Read our FAQs here
Safe, expert care from our specialist clinical trial medical and support team, with on-site appointments delivered face to face at our dedicated clinical research sites. Ongoing support is available whenever you need it throughout your time taking part on a research study.
The Bodyline Birkenhead clinical trial site offers a welcoming and supportive environment for individuals taking part in clinical research. All studies are conducted in line with consistent standards, ensuring participant safety, clear communication, and a well-supported experience throughout.
Conveniently located for participants in Birkenhead and across the Wirral, Merseyside, and North Wales regions, the site is easily accessible via Chester Street (A41), with strong transport links to the M53, Queensway Tunnel, and major routes into Liverpool, Chester, and the A55 corridor.
124 Chester Street, Birkenhead, Liverpool, CH41 5DL
Visit by appointment only.
Call 0800 995 6036 for further information.
clinicaltrials@bodylineclinic.com
What to expect at Your Clinical Trial Appointment
Our team provides specialist clinical trial care from experienced medical experts and wider clinical trial support team. Bodyline are with you at every stage of your clinical trial participation. All of our clinics are CQC accredited, ensuring high standards of safety, quality, and care.
Our Trustpilot Reviews
A clinical trial at Bodyline is a carefully designed research study conducted on behalf of pharmaceutical companies and clinical research partners. These studies evaluate new treatments, medications, or approaches to managing obesity, weight, metabolic health and related therapeutic areas, following strict regulatory and ethical standards.
Bodyline works in partnership with pharmaceutical sponsors, contract research organisations (CROs) and other clinical trial site networks to deliver high-quality clinical trials. We provide experienced clinical sites, access to suitable participants, and consistent study delivery in line with sponsor protocols.
We specialise in obesity, weight management, metabolic health, and female health studies, including trials for emerging therapies and real-world evidence generation.
Clinical trials are essential for developing and approving new treatments. By working with research partners, Bodyline helps generate reliable data to support emerging therapies and bring innovative treatments closer to real-world clinical use.
Each study has specific eligibility criteria set by the sponsor, which may include factors such as age, BMI, and medical history. Our team will carry out a simple and confidential pre-screening process to determine suitability.
You can register your interest by completing our online enquiry form or contacting our team directly. We will then match you to any suitable ongoing or upcoming studies.
At your initial visit, our research team will explain the study, including its purpose, duration, and any potential risks or benefits. You'll have time to ask questions before providing informed consent, and baseline assessments may be carried out if appropriate.
You'll receive specialist clinical trial care from Bodyline's experienced team, who deliver studies on behalf of sponsors while ensuring a patient-centred experience. We provide clear guidance, regular follow-ups, and ongoing monitoring throughout your participation.
Yes. All trials delivered by Bodyline are conducted in line with strict UK regulatory and ethical guidelines, as well as sponsor protocols, with participant safety as the highest priority.
No. Participation is free. Some studies may also offer reimbursement for reasonable travel expenses, depending on the sponsor.
Depending on the study design set by the sponsor, you may receive the investigational treatment, standard care, or a placebo. This will always be clearly explained before you decide to take part.
A placebo is a substance with no active treatment effect, used in some studies for comparison. Not all trials include a placebo, and this will be clearly explained to you in advance.
Study duration is defined by the sponsor and varies depending on the trial. Some may last a few weeks, while others may run for several months.
Visit schedules vary by study but are clearly outlined before you enrol. Some trials may include a combination of in-clinic visits and remote follow-ups where appropriate.
Yes. Participation is entirely voluntary, and you can withdraw at any time without affecting your standard care.
You may gain access to new treatments under development, receive regular clinical monitoring, and contribute to research that supports future patient care and treatment innovation.
As with any medical research, there may be potential risks or side effects. These will be fully explained before you agree to take part, and you will be closely monitored throughout the study.
Yes. Your data is handled securely in compliance with data protection regulations and sponsor requirements, ensuring full confidentiality at all times.
At the end of the study, you will be informed of next steps, which may include follow-up care or guidance. In some cases, participants may be offered continued access to treatment, depending on the study design.
