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Research institution

Erasmus Medical Center Clinical Trials

Studies where Erasmus Medical Center is the lead sponsor: what is enrolling now, by phase, condition and country.

478 registered studies

In numbers

Open to volunteers
138
Active
166
With results posted
9
All registered
478

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

Open to volunteers

All 138
  • Peritoneal Metastases From Gastric Cancer

    INTERACT Stomach-II

    • Recruiting
    • Age: All ages
    • Phase 2

    This is a phase II study conducted in three hospitals in the Netherlands (Erasmus MC in Rotterdam, Catharina Hospital in Eindhoven, and the Netherlands Cancer Institute in Amsterdam). A total of 55 patients will take part.

    Trial name
    NCT07133490
    Testing
    intraperitoneal chemotherapy
    Where
    3 sites in Netherlands
    Volunteers
    55 people
    Sponsor
    Erasmus Medical Center
    Can I take part? NCT07133490
  • Trauma Associated Hemorrhage

    Prehospital Transfusion Outcomes in Traumatic Hemorrhage: a Prospective Cohort Study

    • Not yet recruiting
    • Age: 16 years and older
    • Observational study

    Traumatic injuries can cause severe bleeding, which causes a lot of deaths worldwide that could be prevented. Starting treatment as early as possible has been shown to improve survival, which makes fast care very important.

    Trial name
    PRONTO (NCT07883252)
    Where
    Netherlands
    Volunteers
    750 people
    Sponsor
    Erasmus Medical Center
    Can I take part? PRONTO
  • Aortic Valve Stenosis and/or Insufficiency, Hypoattenuated Leaflet Thickening

    SYMmetric Valve fraME Expansion To Reduce hYpoattenuated Leaflet Thickening After Balloon-expandable TAVI: the SYMMETRY Trial

    • Not yet recruiting
    • Age: 70 years and older
    • Surgery or procedure

    Rationale: Transcatheter aortic valve implantation (TAVI) has become the standard of care for aortic stenosis across all surgical risk categories, including low-risk, younger patients (≥70 years).

    Conditions
    Aortic Valve Stenosis and/or Insufficiency, Hypoattenuated Leaflet Thickening, Valve Expansion, Transcatheter Aortic Valve Replacement
    Trial name
    SYMMETRY (NCT07872020)
    Testing
    Double-TAP post-dilatation
    Where
    5 sites in Germany, Netherlands
    Volunteers
    422 people
    Sponsor
    Erasmus Medical Center
    Can I take part? SYMMETRY
  • Clinical Intuition

    CLINICAL INTUITION is an Experience-based, Often Unconscious Assessment of a Patient's Resilience and Tolerance. It is INFLUENCED by Clinical Signs, Behavior, Functioning, and Context. While it MAY PREDICT Patient Dropout, it is Difficult to Objectify.

    • Not yet recruiting
    • Age: All ages
    • Observational study

    Patient selection for Phase I oncology trials is formally based on protocol-defined inclusion and exclusion criteria. In practice, however, healthcare professionals also take clinical intuition and professional experience into…

    Trial name
    MINC (NCT07877623)
    Volunteers
    10 people, healthy volunteers welcome
    Sponsor
    Erasmus Medical Center
    Can I take part? MINC
  • Valve Heart Disease

    Balloon vs. Self Expanding Transcatheter Valve for Degenerated Bioprosthesis

    • Recruiting
    • Age: 18 years and older
    • Medical device

    Transcatheter aortic valve implantation (TAVI) serves a growing spectrum of patients with symptomatic severe aortic stenosis (AS). Approximately 80% of surgical aortic valve replacements are performed using a bioprosthesis.

    Trial name
    BASELINE (NCT04843072)
    Testing
    EVOLUT R/PRO/PRO+/FX bioprosthesis, Edwards Sapien S3/Ultra bioprosthesis, MYVAL/Octacor/Octapro bioprosthesis
    Where
    14 sites in United States, Austria and 10 more
    Volunteers
    600 people
    Sponsor
    Erasmus Medical Center
    Can I take part? BASELINE
  • Trauma Induced Coagulopathy, Trauma Coagulopathy

    Point of Care Fibrinogen Measurement in Trauma Patients in the Emergency Department

    • Recruiting
    • Age: 16 years and older
    • Observational study

    Background: Why This Study Matters When someone suffers a severe injury (like from a car crash), they can bleed heavily. One complication doctors often face is something called Trauma-Induced Coagulopathy (TIC).

    Conditions
    Trauma Induced Coagulopathy, Trauma Coagulopathy, Fibrinogen Deficiency, Fibrinogen; Deficiency, Acquired
    Trial name
    POCFIB (NCT07097337)
    Where
    Netherlands
    Volunteers
    50 people
    Sponsor
    Erasmus Medical Center
    Can I take part? POCFIB
  • Glioma, Glioblastoma (GBM)

    Pilot IntraOperative Neuronal Electrophysiology in Tumor rElatEd suRgery

    • Recruiting
    • Age: 18 years and older
    • Medical device

    INTRODUCTION AND RATIONALE Aggressive brain tumors like glioma have the ability to infiltrate the surrounding healthy brain tissue, disrupting normal neuronal activities and leading to impaired motor and cognitive functions, as…

    Conditions
    Glioma, Glioblastoma (GBM), Brain Tumor-Glioma, Brain Metastasis
    Trial name
    PIONEER (NCT06617208)
    Testing
    Neuropixel probe recording
    Where
    Netherlands
    Volunteers
    20 people
    Sponsor
    Erasmus Medical Center
    Can I take part? PIONEER
  • Rectal Cancer

    ctDNA-Based Adjuvant Chemotherapy for High-Risk Rectal Cancer

    • Recruiting
    • Age: 18 years and older
    • Phase 3

    The goal of this clinical trial is to investigate whether adjuvant chemotherapy can prevent disease recurrence in patients with high-risk rectal cancer who have detectable ctDNA after surgery.

    Trial name
    REACT (NCT07188025)
    Testing
    Adjuvant chemotherapy
    Where
    25 sites in Netherlands
    Volunteers
    103 people
    Sponsor
    Erasmus Medical Center
    Can I take part? REACT
  • Mesotheliomas Pleural

    dENdritic Cell Therapy Combined With SURgEry in Mesothelioma

    • Recruiting
    • Age: 18 years and older
    • Phase 1

    The ENSURE trial is an open label, single center, phase 1, feasibility study. Sixteen adult patients diagnosed with resectable epithelioid malignant pleural mesothelioma (MPM) will be enrolled following first-line chemotherapy.

    Trial name
    ENSURE (NCT05304208)
    Testing
    Mesopher
    Where
    Netherlands
    Volunteers
    16 people
    Sponsor
    Erasmus Medical Center
    Can I take part? ENSURE
  • Locally Advanced Cervical Cancer, Uterine Carcinoma

    Clinical Feasibility of the ARCHITECT Applicator in Cervical Cancer Brachytherapy

    • Recruiting
    • Age: 18 years and older
    • Medical device

    This prospective, non-randomised, single centre, phase I trial assesses the clinical feasibility of the use of the patient-tailored ARCHITECT applicator in locally advanced cervical cancer brachytherapy.

    Trial name
    ARCHITECT (NCT07435987)
    Testing
    ARCHITECT applicator
    Where
    Netherlands
    Volunteers
    25 people
    Sponsor
    Erasmus Medical Center
    Can I take part? ARCHITECT

Completed, with results posted

All 8
  • Atrial Fibrillation

    Effect of a Bigger Cryoballoon on the Total Antral Lesion Size: Evaluation of POLARx FIT

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

    The investigators will prospectively evaluate the extent of antral lesion created by the 31 mm balloon size of a novel cryoballoon catheter (POLARx FIT).

    Trial name
    BETTER-FIT (NCT05881733)
    Testing
    POLARx FIT cryoballoon
    Where
    Netherlands
    Volunteers
    20 people
    Sponsor
    Erasmus Medical Center
    Can I take part? BETTER-FIT
  • Anesthesia, Depth of Hypnosis Monitoring

    The Effect of DSA on Recovery of Anaesthesia in Children

    • Completed
    • Age: 6 months to 12 years
    • Medical device
    • Results posted

    In this randomised, blinded study, we will investigate the influence of DSA on recovery from general anaesthesia. DSA monitoring provides continuous information on depth of hypnosis.

    Trial name
    DSA-RCT-1 (NCT05525104)
    Testing
    Narcotrend Monitor (MT MonitorTechnik, Hannover, Germany)
    Where
    Netherlands
    Volunteers
    112 people
    Sponsor
    Erasmus Medical Center
    Can I take part? DSA-RCT-1
  • Aorto-Iliac Arterial Stenosis, Peripheral Arterial Disease

    Aortoiliac Stenosis in Kidney Transplantation

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

    The impact of aortoiliac stenosis on kidney transplant patients remains unclear. This study aims to investigate the safety and efficacy of kidney transplantation in patients with aortoiliac stenosis.

    Conditions
    Aorto-Iliac Arterial Stenosis, Peripheral Arterial Disease, Kidney Transplant Failure
    Trial name
    TASC (NCT06020534)
    Where
    Netherlands
    Volunteers
    655 people
    Sponsor
    Erasmus Medical Center
    Can I take part? TASC
  • Anxiety

    Resistance Under the Microscope

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

    The purpose of this study is to determine whether lorazepam, which is used to lower preoperative anxiety, also improves postoperative recovery.

    Trial name
    NCT01441843
    Testing
    Lorazepam, NaCl 0.9% (Sodium Chloride)
    Where
    Netherlands
    Volunteers
    400 people
    Sponsor
    Erasmus Medical Center
    Can I take part? NCT01441843
  • Inflammatory Bowel Diseases

    Biomarkers of Anti-TNF Treatment in Inflammatory Bowel Disease (IBD)

    • Completed
    • Age: 6 years and older
    • Observational study
    • Results posted

    Anti-TNF treatment (infliximab (IFX), adalimumab (ADA)) has become standard therapy for refractory pediatric and adult Crohn's disease (CD) patients, and is used for the induction (primary response) and maintenance of remission.

    Trial name
    NCT01971970
    Testing
    Infliximab, Adalimumab
    Where
    Netherlands
    Volunteers
    45 people
    Sponsor
    Erasmus Medical Center
    Can I take part? NCT01971970

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