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MiGel Study 

The MiGel study is a clinical trial to investigate the potential effect of a topical medication for the treatment of vulval/vaginal pain with sexual activity. 

Participants in the study need to be living in Australia, women aged 30 and over who also; 

  • have experienced pain in or around the vulva/vagina during sex for at least 3 months, 
  • are currently sexually active (including with self) or would like to be but can’t because of pain, 
  • have given birth at least once with no severe morning sickness, and 
  • are NOT currently pregnant or breastfeeding, and willing to avoid pregnancy during the study 

If you’re interested in participating in this study, please complete the survey below to check if the study is suitable for you and one of our team will contact you soon. 

Jump to survey

FAQs 

Which cream will I be using?

For the purpose of this study, you will be using either the active or placebo cream. For every three participants, two will receive the active cream and one will receive the placebo cream

How much of my time will the study require? 

If the study is suitable for you, our team will contact you. We will then email you the Patient Information and Consent Form, which takes approximately 10 -15 minutes to read. Next, we will arrange a 30 minute telehealth appointment with our study clinician.  Once enrolled, you will participate in the study for 12 weeks.  

There is one quick question to answer online each week, that should take less than one minute to complete. 

There are 4 sets of survey questions to complete:

  • two longer questionnaires, one before you start the study, and a final one at 12 weeks  
  • two shorter questionnaires at 4 and 8 weeks.  

We estimate the longer surveys to take between 20-40 minutes, and the shorter surveys will take approximately 15 minutes to complete. Surveys are online so you can use your smartphone/computer. 

The time estimated for the application of the study cream is about 2 minutes, twice a day including time to wash the syringe. We will provide a short video demonstration (3 minutes) on how to apply the cream and instructions on how to fill in the surveys. 

What are the costs involved? 

Participants will receive compensation for time and inconvenience associated with the study.  

Do I have to travel to the clinic? 

No. All study visits are telehealth, so there is no travel involved. 

For healthcare providers 

If you are a healthcare provider considering referring a patient to this study and would like more information, please contact research@whria.com.au 

Principal Investigator: Dr Karen Chan
Women’s Health & Research Institute of Australia 
Level 12/97-99 Bathurst St, SYDNEY, NSW 2000
Study sponsor: TA Pharma Pty Ltd 

Study recruitment survey

I am female aged 30 or older?(Required)
I have experienced pain in or around the vulva/vagina during sex for at least 3 months.(Required)
I am currently sexually active (including with self) or would like to be but can’t because of pain.(Required)
For this study sexual activity includes vulval contact of any type, such as toys, fingers, genitals, oral sex.
I have given birth at least once with no severe morning sickness.(Required)
I am NOT currently pregnant or breastfeeding, and willing to avoid pregnancy during the study.(Required)
I have had a normal check-up of the genital area by a healthcare provider in the last 3 months (or I am willing to).(Required)
I am willing and able to apply a cream on the vulval area twice a day for 12 weeks.(Required)
I am willing and able to test vulval pain via one finger inserted in the vaginal entry.(Required)
At 4, 8 and 12 weeks, if you have not been sexually active for the previous 4 weeks.
I am prepared to complete weekly surveys for this study.(Required)
A 1-minute questionnaire every week, and a longer one before you start the study, and at 4, 8 and 12 weeks. Via smartphone, computer or on paper. Estimate about 10-15 minutes each. You will require adequate English skills to complete these surveys
I have no history of breast or genital cancer in the last 10 years.(Required)
Name(Required)

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