Clinical Trials

Current Clinical Trials for Women

Arizona Gynecology Consultants is proud to offer the opportunity for our patients to participate in research that promotes knowledge, understanding, and well-being of women. Below you will find a list of current clinical trials and research studies for which we are actively recruiting participants.
Women Research
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EndoCheck

For our patients undergoing a diagnostic laparoscopy to be evaluated for endometriosis they are eligible to participate int eh Aspira Labs/ “Deep neural network stratification for the use of detecting Endometriosis in women affected by chronic pelvic pain”. Your participation in this research is voluntary. If you choose to participate, the study will last approximately 3 months, with two visits to the study site (our office). You will read, sign, and date this informed consent form. We will gather information from your medical history (such as prior surgeries and current medications), have you complete the Endometriosis Health Profile Questionnaire, and then we will collect a sample of your blood. After your surgery, we’ll have you complete the Endometriosis Health Profile Questionnaire again (only if you were confirmed to have endometriosis) and we will compare the results of the blood study test to the results from your gynecological surgery.
If interested, please contact your Surgeon at Arizona Gynecology Consultants for further information.
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Rejoni

Have you been told that you have intrauterine adhesions or fibroids? We are offering a clinical trial that is evaluating a new product that may prevent them.
What are intrauterine adhesions?
Intrauterine adhesions are commonly referred to as “Asherman’s Syndrome”, they are bands of fibrous tissue that form in the uterus, often after a uterine procedure (D&C’s, hysteroscopy). These adhesions can cause pelvic pain, light menstrual periods, prevent pregnancy, and/or cause miscarriages.

In this study, potential participants are those who are undergoing uterine surgery either to remove fibroids or to disrupt existing adhesions in a procedure called adhesiolysis. Qualified participants will be randomly assigned to either receive instillation of the hydrogel (treatment group) directly after completion of the uterine surgery or to not have the hydrogel instilled (control group). Two women will be assigned to the treatment group for every one assigned to the control group.

If you are interested in this research trial please book an appointment with a Arizona Gynecology Consultant provider to see if you are a good candidate.

IUAs

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