Actively Recruiting
Risk Factors for Non-response to Hormonal Medical Therapy in Patients With Endometriosis
Led by IRCCS Azienda Ospedaliero-Universitaria di Bologna · Updated on 2024-08-01
250
Participants Needed
1
Research Sites
292 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Determine the proportion of patients with endometriosis unresponsive to medical therapy and to compare the clinical and ultrasonographic characteristics of this group of patients (study group) with the clinical and ultrasonographic characteristics of patients responsive to medical therapy (control group).
CONDITIONS
Official Title
Risk Factors for Non-response to Hormonal Medical Therapy in Patients With Endometriosis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 18 and 50 years
- Patients with endometriosis-related pain symptoms such as dyspareunia, dyschezia, dysmenorrhea, chronic pelvic pain, dysuria, or periovulatory pain, with at least one symptom having a pain intensity greater than 5 on the Numerical Pain Rating Scale
- Indication for oral hormonal medical treatment for endometriosis
- Signed informed consent obtained
You will not qualify if you...
- Contraindications to oral hormone treatment
- Current or previous pelvic infections
- History of malignancy or suspicion of gynecologic malignant lesions
- Previous pelvic surgery including hysterectomy, salpingectomy, ovarian cyst removal, myomectomy, surgery for endometriosis, or bowel resections
- Positive history of other causes of chronic pelvic pain
- Post-menopausal status
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
IRCCS Azienda Ospedaliero-Universitaria, Policlinico Sant'Orsola
Bologna, BO, Italy, 40138
Actively Recruiting
Research Team
A
Alessandro Arena
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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