Clinical trials

9

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Thrombectomy in Pulmonary Embolism

Pulmonary embolism is a blood clot on the lung, which can cause death or significant reduced quality of life. Sucking the clot out with a special tube (catheter) is a relatively new procedure that can be performed but doesn't have the data required to properly support its use in some patients. We know this procedure works in patients who have no other options and would almost certainly die without intervention. We currently don't know how well this procedure is tolerated, how well it works and what its complications are in patients who are moderately to severely unwell. The National Institute of Clinical Excellence (NICE), an advisory body, suggests more data is required to support its use in patients who are sick or very sick. This registry aims to support this growing evidence base to workout if the treatment is effective and the associated risks that come with using it. We are collecting data about this procedure and other treatments patients get offered to better inform clinicians and researchers.

Participants needed: 2,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University Hospital Plymouth NHS TrustUpdated: Jun 25, 2026Locations: 1
Eligibility criteria

Clinical signs and symptoms consistent with acute pulmonary embolism with durati... [+6]

Known serious, uncontrolled sensitivity to radiographic agents [+12]

Status: Not yet recruiting

5 Minute 'HOT' Trauma CT Rates Of Detection Study

Many injured patients receive urgent CT imaging to identify major injury. CT imaging of trauma patients is often time critical and the accurate detection of life-threatening findings on this CT is essential. Often following a scan a radiologist is not immediately available to review the imaging, however other members of the trauma team have access to the imaging and may be in a position to provide a "hot" report. In this study we aim to demonstrate if an educational intervention with a checklist improves accuracy of the hot report.

Participants needed: 300
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital Plymouth NHS TrustUpdated: Jan 12, 2026Locations: 1
Eligibility criteria

Medical professionals involved in trauma image review. [+2]

Unable to review CT imaging due to lack of previous experience or disability tha... [+2]

Status: Not yet recruiting

Opinions, Perceptions, & Thoughts of British Resident Doctors on Orthopaedics

Orthopaedic surgery is one of the largest surgical specialties in the UK, delivering high-volume, high-impact care across trauma and elective pathways. Despite this, the specialty continues to face challenges in recruitment, diversity, inclusivity and perceptions of workload and culture. International literature suggests that impressions formed during undergraduate and early postgraduate training strongly influence specialty choice; however, contemporary UK-specific data on how resident doctors view orthopaedics remain limited. The ORTHO BRO Study is a cross-sectional, anonymous online survey designed to capture UK trainees' perceptions of orthopaedics, compare views between those with and without prior orthopaedic rotations, and explore spontaneous associations. Findings will inform training improvement, inclusivity initiatives, and recruitment strategies. The study targets UK foundation doctors (F1/F2), core trainees (CT1/CT2), and trust-grade/non-training senior house officers (SHOs) across multiple trusts/foundation schools.

Participants needed: 300
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University Hospital Plymouth NHS TrustUpdated: Dec 15, 2025
Eligibility criteria

Are currently employed within the UK National Health Service (NHS) as a Foundati... [+4]

Status: Recruiting

Splenic Embolisation Decisions

The spleen is often injured when the body sustains trauma. This leads to bleeding. The bleeding can be stopped by a big operation cutting open the belly or a small hole in your groin where a blood vessel can be accessed and through which the bleeding can be stopped. We do not know what types of injuries it is best to use this procedure. We do not know why we do not use the smaller technique in some instances. We also do not know exactly which of a number of ways to stop the bleeding could be better. We have a big data set in the trauma and audit research network (TARN) which we would like to use to help answer these questions and design further studies to better answer the questions. Adding a few other pieces of data, we are able to answer key questions into how the spleen will best be treated in trauma.

Participants needed: 8,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University Hospital Plymouth NHS TrustUpdated: Dec 4, 2025Locations: 1Duration: 3 Years
Eligibility criteria

Not listed

Status: Not yet recruiting

Quality of Life Improvement After TAVI (QualiTAVI-UK Trial)

Transcatheter aortic valve implantation (TAVI) has become an important therapeutic intervention for patients with symptomatic severe aortic stenosis (AS) who are at high surgical risk. While the clinical outcomes of TAVI are well established, there is limited data on the long-term quality of life (QoL) following the procedure. This prospective study will assess QoL in patients undergoing TAVI at Derriford Hospital, University Hospitals Plymouth, UK. Investigators will employ the Kansas City Cardiomyopathy Questionnaire (KCCQ-12) and Mini-Montreal Cognitive Assessment (Mini-MoCA) to evaluate both physical and mental health outcomes, supplemented by an analysis of life expectancy estimated by a multidisciplinary team (MDT). Data will be collected at referral, pre-procedural, 30 days, and 3 months post-TAVI. This will be the first prospective trial focused on QoL improvement after TAVI, as all previous studies have been retrospective in nature. The study aims to provide comprehensive insights into the QoL improvements after TAVI, which will guide future clinical decision-making in this population.

Participants needed: 100
Trial details
Biological sex: AllType: ObservationalSponsor: University Hospital Plymouth NHS TrustUpdated: Sep 30, 2025Locations: 1Duration: 3 Months
Eligibility criteria

Patients who were eligible and accepted for TAVI procedure regardless of the pat...

Patients who declined enrollment in this research.

Status: Recruiting

Tolerance in Beekeepers

Beekeepers experience multiple bee stings each year. Many of these beekeepers (25-60%) become sensitized to bee venom through the production of specific antibodies that target the bee venom. Although these antibodies are important in the triggering of an allergic reaction only a small number of sensitised beekeepers go on to have an allergic reaction with symptoms away from the site of the sting. These reactions can be severe and are known as anaphylactic reactions. The study investigates why some beekeepers develop severe allergic symptoms after bee stings while others do not. This study will explore factors in the blood that protect sensitised individuals from having anaphylactic reactions - meaning that despite being sensitised they are tolerant and do not react to subsequent stings.

Participants needed: 120
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University Hospital Plymouth NHS TrustUpdated: Apr 30, 2025Locations: 1
Eligibility criteria

Individuals naive to beekeeping (<2 previous bee stings, none in the last 24 mon... [+4]

Unable to understand protocol/consent. [+4]

Status: Not yet recruiting

Ergonomic Challenges for Surgeons; The Problem and Solutions

Work-related musculoskeletal disorders (WMSDs) are highly prevalent among surgeons. Despite growing awareness, there remains a lack of detailed data on the specific postures that contribute to ergonomic risk, particularly within General Surgery. This study aims to characterise postures encountered during open, laparoscopic, and robotic gastrointestinal procedures using wearable sensor technology and video analysis, to inform future ergonomic interventions and training. A single-centre, prospective observational study of 30 surgical cases will be conducted at University Hospitals Plymouth NHS Trust. Participating surgeons will wear inertial measurement units (IMUs) to record real-time body segment position data whilst performing live surgery. A biomechanical model will then be used to calculate joint angles and whole body posture. Video recordings will be synchronised with IMU data to map posture to surgical tasks. Static and dynamic postures will be analysed using standard ergonomic assessment tools. Alternative tools tailored to surgery will be assessed and proposed. Surgeons will complete questionnaires pre- and post-operatively to report musculoskeletal symptoms. Outcomes will compare ergonomic risk across surgical techniques, identify high-risk procedural steps, and assess the acceptability of wearable technologies in the operating theatre. The data generated will also be used to evaluate, train or refine artificially intelligent camera-based pose estimation models for the operating theatre environment in order to make future ergonomics research and assessment more accessible.

Participants needed: 30
Trial details
Biological sex: AllType: ObservationalSponsor: University Hospital Plymouth NHS TrustUpdated: Apr 22, 2025Locations: 1
Eligibility criteria

Surgeons performing gastro-intestinal (GI) surgery [+4]

Pre-existing severe practice-limiting musculoskeletal disorder [+2]

Status: Not yet recruiting

Evaluation of the Eyhance and Zoe Lenses

The goal of this observational study is to assess distance and near visual acuity of patients who have undergone cataract surgery with two intraocular lenses (IOLs). The main outcomes are: To assess distance and near visual acuity of patients who have undergone cataract surgery with two intraocular lenses (IOLs) To assess depth of focus of the IOLs To assess tilt and decentration of the IOLs The potential participants will be chosen from the list of patients in the Southend NHS database who have had routine cataract surgery using the Zoe or Eyhance lenses in the past 12 months and contacted by phone and letter. The member of the ophthalmological team carrying out the screening will use the research inclusion and exclusion criteria to identify 50 potential participants. Once identified, the potential participants will be asked if they would be willing to discuss inclusion into the study with a member of the clinical care team (Prof Myerscough or Dr Law). If they agree, they will be asked to attend one further clinical visit. They will be given a patient information sheet and consent form at this visit. All potential participants will be informed that participation in this research study will be entirely voluntary. At the clinical visit participants will have their vision assessed, have dilating drops instilled, and undergo two non-invasive scans of their eyes.

Participants needed: 50
Trial details
Age: 18-90Biological sex: AllType: ObservationalSponsor: University Hospital Plymouth NHS TrustUpdated: Oct 30, 2024
Eligibility criteria

Adult (over 18) patients with cataract requiring cataract surgery with phacoemul... [+1]

Previous penetrating keratoplasty or anterior lamellar keratoplasty [+2]

Status: Not yet recruiting

Generational Diversity in the Medical Profession

The purpose of this work is to investigate how post-graduate doctors in training (PGDiTs) experience generational diversity with their colleagues in the workplace. The investigators want to explore and understand how PGDiTs perceive and experience generational diversity in the workplace and look into where these differences between generations could come from. The research team wants to do this by running focus groups. These focus groups would be made up of PGDiTs that are working within one hospital. The doctors will be split into the different generations (i.e. generation X, Y and Z). A set list of questions will be used to prompt and guide the focus group conversations. Each focus group will be audio-recorded using an electronic device and then analysed with the aid of computer software. The investigators will then generate themes from the data and use this to create an overall story of the data. It is hoped that this research can help inform supervisors and employers of the impact of generational diversity on on PGDiTs. This may be used to help develop ways of improving working relationships for PGDiTs with their supervisors and employers.

Participants needed: 30
Trial details
Age: 18-100Biological sex: AllType: ObservationalSponsor: University Hospital Plymouth NHS TrustUpdated: Jun 21, 2024
Eligibility criteria

Any medically qualified healthcare professional with a General Medical Council (... [+7]