name
    InflammaSTOP (NCT07840456)
    Testing
    Ruxolitinib, Pembrolizumab
    Where
    10 sites in Germany, Switzerland
    Volunteers
    66 people
    Sponsor
    University Hospital, Basel, Switzerland
  • Breast Cancer

    Axillary Radiotherapy or Axillary Lymph Node Dissection in Patients With Clinically Node- Positive Breast Cancer Undergoing Upfront Tailored Axillary Surgery

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

    This trial is to investigate if in patients with clinically node positive breast cancer undergoing upfront surgery, treatment with TAS and ART is superior to ALND in terms of arm-related Quality of Life (QoL) and occurrence of…

    Trial name
    OPBC-10/ NOAX (NCT07140172)
    Testing
    Axillary lymph node dissection (ALND), Axillary radiotherapy (ART)
    Where
    55 sites in United States, Austria and 9 more
    Volunteers
    1,060 people
    Sponsor
    University Hospital, Basel, Switzerland
  • 5-methoxy-dimethyltryptamine (5-MeO-DMT)

    Acute Effects of Intravenous 5-MeO-DMT in Healthy Participants

    • Recruiting
    • Age: 25 to 65 years
    • Phase 1

    Participation in this study lasts approximately two weeks and includes three on-site study visits: a screening visit (approximately 2 hours), a study drug administration visit (approximately 4 hours), and a follow-up visit…

    Trial name
    MEOS (NCT07444788)
    Testing
    0.2 mg/min 5-MeO-DMT, 0.4 mg/min 5-MeO-DMT, 0.6 mg/min 5-MeO-DMT
    Where
    Switzerland
    Volunteers
    40 people, healthy volunteers welcome
    Sponsor
    University Hospital, Basel, Switzerland
    Can I take part? MEOS
  • Perioperative Myocardial Injury

    Incidence and Outcome of Perioperative Myocardial Injury After Non-cardiac Surgery

    • Recruiting
    • Age: 45 years and older
    • Observational study

    This observational study includes patients undergoing major non-cardiac surgery, and screens them for the occurrence of perioperative myocardial injuries (PMI).

    Trial name
    BASEL-PMI (NCT02573532)
    Where
    Switzerland
    Volunteers
    19,645 people
    Sponsor
    University Hospital, Basel, Switzerland
    Can I take part? BASEL-PMI
  • Acute Heart Failure, Acute Coronary Syndrome

    Heart Failure-USB: Prediction and Progression

    • Recruiting
    • Age: 18 years and older
    • Observational study

    This retrospective cohort study is to identify triggers of heart failure (HF) development and drivers of HF progression as well as the underlying cardiac disease (phenotype) to identify patients at risk and predict the clinical…

    Trial name
    HF-USB (NCT04000061)
    Testing
    medical chart review, data generated by direct IT export
    Where
    Switzerland
    Volunteers
    6,000 people
    Sponsor
    University Hospital, Basel, Switzerland
    Can I take part? HF-USB
  • Quality of Life (QOL), Mismatch Repair Deficient Colorectal Cancer

    Research on Effective Strategies After Immunotherapy for Mismatch Repair-deficient Early-stage GI Tumors

    • Recruiting
    • Age: 18 years and older
    • Observational study

    This cohort study is divided into two parts: Part A: Registry Cohort All patients with non-metastatic, MMRd/MSI-H colorectal cancers (and other gastrointestinal cancers for exploratory analysis) who have signed the general…

    Conditions
    Quality of Life (QOL), Mismatch Repair Deficient Colorectal Cancer, Microsatellite Instability-High Colorectal Cancer, Stage II Colorectal Cancer
    Trial name
    RESIST (NCT07829081)
    Testing
    Active surveillance after complete response to immunotherapy in MMRd GI cancers, Stand of Care
    Where
    3 sites in Switzerland
    Volunteers
    234 people
    Sponsor
    University Hospital, Basel, Switzerland
    Can I take part? RESIST

Completed, with results posted

All 6
  • Parkinson's Disease

    Evaluation of Intensive Language Therapy

    • Completed
    • Age: 45 to 80 years
    • Results posted

    Due to Parkinson's Disease (PD) speech and language (SL) deficits may occur. Further, the literature reports that PD patients, who have not undergone deep brain stimulation (DBS), have deficits regarding voice quality (e.g.

    Trial name
    EILT (NCT02935842)
    Testing
    Specific SL-therapy, Rhythmic Balance-Movement Training (rBMT)
    Where
    Switzerland
    Volunteers
    38 people, healthy volunteers welcome
    Sponsor
    University Hospital, Basel, Switzerland
    Can I take part? EILT
  • Emergency Service, Hospital, Information Structuring

    Basel Discharge Communication Project

    • Completed
    • Age: 18 years and older
    • Surgery or procedure
    • Results posted

    Assessing whether structuring of discharge information improves the sender's recall capacity

    Conditions
    Emergency Service, Hospital, Information Structuring, Physician-Patient Relations, Communication
    Trial name
    BACOP (NCT01540266)
    Testing
    Information structuring, no information structuring
    Where
    Switzerland
    Volunteers
    242 people, healthy volunteers welcome
    Sponsor
    University Hospital, Basel, Switzerland
    Can I take part? BACOP
  • Smoking Cessation, Alcohol Consumption

    Smoking Cessation in Alcoholics

    • Completed
    • Age: 18 to 65 years
    • Lifestyle or therapy programme
    • Results posted

    Most alcohol-dependent individuals are heavy smokers. The aim of this study is to evaluate whether a specific smoking cessation program (based on cognitive-behavioral therapy) for inpatient alcohol-dependent smokers is more…

    Trial name
    NCT00963482
    Testing
    Cognitive-behavioural smoking cessation program, Autogenic training
    Where
    Switzerland
    Volunteers
    103 people
    Sponsor
    University Hospital, Basel, Switzerland
    Can I take part? NCT00963482
  • Thromboembolism

    Self-management of Low Molecular Weight Heparin Therapy

    • Completed
    • Age: 18 years and older
    • Phase 4
    • Lifestyle or therapy programme
    • Results posted

    There is very little data available on compliance with self-injected low molecular weight heparins (LMWH), but what there is, definitely shows that compliance represents a significant problem.

    Trial name
    NCT00794560
    Testing
    patient education
    Where
    2 sites in Switzerland
    Volunteers
    154 people
    Sponsor
    University Hospital, Basel, Switzerland
    Can I take part? NCT00794560
  • Hyperglycemias

    Evaluation of an Algorithm for Intensive s.c. Insulin Therapy in Emergency Room Patients With Hyperglycaemia

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

    The aim of this study is to test the safety and efficacy of a new algorithm for intensive s.c. insulin injection in medical emergency patients with hyperglycaemia (plasma glucose concentration ≥ 8 mmol/l)

    Trial name
    NCT00353431
    Testing
    Novorapid ®, Novo Nordisk, Denmark
    Where
    Switzerland
    Volunteers
    130 people
    Sponsor
    University Hospital, Basel, Switzerland
    Can I take part? NCT00353431

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