In this Section:
Researchers at Austin LifeSciences often run clinical trials that need participants from the local community.
All clinical trials conducted at Austin Health are done so under Australian and International guidelines for medical research under the approval of Austin Health Human Research Ethics Committee (HREC).
If you are an Austin LifeSciences researcher and would like to list a trial here, please email a request with a copy of your HREC-approved advertisement to email@example.com
The Sleep Research Laboratory at University of Melbourne and the Institute for Breathing and Sleep at Austin Health are recruiting obstructive sleep apnoea patients, 30-45 years old, for a study on memory and mood.
Participation involves a 1.5 hour session at the Sleep Laboratory, where you will be asked to complete some questionnaires and memory tasks.
Participants will be reimbursed for their time. University of Melbourne HREC#1239101.
Enquiries: Melinda Jackson 90356129
Cancer Clinical Trials Centre (CCTC), at Austin Health, is the second largest cancer trials centre in Victoria, and one of the largest in Australia.
There are over 25 consultants actively participating in oncology and haematology clinical trials with a wealth of experience.
The department has specialised experience in Phase 1 to Phase 3 trials across all tumour streams (excluding sarcoma) including complex and first in human trials with a dedicated Phase 1 team.
There are over 250 trials in total with around 25% of these actively recruiting patients at any one time. Please follow the below link to discover what trials are currently open to recruitment: http://trials.cancervic.org.au/
If you answered "Yes" to any of these questions then you may like to get involved in Alzheimer's disease research
Participants may qualify if they are:
Jenny Kaiser : phone: 9496 2331 email firstname.lastname@example.org
Mitra Vazifdar: phone: 9496 2964 email email@example.com
MCRU Office: phone 9496 4235
Alternatively you can register you interest by sending an email to: firstname.lastname@example.org
The Department of Endocrinology is recruiting people for a drug trial comparing estradiol skin gel and a placebo skin gel (inactive medication).
Potential participants should be receiving androgen deprivation therapy to treat prostate cancer.
Participants in the study will be asked to attend Austin Health four times over a period of six months.
If you are interested and would like further information, please contact Dr Nick Russell on 03 9496 5000.
This study has been approved by the Austin Health Human Research Ethics Committee Reference Number HREC/16/Austin/98.
If you are about to start gender transition with hormone therapy (or a health volunteer not undergoing transition) you may be eligible to take part in a clinical research study. We are studying the changes that occur with hormone therapy on bone, fat, muscle and cardiovascular risk. The study involves questionnaires, bloods tests, and two scans (DXA/body composition and a bone CT).
We are looking for people:
- Age 18 years or older
- About to start gender transition
- Otherwise fit and healthy
- Not previously on gender affirming hormone therapy
- No previously diagnosed bone disease such as osteoporosis
- Willing to attend 5 visits over 2 years
- We are also looking for healthy volunteers (who are not undergoing gender transition)
If you choose to take part, you will be looked after by an experienced study team who will carefully monitor your health. You will continue to take any current medications.
For more information please contact: Dr Ingrid Bretherton on 9496 2486 or email: email@example.com
This study has been approved by the Austin Health Human Research Ethics Committee: HREC17Austin74
The Austin Endocrine Department, in collaboration with the Mercy Hospital for Women, is conducting a study looking at kidney function in pregnancy.
We are looking for women aged less than 40 who are planning pregnancy or under 12 weeks pregnant. Eligible women will have their kidney function measured prior to (if applicable), during and after pregnancy.
This project has been approved by the Austin Health Human Research Ethics Committee.
If you are interested in participating, please contact Dr Jenny Huynh (Endocrine Fellow) on 03 9496 2260 or firstname.lastname@example.org for further information.
The Parent-Infant Research Institute at Austin Health is conducting a study to evaluate a new internet-based treatment program targeted for women experiencing postnatal depression. If you feel you are struggling to cope or experiencing postnatal depression, this program may be of benefit to you.
Each participant receives a phone assessment with a psychologist to discuss treatment options and to link you in with support services.
Participants will be randomly allocated to receive either the Internet-based treatment (MumMoodBooster) program, or routine primary care.
Participants will be asked to complete questionnaires and phone assessments at three time points over three months.
Each participant will be reimbursed for their time completing the questionnaires and for a telephone assessment interview ($35 in total).
The Internet-based treatment is free of charge.
This study has been approved by the Human Research Ethics Committee of Austin Health. For more information and eligibility criteria, contact the Parent-Infant Research Institute on 9496 4496 or email@example.com.
You may be interested in participating in a clinical trial of a new medication for PTSD called N-acetylcysteine (NAC). NAC is derived from a naturally occurring substance with antioxidant properties.
If you are eligible for the trial, you will be randomly allocated to receive either active NAC or an inactive placebo to take 3 times per day for 12 weeks, while you continue your other treatment as usual. You will be asked to attend 6 appointments at the Psychological Trauma Recovery Service (PTRS) at the Heidelberg Repatriation Hospital in Ivanhoe, where your PTSD symptoms and related difficulties will be assessed by questionnaires and interview.
The research is being conducted by the department of psychiatry at the University of Melbourne and Austin Health. This trial has been approved by the Austin Health Human Research Ethics Committee. HREC/16/Austin/188.
If you are interested in participating, or want to know more, please contact our researcher Anita Dharan : 9496 2624. Anita.DHARAN2@austin.org.au
To all Stroke Survivors,
You are invited to take part in this research project because you have suffered a stroke in the past. The purpose of this research project is to understand the effects of a short exposure to virtual patient room designs on the emotional, cognitive, and physical responses of people with stroke. This is being done to enable us to better design hospital and rehabilitation environments for people recovering from stroke.
1. Where is the study held?
All investigations will be carried at the Austin Hospital and the Melbourne Brain Centre, Florey Institute of Neuroscience and Mental Health, which is on-site at the Austin Hospital Campus. A parking space will be reserved for you at the Melbourne Brain Centre, Austin Hospital Campus, for each visit.
2. What is the first step?
Please contact the named researcher (Michelle Shannon) listed below. The researcher can you send you a Participant Information and Consent Form (PICF). This document provides you with more detailed information about the aims of the study and what is involved. If you would like more information about the study, or you are interested in taking part, please telephone or email the study co-ordinators.
A collaborative study between Austin Health, Melbourne Health and Victoria University investigating a method of improving walking to reduce tripping in people who have had a stroke is currently seeking participants.
You may be eligible to participate if you:
What will you be asked to do?
If you feel you might be eligible and are interested in participating, please contact Joanne Quek for further information [phone: 9496 2659 or email: firstname.lastname@example.org ]
This study has been approved by the Austin Health Human Research Ethics Committee Reference Number HREC/15/Austin/516.
If yes, we are seeking volunteers with type 2 diabetes who are interested in participating in a placebo-controlled weight loss research study of an investigational medication.
You may qualify for the trial if:
For more information or to see if this trial is suitable for you, please contact Research Coordinator, Austin Health, Nicky 9496 2645 or email: ClinicalTrials-UoMrepat@unimelb.edu.au
This research study has been approved by the Austin Health Human Research Ethics Committee (HREC ZAF-203)
Research into Preventing Diabetes Type 2 using Testosterone & Healthy Lifestyle
Free access to Weight Watchers
The Department of Medicine at Austin Health is recruiting men aged 50-74 years, with a waist circumference of 95cm or greater.
Participants would need to be available every 3 months for injection of testosterone or placebo & blood tests.
For further information or to screen yourself for eligibility go to: www.t4dm.org.au click on Join T4DM & complete questionnaire
or contact Jenny Healy on 03 9496 2282 or email t4dm-Austin@unimelb.edu.au
This trial has been approved by the Austin Health Human Research Ethics Committee