View all studies | Endometriosis

Endometriosis Clinical Trial

Endometriosis is a common but often painful condition that happens when tissue similar to the lining of the uterus grows outside of it. This can lead to symptoms such as pelvic pain, heavy periods, and, in some cases, difficulties with fertility. Endometriosis pain can affect daily life and well-being in many ways, and finding relief isn’t always easy.

We’re conducting clinical trials to assess the safety and effectiveness of an investigational non-hormonal medication that may potentially help reduce pain in premenopausal women with moderate to severe endometriosis-related pain.

If you have been diagnosed with endometriosis and experience uncontrolled moderate to severe pain despite taking medications, then one of our clinical trials may be suitable for you.

Eligible participants may:

Receive regular monitoring at trial visits and access to our medical team if needed.
Help future generations by contributing to medical research.
Have the results of any additional investigations undertaken forwarded to their GP.

For further information and to discuss your eligibility with our team, please complete our online form.

Register your interest

Are you between the ages of 18 and 45? *

Yes

Is your BMI between 18-35? *

Yes

Have you had any of the following investigations for your endometriosis in the last 10 years: abdominal laparoscopy, transvaginal ultrasound (TVS/TV USS), or magnetic resonance imaging (MRI)? *

Yes

Do you take medication for your endometriosis but still experience pelvic pain outside your menstrual cycle? *

Yes

First Name *

Last Name *

Email Address *

Phone Number (inc area code) *

Address (Town / City) *

Post Code *

Select your nearest clinic *

How did you hear about this trial? *

When you register your interest with Accellacare (which is part of ICON plc), our team will review your information and connect you with studies that you may be eligible for. When we find a match, Accellacare clinical research specialists will contact you directly for further pre-screening. Please see our Privacy Policy for further details.

Data Protection

ICON plc is the data controller of the personal data, including health data, race and ethnicity, you choose to provide. We rely on your consent to use this information to identify potentially appropriate clinical trials for you, contact you about them, and to allow us to measure diversity of enrolment within clinical trials and support clinical trial access and diversity. When we call you for further pre-screening, note that these calls will be recorded.

You can withdraw your consent at any time, for example by following instructions to do so in emails or SMS you receive from us, or by telling our patient recruitment team when speaking with them. This does not affect the lawfulness of the processing prior to your withdrawal. Additional information on how your data will be processed and how you can exercise your rights, can be found in our Privacy Policy.
Please confirm if you consent to ICON plc collecting and using your personal data for the above purposes. *

I Agree

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Please note: You may or may not benefit medically from taking part and you are able to opt-out at any time and do not have to give us a reason for doing so. Your GP will be informed about your participation and all medical assessments that will be carried out as part of the trial. If during screening any abnormal results are found, you and your GP will also be informed.