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Research institution

Queen Mary University of London Clinical Trials

Studies where Queen Mary University of London is the lead sponsor: what is enrolling now, by phase, condition and country.

253 registered studies

In numbers

Open to volunteers
58
Active
73
With results posted
15
All registered
253

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

Open to volunteers

All 58
  • Tendinopathy, Musculoskeletal Diseases or Conditions

    Human Tendon Tissue Collection

    • Not yet recruiting
    • Age: 18 years and older
    • Observational study

    The goal of this study is to improve understanding of tendon health and disease by using surplus tendon tissue that is routinely removed during planned orthopaedic surgeries in adults.

    Conditions
    Tendinopathy, Musculoskeletal Diseases or Conditions, ACL Surgery, Achilles Tendon Surgery
    Trial name
    NCT07606092
    Where
    2 sites in United Kingdom
    Volunteers
    400 people
    Sponsor
    Queen Mary University of London
  • Coronary Artery Disease (CAD), Stable Angina Pectoris

    Identification of Lesion Characteristics in Coronary Plaques Using Multimodality Intravascular Imaging and Novel Photon-counting CT in Stable Angina

    • Recruiting
    • Age: 18 to 79 years
    • Observational study

    Coronary artery disease, caused by the furring up of the heart arteries by atherosclerosis, is a major cause of death in the UK.

    Conditions
    Coronary Artery Disease (CAD), Stable Angina Pectoris, Ischaemic Heart Disease (IHD)
    Trial name
    ILUMINA (NCT07864025)
    Testing
    observational study
    Where
    United Kingdom
    Volunteers
    70 people
    Sponsor
    Queen Mary University of London
    Can I take part? ILUMINA
  • Coronary Artery Disease (CAD)

    Predicting Plaque Growth Using Blood Flow Stress Markers: A Proof-of-Concept Study

    • Recruiting
    • Age: 40 years and older
    • Surgery or procedure

    Coronary artery disease occurs when fatty deposits (plaques) build up inside the arteries that supply blood to the heart. Some plaques remain stable, while others continue to grow or become more likely to rupture, which can lead…

    Trial name
    POSSEM (NCT07864051)
    Testing
    PCCTA scan, Endothelial cell isolation from peripheral blood sample
    Where
    United Kingdom
    Volunteers
    270 people
    Sponsor
    Queen Mary University of London
    Can I take part? POSSEM
  • Myocardial Infarction, Stable Angina

    Barts Revascularisation Registry

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

    Despite the year-on-year decrease, coronary artery disease (CAD) still remains one of the leading cause of mortality worldwide. With advances in technology and our understanding of cardiac disease, we can now treat CAD using…

    Trial name
    NCT05255705
    Testing
    Observation only
    Where
    United Kingdom
    Volunteers
    20,000 people
    Sponsor
    Queen Mary University of London
  • Parkinson Disease (PD), REM Sleep Behavior Disorder (iRBD)

    Artificial Intelligence-based Parkinson's Disease Risk Assessment (AI-PRA) Study

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

    The study aims to provide initial proof-of-concept validation data of an artificial intelligence-based model to estimate individual Parkinson's disease risk using demographic, clinical, genetic information and digital biomarker…

    Conditions
    Parkinson Disease (PD), REM Sleep Behavior Disorder (iRBD), Neurogenic Orthostatic Hypotension, Hyposmia
    Trial name
    AI-PRA (NCT07706829)
    Testing
    Smartwatch and phone app
    Where
    3 sites in France, Spain and 1 more
    Volunteers
    60 people
    Sponsor
    Queen Mary University of London
    Can I take part? AI-PRA
  • Guided Bone Regeneration, Bone Resorption

    The Effect of IPD on Lateral Bone Augmentation

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

    Guided Bone Regeneration (GBR) is a widely used technique during dental implant surgery to help rebuild bone around the implant and improve its long-term appearance and stability.

    Conditions
    Guided Bone Regeneration, Bone Resorption, Diagnostic Imaging
    Trial name
    NCT06999915
    Testing
    Group 1 (Test Group): IP and GBR as an over-contour augmentation beyond IPD, Group 2 (Control Group): IP and GBR as a contour augmentation up to IPD
    Where
    United Kingdom
    Volunteers
    28 people
    Sponsor
    Queen Mary University of London
    Can I take part? NCT06999915
  • Hip Fractures, Venous Thromboembolism (VTE)

    Delivery and Implementation of a Randomised Crossover Trial on Thrombosis

    • Recruiting
    • Age: 60 to 120 years

    What is the Study About? The DIRECT study (Delivery and Implementation of a Randomised Crossover Trial on Thrombosis) is a large research project investigating the best way to prevent blood clots (thrombosis) in people who break…

    Trial name
    DIRECT (NCT06937372)
    Testing
    Patients in hospitals allocated to this arm will receive aspirin as their routine thromboprophylaxis after surgery., Low molecular weight heparin (LMWH)
    Where
    United Kingdom
    Volunteers
    21,194 people
    Sponsor
    Queen Mary University of London
    Can I take part? DIRECT
  • Coronary Artery Disease, Myocardial Infarction

    Barts Sex-CAD Database - Sex Hormones and Inflammatory Status in Coronary Artery Disease

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

    There is a lack of understanding of how Coronary Artery Disease (CAD) - meaning the blocking or furring up of the arteries of the heart - starts and progresses in women.

    Conditions
    Coronary Artery Disease, Myocardial Infarction, Acute Coronary Syndrome, Atherosclerosis
    Trial name
    NCT06327984
    Where
    United Kingdom
    Volunteers
    6,000 people
    Sponsor
    Queen Mary University of London
  • Primary Aldosteronism, High Blood Pressure

    Diagnosing Variable Primary Aldosteronism.

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

    The goal of this observational study is to see if there is a cyclical or exaggerated diurnal variation in aldosterone production in people with Primary Aldosteronism.

    Trial name
    NCT05765786
    Where
    United Kingdom
    Volunteers
    100 people
    Sponsor
    Queen Mary University of London
  • Relapsing Remitting Multiple Sclerosis, Primary Progressive Multiple Sclerosis

    SIZOMUS Safety of Ixazomib Targeting Plasma Cells in Multiple Sclerosis

    • Recruiting
    • Age: 18 to 65 years
    • Phase 1

    The study seeks to investigate safety and efficacy of ixazomib (NINLARO), a proteasome inhibitor, in multiple sclerosis (MS). Participants will receive either ixazomib capsules or placebo capsules for up to 24 months.

    Conditions
    Relapsing Remitting Multiple Sclerosis, Primary Progressive Multiple Sclerosis, Secondary Progressive Multiple Sclerosis
    Trial name
    SIZOMUS (NCT03783416)
    Where
    United Kingdom
    Volunteers
    72 people
    Sponsor
    Queen Mary University of London
    Can I take part? SIZOMUS

Completed, with results posted

All 14
  • Multiple Sclerosis

    Oral Cladribine B-cell Study

    • Completed
    • Age: All ages
    • Observational study
    • Results posted

    To study the impact of cladribine on peripheral and intrathecal B-cell, plasma cells, T cells and Tregs

    Trial name
    NCT06415864
    Where
    United Kingdom
    Volunteers
    10 people
    Sponsor
    Queen Mary University of London
    Can I take part? NCT06415864
  • Ischemic Stroke, Thrombotic Stroke

    Autonomic Neuromodulation by Transcutaneous Nerve Stimulation in Acute Ischaemic Stroke.

    • Completed
    • Age: 18 to 95 years
    • Medical device
    • Results posted

    Autonomic modulation by transcutaneous vagal nerve stimulation in acute ischaemic stroke requiring mechanical thrombectomy: a phase IIa, sham controlled randomised trial.

    Conditions
    Ischemic Stroke, Thrombotic Stroke, Autonomic Dysfunction, Autonomic Imbalance
    Trial name
    VANS (NCT05417009)
    Testing
    trans-cutaneous auricular sensory stimulation
    Where
    United Kingdom
    Volunteers
    36 people
    Sponsor
    Queen Mary University of London
    Can I take part? VANS
  • Healthy Volunteers

    SPM Regulation by Fish Oil Supplements in Healthy Volunteers

    • Completed
    • Age: 18 to 45 years
    • Results posted

    A randomised, double-blind, placebo-controlled study to determine whether fish oil supplementation regulates peripheral levels of specialized pro-resolving mediators and white blood cell responses in healthy volunteers

    Trial name
    NCT03347006
    Testing
    SPM Active
    Where
    United Kingdom
    Volunteers
    22 people, healthy volunteers welcome
    Sponsor
    Queen Mary University of London
    Can I take part? NCT03347006
  • Retention, Compliance

    Evaluation of Tailored Electronic Reminders on Compliance With Removable Orthodontic Retention

    • Completed
    • Age: 12 to 21 years
    • Results posted

    Participants will be recruited for inclusion at a routine adjustment appointment prior to planned removal of the appliances. Following removal of the appliances, consenting participants will be randomly allocated to one of two…

    Conditions
    Retention, Compliance, Orthodontic, Periodontal Health
    Trial name
    NCT03224481
    Testing
    Electronic reminder
    Where
    United Kingdom
    Volunteers
    84 people, healthy volunteers welcome
    Sponsor
    Queen Mary University of London
    Can I take part? NCT03224481
  • Dyssynergic Defaecation, Evacuation Disorder

    Infracoccygeal Botox for Dyssynergia

    • Completed
    • Age: 18 to 80 years
    • Observational study
    • Injection or infusion
    • Surgery or procedure
    • Results posted

    Background: Constipation is a common problem, affecting up to 20% of the population during their lifetime. Some patients respond poorly to standard treatments such as laxatives.

    Conditions
    Dyssynergic Defaecation, Evacuation Disorder, Anismus, Defecation Disorder
    Trial name
    NCT04879524
    Testing
    Percutaneous infracoccygeal Botulinum toxin injection to puborectalis
    Where
    United Kingdom
    Volunteers
    8 people
    Sponsor
    Queen Mary University of London
    Can I take part? NCT04879524

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