Evaluation of Therapeutic Effect and Safety of Mifepristone in the Treatment of Adenomyosis

Phase 3CompletedNCT03520439

xinmei zhang134 enrolled

Overview

This clinical trial is designed to study the effectiveness and safety of mifepristone in the treatment of symptomatic adenomyosis with multi center, random, double blind and controlled clinical trials. This multicenter study is performed in 150 subjects who are diagnosed as adenomyosis . Twelve weeks of randomization, allocation concealment, double-blind, placebo-controlled, parallel grouping. Subjects are randomly assigned to one of two treatment groups and received one of the following treatments: 1. Mifepristone tablets of 10mg, 1 tablet daily, oral 2. Placebo, 1 tablet daily, oral

Adenomyosis is a common benign disease of Gynecology, with secondary progressive dysmenorrhea and menorrhagia as the main clinical manifestations, which seriously harm the physical and mental health of the patients. Most patients have the desire to retain the uterus. Therefore, the treatment of drug conservative treatment is dominant in the treatment of adenomyosis. However, the current clinical treatment of adenomyosis still has some limitations and needs to be improved. Therefore, it is imperative to expand the clinical medication of adenomyosis. Mifepristone is defined as a selective progesterone receptor modulator. Under specific conditions, it plays the role of anti progestin, inhibits endometrial proliferation, inhibits ovulation, and can cause reversible amenorrhea. In recent years, it has been widely used in of uterine leiomyoma and endometriosis. Adenomyosis is also closely related to hormone related diseases, especially endometriosis. At present, the study of mifepristone in the treatment of adenomyosis is more extensive in China. A large number of domestic literature reports that low dose mifepristone for the treatment of adenomyosis is safe and effective for the treatment of adenomyosis . During the treatment of mifepristone, most of the patients had amenorrhea, obviously alleviating dysmenorrhea and reducing the menstrual volume, reducing the uterine and lesion volume of the patients with adenomyosis . However, most of the domestic literature is a small sample case control study or retrospective study. There is no randomized double blind control study. There is no clinical study on the application of mifepristone to adenomyosis in foreign countries. Therefore, the clinical evidence is inadequate, and a high quality randomized controlled trial is still needed. The purpose of this study is to demonstrate the effectiveness and safety of mifepristone (10mg) in the treatment of symptomatic adenomyosis with multi center, random, double blind and controlled clinical trials. It is a new clinical study for the old medicine.

Study Type

INTERVENTIONAL

Conditions

Adenomyosis

Interventions

MifepristoneDRUG

Oral mifepristone 10mg (first menstrual third days), 1 times a day, 12 weeks, fasting or taking 2 hours after eating

PlaceboDRUG

Oral Placebo Oral Tablet 1# (first menstrual third days), 1 times a day, 12 weeks, fasting or taking 2 hours after eating

Eligibility

Sex: FEMALEMin age: 18 YearsMax age: 50 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. B-ultrasound or magnetic resonance imaging (MRI) examination confirmed that the subject has adenomyosis, and the uterus is less than 10 weeks of pregnancy; 2. Visual analogue scale (VAS) of adenomyosis-associated pain\> 0 points; with or without menorrhagia (PBAC≥100 points); 3. Women between 18 and 50 years old who currently have no childbearing requirements; 4. Normal or cervical cytology results without clinical significance (results within 6 months before the screening period); 5. Willing to choose a barrier method of contraception if contraception is needed; 6. Be tested voluntarily and sign the informed consent. 7. No menopause No menopause Exclusion Criteria: 1. HB\<90G/L 2. Undiagnosed abnormal vaginal bleeding or endometrial lesions; 3. Pregnancy and lactation women and those who are preparing to give birth when taking the medication or within 6 months of stopping the medication; 4. Malignant tumors (including the reproductive system and other systems); 5. The patients with severe heart, liver, kidney disease and adrenocortical insufficiency; 6. The results of follow-up laboratory test indicate abnormal clinical significance; 7. The allergic persons or those who have been allergic to multiple drugs, or are allergic to active ingredients or any excipients of the study drug; 8. Suffering from any disease or condition that may cause the study drug to alter absorption, accumulate excessively, affect metabolism, or change the excretion pattern; 9. Having clinically significant depression within the current or most recent year; 10. People who regularly take analgesics due to other underlying diseases; 11. Ketoconazole, itraconazole, erythromycin, rifampicin, corticosteroids (hydrocortisone, prednisone, dexamethasone, etc.), and some anticonvulsants (phenytoin, phenobarbital, carbamazepine, etc.), griseofulvin, non-steroidal anti-inflammatory drugs (aspirin, acetaminophen, etc.) that are being used and cannot be stopped during the study; 12. Previous use of hormone drugs, including: a. use of GnRH agonists within 6 months before the screening period; b. use of progestins or danazol and other long-acting hormones within 3 months before the screening period; c. use of oral contraceptive-like short-acting hormones within one month before the screening period; 13. Patients who participated in other clinical trials within 3 months before the screening, or who are considered inappropriate to participate in the study by other investigators.

Locations (1)

Women's Hospital of Zhejiang Medical University

Hangzhou, Zhejiang, China

Outcomes

Primary Outcomes

changes in chronic pelvic pain associated with adenomyosis

To evaluate the visual analogue scale (VAS) changes.By using 10-cm visual analogue scales (0 = no pain, 10 = worst pain). Women will be asked to give the pain score at each follow up (i.e.Baseline ,taking medicine for 1-month, 2-month, 3-month, post treatment 1- month )

Time frame: Baseline ,taking medicine for 1-month, 2-month, 3-month and post treatment 1- month（approximately 16 weeks）

Secondary Outcomes

changes in uterine bleeding

To evaluate the pictorial blood loss assessment chart (PBAC) changes

Time frame: Baseline ,taking medicine for 1-month, 2-month, 3-month and post treatment 1- month（approximately 16 weeks）

improvement of anemia

To evaluate the hemoglobin changes,

Time frame: Baseline ,taking medicine for 1-month, 3-month （approximately 16 weeks）

Size of uterus

To evaluate the uterine volume changes

Time frame: Baseline ,taking medicine for 1-month, 3-month （approximately 16 weeks）

Data from ClinicalTrials.gov

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