Participate in a clinical trial

Invest in your own health, and the health of future generations

Why participate in a clinical trial?

Clinical trials are an essential step in the development of new drugs and therapeutic options for today’s patients and tomorrow’s population.

We run research trials in a broad range of therapeutic areas and are always looking for participants.

​There are many reasons to participate in a clinical trial at CGM Research:

  • You will be helping develop treatment options for patients with your condition.
  • You will have regular thorough assessments with our skilled nursing and medical staff.
  • You will learn more about your condition and available therapies.
  • You may have access to drugs and treatments not yet available to the public.
  • You will have medical tests relevant to your condition.
  • With your permission we will communicate with your GP.
View Current Trials
participate in a clinical trial

What is a
clinical trial?

For the placebo-controlled explanation “As a new drug is developed, there is usually a phase where it is tested against placebo. A placebo is sometimes referred to as a “sugar pill” and it should have no particular therapeutic effect.

Some trials will involve comparing one group of patients who are on active drug and another group who are taking placebo. In general neither the patient nor the team at CGM will know who was who until the end of the trial. All other assessments and treatments will be identical for each group.

This kind of trial design is very powerful in determining if a new treatment is truly effective.

This very much depends on the trial, but in any trial you will never be left out of pocket.

Any reasonable expenses such as transport and accommodation will be covered and paid into your account directly. Some studies will have specific compensations for specific aspects of the protocol and these will all be made clear to you by the team at CGM.

Some studies involve so called “Healthy Volunteers” who have no particular medical condition or symptom. These studies will generally compensate for all the time that is involved for the participant.

Clinical trials are scientific studies involving human volunteers or participants, designed to assess safety and efficacy of new treatments and add to medical knowledge.

​A Clinical Trial is conducted to find better ways to prevent, diagnose and treat diseases. Clinical Trials are one of the final stages in a long and careful research and development process to find new and better health care solutions. Trials of new potential treatments may show which medical approaches are better for different illnesses or groups of people.

All medicine and treatments must be tested in clinical research studies before they can be approved by regulatory authorities and made available for use. Without clinical trials and clinical trial participants there would be no new medicines or treatments.

All trials must meet strict Ministry of Health guidelines, they must also be approved and monitored by the New Zealand Ethics Committee and other governing bodies for the duration of the trial to ensure all participants are appropriately treated.

View Current Trials

Trial phases

What are clinical trials?

All new drugs for treatment in humans must pass through several phases of clinical trials.

  • Testing on a small number of healthy volunteers to check safety, efficacy and tolerability and determine side effects.

  • Establishing the efficacy of the drug, usually against a placebo, on patients with the condition the medication is designed to treat.

  • These trials involve large numbers of participants to assess treatment efficacy, effectiveness and safety.

  • Once a treatment is on the market, further trials are conducted to compare trials, assure long-term safety and effectiveness of the drug.

CGM Research Trust pays careful attention to the needs of participants, throughout the course of the study providing services such as transportation, 24 hours availability of study staff, arrangement of referrals to other doctors and support groups and ensuring continuity of care.

Frequently
asked questions

A clinical trial is conducted to find better ways to prevent, diagnose and treat diseases. Trials of new potential treatments may show which medical approaches are better for different illnesses or groups of people.

A clinical trial is designed to find which treatments are most effective.

A clinical trial is one of the final stages in the long and careful research and development process to find better healthcare solutions.

There are very strict guidelines and safeguards to protect participants in clinical trials.

Whilst in a clinical trial, participants are seen regularly by the research team to monitor their health and to determine the safety and effectiveness of their treatment.

Governing bodies and independent review boards oversee all studies and ensure risks are as low as possible.

Trials may be sponsored by pharmaceutical companies, biotech agencies, medical research institutions, foundations or trust organisations

A protocol is a study plan carefully designed to safeguard the health of the participants and answer specific research questions.

The protocol describes the purpose of the trial, how it will be performed, the types of people who can participate, the schedule of tests, procedures, medications, and the length of the study.

Informed consent is the process by which an individual voluntarily confirms their willingness to participate in a particular trial.

You will be given a copy of the informed consent document, which contains information regarding all aspects of the trial.

The informed consent form states why the research is being done, what will happen during the study, the time involved, the risks and benefits, your rights as a participant and how your privacy will be protected.

An informed consent form must be signed before any study procedures can be undertaken.

The results will be made available to you when the trial has been completed.

All clinical research studies have guidelines called eligibility criteria which determine who can participate.

These guidelines are based on factors such as age, medical history, current medical conditions and medications.

These criteria are used to identify suitable potential participants.

Trials vary in length and time requirements.

All this will be fully explained to you before you decide whether or not to participate.

Involvement in clinical research trials is voluntary.

You are able to change your mind and withdraw at any time.

Withdrawal will not affect any future medical care

All trial participants are protected by the Health and Disability Act Code of Rights.

There are very strict international standards and regulations for all trials involving human participants.

All your medical records and information will remain completely confidential.

A placebo is an inactive substance that has no therapeutic effect.

In clinical trials experimental treatments are often compared with a placebo to assess the effectiveness of the treatment.

This varies depending on the trial.

You will be reimbursed for your expenses while participating in the trial e.g. travel costs.

The CGM Research staff are happy to answer all your questions

You can talk to your own doctor or specialist

You can also contact the Health & Disability Committee (HDEC), ph. 0800 384 427

For more information on Certified Clinical Trial Sites go to the Medsafe Website.

Sponsors + Partners

 
PreviousNext

Privacy Policy
Cookie Policy

+64 3 365 6777
enquiries@cgm.org.nz
Level 3, 800 Colombo Street
Christchurch Central City
Christchurch, 8013

For Participants
For Sponsors
About CGM Research Trust
Current Trials
Contact Us

©2024 CGM Research Trust Ltd.  |   Website Developed by Happy Monday Ltd

CGM Research Instagram
CGM Research on Facebook