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All Clinical Trials in United Kingdom
A listing of 3097 clinical trials actively recruiting volunteers for paid trials and research studies in various therapeutic areas.
2125 - 2136 of 3097
Fosfomycin I.v. for Treatment of Severely Infected Patients
Recruiting
The purpose of this European, multicentric, prospective, non-interventional study is to document and evaluate the efficacy and safety of the treatment of severely infected patients with intravenously administered fosfomycin, including patients with osteomyelitis, complicated urinary tract infection, nosocomial lower respiratory tract infection, bacterial meningitis/central nervous system infection, bacteraemia/sepsis, skin and soft tissue infection, endocarditis or other infections, each as far... Read More
Gender:
ALL
Ages:
18 years and above
Trial Updated:
09/27/2024
Locations: Landeskrankenhaus Hall - Tirol Kliniken, Hall In Tirol, Not set +49 locations
Conditions: Bacterial Infections, Bone Diseases, Infectious, Osteomyelitis, Central Nervous System Bacterial Infections, Meningitis, Bacterial, Encephalitis, Brain Abscess, Urinary Tract Infections, Respiratory Tract Infections, Pneumonia, Bacterial, Skin Diseases, Bacterial, Soft Tissue Infections, Intraabdominal Infections, Sepsis, Bacteremia, Endocarditis, Bacterial
Cognitive Muscular Therapy for People Awaiting Knee Joint Replacement
Recruiting
The primary aim will seek to understand whether Cognitive Muscular Therapy (CMT) could provide pain relief for people on a waiting list for joint replacement.
Gender:
ALL
Ages:
40 years and above
Trial Updated:
09/26/2024
Locations: University of Salford, Manchester, Greater Manchester
Conditions: Knee Osteoarthritis
Study BT8009-100 in Subjects With Nectin-4 Expressing Advanced Malignancies
Recruiting
This study is a Phase I/II, multicenter, first-in-human, open-label dose-escalation study of BT8009 given as a single agent and in combination with pembrolizumab in participants with advanced solid tumors associated with Nectin-4 expression or in participants with advanced solid tumor malignancies having renal insufficiency. The primary endpoints are: Dose limiting toxicities (Parts A-1 and A-2), Overall response rate per RECIST v1.1 (Parts B1-B7), Safety and tolerability (Parts B-8, B-9 and C),... Read More
Gender:
ALL
Ages:
18 years and above
Trial Updated:
09/26/2024
Locations: Sarah Cannon Research Institute at HealthONE, Denver, Colorado +28 locations
Conditions: Advanced Solid Tumor, Urinary Bladder Neoplasm, Triple Negative Breast Neoplasms, Ovarian Neoplasm, Hormone Receptor Positive, HER2-negative Neoplasms, Hormone Receptor Positive, HER2-low Neoplasms, Breast Neoplasms, Non-Small-Cell Lung Neoplasms
Olorofim Aspergillus Infection Study
Recruiting
The purpose of this study is to compare treatment with olorofim versus treatment with AmBisome® followed by standard of care (SOC) in patients with IFD caused by proven IA or probable lower respiratory tract disease Aspergillus species (invasive aspergillosis, IA).
Gender:
ALL
Ages:
18 years and above
Trial Updated:
09/26/2024
Locations: University of Alabama at Birmingham, Birmingham, Alabama +139 locations
Conditions: Invasive Aspergillosis
Low Energy Availability and Cardiovascular Disease
Recruiting
Low energy availability (LEA) signifies a condition where the body lacks sufficient energy to support essential physiological functions crucial for maintaining optimal health (1). This energy insufficiency can be exacerbated by the demands of sports and exercise, resulting in negative impacts on various physiological, psychological, and sports performance (11, 8, 2). While LEA is commonly associated with cardiovascular abnormalities, such as early atherosclerosis, endothelial dysfunction, and lo... Read More
Gender:
FEMALE
Ages:
Between 18 years and 35 years
Trial Updated:
09/24/2024
Locations: Liverpool Hope University, Liverpool, Merseyside
Conditions: Low Energy Availability, Cardiovascular Diseases
Optimising Pacing for Contractility 2
Recruiting
The investigators have demonstrated that they can reliably identify an optimum heart rate range for contractility of the left ventricle in patients with chronic heart failure (CHF). They have also demonstrated in an acute cross-over and a small parallel group feasibility study that keeping the heart rate in this range (versus standard rate-response programming) in patients with CHF is associated with increased exercise time on a treadmill (around 60s or 10%). They now want to explore in a random... Read More
Gender:
ALL
Ages:
18 years and above
Trial Updated:
09/24/2024
Locations: Leeds General Infirmary, Leeds, Not set
Conditions: Heart Failure, Systolic, Pacemaker
Predicting the Risk of Non-culprit Coronary Artery Disease After a Heart Attack
Recruiting
Heart attacks caused by the complete blockage of a heart artery are treated by opening it with a stent. However, most people will also have 'non-culprit' narrowings found in their other arteries at this time.
Although in general people do better if these non-culprit narrowings are also treated with stents if they look severe, this process has problems. This is because narrowings that look severe may be stable and not cause any trouble. For these people a stent is a wasted procedure and unnecess... Read More
Gender:
ALL
Ages:
18 years and above
Trial Updated:
09/24/2024
Locations: St Thomas' Hospital, London, Not set +1 locations
Conditions: Coronary Artery Disease, ST Elevation Myocardial Infarction, Ischemic Heart Disease
A Study of Radspherin® in Patients with Primary Advanced Epithelial Cancer, with Peritoneal Metastasis That Are Homologous Recombination Proficient Scheduled to Undergo Neoadjuvant Chemotherapy and Interval Debulking Surgery
Recruiting
This is a Phase 2, controlled, randomised, parallel assignment, open label, multicentre study to evaluate efficacy and safety of a single intraperitoneal injection of Radspherin® in patients with primary advanced high-grade serous or high-grade endometrioid epithelial ovarian cancer, fallopian tube, or primary peritoneal cancer, with peritoneal metastasis that are HR proficient and scheduled to undergo NACT and IDS. The study will be conducted in 2 parts; first, a Safety Lead-in Cohort will be r... Read More
Gender:
FEMALE
Ages:
18 years and above
Trial Updated:
09/24/2024
Locations: Moffitt Cancer Center, Tampa, Florida +5 locations
Conditions: Peritoneal Carcinomatosis, Ovarian Cancer
Impact of Tixel Treatment on Symptoms and Signs in Patients with Dry Eye Disease
Recruiting
This study will examine how a standard Tixel treatment versus a sham treatment for eye wrinkles affects the symptoms and signs of Dry Eye Disease.
Gender:
ALL
Ages:
18 years and above
Trial Updated:
09/24/2024
Locations: Vision Science, School of Optometry, Birmingham, Not set
Conditions: Dry Eye Disease (DED)
Remote Ischaemic Conditioning (RIC) in Heart Failure
Recruiting
This study will test the impact of remote ischaemic conditioning combined with exercise on myocardial perfusion in patients with or at risk of heart failure
Gender:
ALL
Ages:
18 years and above
Trial Updated:
09/23/2024
Locations: Glenfield Hospital, Leicester, Leics
Conditions: Heart Failure With Preserved Ejection Fraction, Type 2 Diabetes, Dilated Cardiomyopathy
Characterisation of Endothelial Cells in Different Inflammatory Pathologies
Recruiting
The goal of this observational study is to characterise changes in gene expression in endothelial cells in patients with either sepsis or post major abdominal surgery.
The main question we plan to answer is: 'What molecular pathways are differentially expressed during inflammatory pathologies?'
Gender:
ALL
Ages:
18 years and above
Trial Updated:
09/23/2024
Locations: Royal Surrey NHS Foundation Trust, Guildford, Surrey
Conditions: Sepsis, Vasoplegia
A Multicentre Observational Study to Assess Long-term Outcome of Participants in the EXCELLENT Clinical Trial
Recruiting
The PERFECT study is an observational study designed to follow patients randomised in the EXCELLENT study (NCT02669810) for 10 years.
The aim is to assess the long-term clinical outcomes for patients randomised to the Standard of Care arm or the ProtheraCytes arm.
Gender:
ALL
Ages:
18 years and above
Trial Updated:
09/23/2024
Locations: CHU DIJON Hôpital François Mitterrand 14 rue Gaffarel, Dijon, Not set +9 locations
Conditions: Acute Myocardial Infarction
2125 - 2136 of 3097
