Relugolix and Dienogest for Endometriosis: Randomized Controlled Study

Not Applicable

Recruiting

• Conditions: endometriosis

• Registration Number: JPRN-jRCTs061230064
• Lead Sponsor: Taniguchi Fuminori

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2023-09-29
• Last Update Posted: 22 January 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 100

Inclusion Criteria

1)Premenopausal Japanese women aged 18 years or older at the time of informed consent.
2)Patients with endometriosis. However, the diagnosis must be made by one of the following methods. In the case of recurrence after surgical treatment of endometriosis, those diagnosed again with one of the following.
-Those diagnosed with endometriosis by laparotomy or laparoscopy performed within 5 years prior to VISIT1
-Those are shown an ovarian endometrioma by performed that MRI within 1 year prior to VISIT 1 or ultrasound (transvaginal, transabdominal or ransrectal) from VISIT 1 to VISIT 2
-Those who have been diagnosed with clinical endometriosis and have either Douglas cavity induration, restricted uterine mobility, or pelvic tenderness by internal or rectal examination performed from VISIT 1 to VISIT 2
3)Those with a maximum VAS score of >30 for endometriotic pelvic pain during the screening period, including more than one menstrual period.
4)Those who has dysmenorrhea or pelvic pain of moderate severity or greater on the B&B scale of VISIT 2
5)Those who have cyclic menstruation.
6)Those who agree on appropriate contraception on a daily basis from the time of informed consent throughout of the study.

Exclusion Criteria

1) Those who used sex hormones within 4 weeks prior to obtaining consent.
2) Those who used GnRH analogs within 12 weeks prior to obtaining consent.
3) Those who with ovarian endometrioma larger than 10 cm and age 40 years or older at the time of conducted image inspection.
4) Those who with a history of total hysterectomy or bilateral oophorectomy.
5) Those who with complications of undiagnosed abnormal genital bleeding.
6) Those who with lower abdominal pain due to irritable bowel syndrome or severe interstitial cystitis.
7) Those who with complications of pelvic infection.
8) Those who with malignant tumors.
9) Those who with a history or complications of severe hypersensitivity or severe adverse reactions to Relugolix or Dienogest.
10) Those who is pregnant, lactating, planning to become pregnant between the time of informed consent and one month after the completion of the study, or planning to donate eggs during this period.
11) Those deemed by the principal investigator or subinvestigator to be inappropriate to participate in this study.

Study & Design

• Study Type: Interventional
• Study Design: Not specified