Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 12:35 PM
Ignite Modification Date:
2025-12-24 @ 12:35 PM
NCT ID:
NCT03875261
Eligibility Criteria:
Inclusion Criteria:
* Women between the ages of 18 and 40.
* Diagnosis of deep endometriosis after clinical suspicion and confirmation by imaging test.
* Pain with a score of 4 or more on a numerical visual scale of 11 levels (EVN 0-10) in the last 3 months (includes any type of pain associated with endometriosis: dysmenorrhea, dyspareunia, dyschezia, dysuria and / or pelvic pain).
* Women of childbearing age \* should have a negative pregnancy test before inclusion in the study and should commit to using highly effective contraceptive methods (hormonal contraceptives, intrauterine device, intrauterine hormonal release systems, bilateral tubal occlusion, vasectomy the couple, barrier methods and sexual abstinence) during the entire duration of the study and up to 3 months after the end of it.
* Acceptance of participation in the study by signing the informed consent.
Exclusion Criteria:
* Patients previously submitted to open abdominal surgery.
* History of cancer.
* Suspicion or diagnosis of endocrine, cardio-vascular or systemic pathology relevant.
* Pregnancy or anticipation of pregnancy up to 3 months after the end of the study.
* Current breastfeeding.
* Use of hormonal treatment (combined oral contraception, progestin in the 3 months prior to the study, GNRH analogs in the 6 months prior to the start of the study).
* Use of other analgesics different from those allowed in the study.
* Recreational or pharmacological use of cannabinoids.
* Hypersensitivity to cannabinoids or any of the exceptions.
* Known or suspected personal history, or family history of schizophrenia or other psychotic illnesses, severe personality disorder or other major psychiatric disorders.
* Patients with liver or kidney failure, severe cardiovascular disease and a history of epilepsy or recurrent seizures.
* Patients who use concomitant potent enzyme inducers of CYP3A4, such as rifampicin, carbamazepine, phenytoin, phenobarbital, and St. John's wort.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
40 Years
Study:
NCT03875261
Study Brief:
Protocol Section:
NCT03875261