Recruiting Adults With Dyslipidemia

You may receive up to £900
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Summary

  • We are conducting a patient engagement for participants with dyslipidemia (high or low levels of fats in the blood).
  • In this study, we are recruiting men and women between the ages of 18 and 72.
  • We will give you a tour of the clinical trials unit and conduct several clinical assessments to establish your current health status. This study is to help participants with dyslipidemia decide if they want to participate in future gene editing clinical trials.
  • You will be reimbursed for your time and effort in this study.

If you are interested in participating in this patient engagement study:

  • You will need to attend an in-person appointment (Day 1) so we can check if you are eligible to take part in this patient engagement study. At this appointment, we will perform several tests such as taking blood, checking your heart, and conducting a physical examination. You will also be given a tour of the clinical trials unit and can ask the study staff any questions you may have. This may be done over more than 1 day if needed.
  • There will then be a follow-up phone call with a Study Doctor scheduled a week after Day 1 on Day 7 to discuss the results of the clinical investigations you have undergone and provide you with the opportunity to ask any questions.
  • You will then have follow-up calls every 12 weeks with the Study Doctor and if there are any significant changes in your health, they may ask you to come in for an optional in-person visit.
  • This study does not require you to take any investigational medication.

Who can take part?

We will check your eligibility for the Patient Engagement study using the following criteria:

  • You must be a male or female aged 18 to 72 years.
  • You must have a history of dyslipidaemia and ASCVD (Atherosclerotic cardiovascular disease) and are considering participation in future clinical trials.
  • You must be willing to comply with study procedures and assessments, including follow-up visits.

Duration of Stay

You will need to attend an in-person appointment (Day 1), and a follow-up phone call every 12 weeks with the Study Doctor.

Patient engagement study reimbursement

In recognition of the time and effort involved in taking part in the study, you may receive up to £900 on completion of the study, provided you comply fully with all the study requirements.

Location

We are based in London Bridge near both the Underground and overhead train Stations.
Our unit address is:   Richmond Pharmacology 1A Newcomen Street (Corner of Newcomen and Borough High Street) London SE1 1YR Please note the postcode will take you 5 minutes down the road from the clinic, I would use the map below as a reference (the clinic is on Borough High St, just up from Tesco and opposite the road from Foxtons)

Dates

Please call a recruitment team member on 02070425800 to discuss study dates, or register to receive a call back.

Approval

The contents of this email have been approved by an ethics committee. Any response to this advertisement will be recorded. Your response will not place you under any obligation to participate in this study.

Ref: C24010_Jan-2025 (email_website_advert text)

Trial code:
C24010

Speak to a member of our Volunteer Recruitment Team

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Call: 020 7042 5800

Comments from volunteers

Thanks very much to the Volunteer Recruitment Team. I am so excited to be part of this trial. I can’t thank you and your colleagues enough for all your help, professionalism, and kindness.

Steve K

Unbelievable service! They looked after me so well, and I would recommend them to anyone interested in participating in a clinical trial. I want to thank all the staff at trials4us for their continued efforts and for looking after me so well.

Chas

Very impressive. Thank you for taking care of me and for the valuable service you offer.

Joann

Very professional environment in the heart of London to conduct studies that help discover the medicines of the future.

James

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Recruiting people with type 2 diabetes

Get paid $150 for your time in this study
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Duration of stay
You will need to attend an in-person visit, In total, you will come to the research unit at least once.
View trial dates
Ages
18-70
Location
London Bridge
Gender
Males & Females
Ethnicity
Any
Payment
£1,000
Ages
C23017
Smoking Restrictions
Smokers and non-smokers included
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Email us
Call: 020 7042 5800

Study Summary

We are conducting a study for participants with genetically diagnosed alpha-1 antitrypsin deficiency (Alpha 1) who are interested in participating in future gene editing clinical trials.
In this study, we are recruiting participants with Alpha 1 (with a known or suspected PiZZ mutation) aged 18 to 70. We will give you a tour of the clinical trials unit and conduct a number of clinical assessments to establish your current health status.
This study is to help participants with Alpha 1 decide if they want to participate in future gene editing clinical trials.

If you are interested in participating in this patient engagement study

  • You will need to attend an in-person visit, we will give you a tour of the clinical trial unit and perform tests to check your general health to obtain a clinical baseline.
  • The tests can be spread over multiple days (if required).
  • You will have a follow-up call with a doctor a week after the in-person visit.
  • This means the whole process takes approximately 1 week.

Who can take part?

We will check your suitability for the clinical trial using the following criteria:
  • You are aged between 18 to 70 years (inclusive).
  • You must have been diagnosed with alpha-1 antitrypsin deficiency (Alpha 1) (with a known or suspected PiZZ mutation).
  • You must be able and willing to provide informed consent.
  • You must be willing and able to comply with study assessments.
A full list of do’s and don’ts will be given to you by a member of our recruitment team if you are interested and want to find out more.

Study payment

In recognition of the time and effort involved in taking part in the study, you will receive £150 on completion of the study, provided you comply fully with all the study requirements.

Study dates

Following the completion of your registration form, a member of our recruitment team will contact you via phone and email to inform of the available dates.

Approval

The contents of this email have been approved by an ethics committee. Any response to this advertisement will be recorded. Your response will not place you under any obligation to participate in this trial.
You may be required to remain resident in the unit until resolution of any safety issues, after which you will be discharged from the unit.
Ref: C23017_MAR_2024 (email_website_advert text)
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Speak to a member of our Volunteer Recruitment Team

Call: 020 7042 5800