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EndometriosisNCT05976529

A Multicenter, Observational Clinical Study of Dydrogesterone

An observational study of Endometriosis and Endometriosis Ovary, run by Guangdong Women and Children Hospital at 1 site in China.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

The objective of this study was to investigate the efficacy and safety of dydrogesterone in the long-term management of ovarian endometriosis cyst after surgery. Read more about this study

Who is it for?
Ages 18 to 45 years, women only
Conditions the study is for
Endometriosis, Endometriosis Ovary
Type of treatment
Pill or oral medicine
How many people
400 participants
Where
1 siteChina
Study dates
1 Jan 2023to 31 Dec 2025
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 45 years
  • Women only
  • Adult

Study population: Patients aged 18-45 years after surgery for ovarian endometriosis cyst

Who may be able to join

  • Patients who had undergone laparoscopic ovarian cyst excision and were confirmed by pathological diagnosis as ovarian endometriosis cyst (pathology was completed in each central hospital).
  • Ovarian cyst >4cm.
  • Concomitant infertility.
  • Patients who fail to respond to medication.
  • American Society of Reproductive Medicine(ASRM) stages were II-IV.
  • No relevant therapeutic drugs, such as dydrogesterone, dienogest, GnRHa, etc., were used 3 months before treatment.
  • No combined endocrine diseases.

Who cannot join

  • Ovulation disorders, immune defects and genital development abnormalities caused by infertility.
  • Patients who are allergic to the drugs used in this study.
  • Patients with severe hepatorenal insufficiency or malignant tumor.
  • Those who took hormone medication within 3 months before the study date.

Trial locations and contacts

1 site in 1 country.

China1 site, 1 recruiting
  • Guangdong Women and Children Hospital

    Guanzhou, Guangdong, 511400

    Li Li, M.D., +8613631446859, lili-1406@163.com

    Recruiting

Other trials in China

About this study

Official title: Efficacy and Safety of Dydrogesterone After Operation of Ovarian Endometrial Cysts: a Multicenter, Observational Clinical Study

The objective of this study was to investigate the efficacy and safety of dydrogesterone in the long-term management of ovarian endometriosis cyst after surgery.

Read the detailed description

Endometriosis refers to the appearance, growth and infiltration of endometrial tissue (glands and stroma) in the lining of the uterine cavity and other parts of the uterus, and repeated bleeding, which causes pain, infertility and nodules or masses. Endometriosis is a common gynecological disease in Chinese female patients, and its incidence has been increasing in recent years, which seriously affects the fertility and quality of life of patients. The typical clinical manifestations of endometriosis mainly include dysmenorrhea, pelvic pain and dyspareunia. Dysmenorrhea is a common symptom of endometriosis, which is secondary and persistent. The pain is most severe on the first day of menstruation and disappears completely at the end of menstruation. Pain is mainly caused by endometriosis bleeding, which irritates the inflammatory response of local tissues. Endometriosis lesions secrete prostaglandins, which cause contracture of uterine muscles and aggravate dysmenorrhea. Ovarian endometriotic cysts are the most common and easily detected type of endometriosis. Its clinical manifestations include: 1) dysmenorrhea, affecting daily activities and life; 2) chronic pelvic pain; 3) pain during or after sexual intercourse; 4) often complicated with infertility; 5) ovarian endometriotic cyst formation by imaging examination; 6) elevated CA125.

According to the guidelines for the diagnosis and treatment of endometriosis (third edition) published by Chinese Journal of Obstetrics and Gynecology in December 2021, ovarian endometriosis cysts can be divided into medical treatment and surgical treatment. The indications for drug therapy were: 1) ovarian endometriosis cyst diameter <4cm; 2) have pelvic pain. The treatment drugs include oral contraceptives, progesterone analogues, gestrinone, gonadotropin-releasing hormone agonist (GnRHa) and traditional Chinese medicine. The indications for surgical treatment were: 1) the diameter of ovarian endometriosis cyst ≥4cm; 2) combined infertility; 3) pain medications are ineffective. In clinical practice, most patients lose the opportunity of drug treatment, or drug treatment is ineffective, and most patients need surgical treatment. Laparoscopic surgery is the first choice for surgical treatment, and cystectomy is recommended. However, surgical treatment can only remove the superficial lesions, and it is difficult to remove the deep lesions, which is easy to leave lesions. After surgery, affected by steroid hormones, the small lesions left are easy to relapse, leading to the characteristics of recurrent disease. Therefore, the recurrence rate of ovarian endometriosis cyst after conservative surgery is high, and it must be treated with drugs and long-term management after surgery.

In the postoperative drug management of ovarian endometriosis cyst, the first-line drugs are mainly progesterone analogues (dienogest), GnRH-a, dydrogesterone and so on. There is evidence that the continuous use of dienogest for 24 months after surgery can significantly reduce the recurrence rate of ovarian endometriosis cysts. Dienogest is a fourth-generation highly selective progesterone receptor agonist, which acts locally on endometriotic lesions, has no male, estrogen, glucose and mineralocorticoid activity, and does not affect metabolism. It is used in the first-line treatment of endometriosis. "In a German retrospective study, dienogest 2 mg daily for 60 months was effective in reducing endometriosis associated pelvic pain, and dienogest was well tolerated." However, ovulation was inhibited in most patients during dienogest treatment. For patients with fertility needs, menstruation returned to normal after stopping dienogest for 2 months. To pregnant element is the most common adverse drug reactions: frequent or long time of uterine bleeding (3.2%), insomnia (2.7%), acne (2.1%), nausea (2.1%), weight (2.1%), lower abdominal discomfort (1.6%), headache (1.6%), breast discomfort (1.1%), and depressed mood (1.1%). Therefore, it is not suitable to use dienogest for postoperative management in patients with ovarian endometriosis who are in urgent need of pregnancy after surgery. At present, the cost of dienogest in our country is relatively high, about 500 yuan for a box (28 tablets), and there will be a certain economic burden for ordinary patients.

"Dydrogesterone is similar in structure to conventional progesterone and has only progestogen activity without estrogen, androgen, or mineralocorticoid activity. It atrophies the ectopic endometrium, prevents the development of new endometriotic lesions, and does not inhibit normal endometrium or ovulation. The menstrual cycle is regular in the course of regular treatment with dydrogesterone, so normal pregnancy can be achieved during the treatment." An open, multi-center, post-marketing, observational clinical study in Japan showed that dydrogesterone could effectively inhibit the growth of ovarian endometriosis cysts and improve the total score of dysmenorrhea and the degree of dysmenorrhea pain. Studies have shown that long-term treatment of endometriosis with dydrogesterone after surgery for 12 months can significantly reduce endometriosis-associated pain, treat infertility, and prevent recurrence of the disease. A Japanese multi-center study showed that the incidence of adverse drug reactions of dydrogesterone was 31.8%, and the most common adverse event was uterine bleeding. Dydrogesterone endometriosis was effective, safe and clinically beneficial for patients. For patients in urgent need of pregnancy, natural pregnancy can still be achieved during postoperative medication.

Keywords
endometriosis, dydrogesterone, therapeutic effect evaluation, safety, dienogest
Medical subject headings
Endometriosis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT05976529
Study groupRoleWhat they receive
study groupFrom the 5th to 25th day of menstrual cycle, 10 mg dydrogesterone was taken orally twice a day for 3 menstrual cycles.
control groupAfter postoperative pathological diagnosis, oral dienogest was started, 4 weeks as a course of treatment, and 3 courses of continuous treatment were given.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Visual analogue pain score(VAS)

    The visual analogue scale (VAS) was used to evaluate the pain. It is widely used in clinical practice in China. The basic method is to use a swimming ruler of about 10cm in length, marked with 10 scales on one side, and "0" and "10" points on both ends, with 0 points indicating no pain and 10 points indicating the most severe pain that can be endured.

    Measured: before drug treatment and 3 months after drug treatment

  2. Endometriosis fertility index(EFI)

    EFI score of endometriosis refers to the evaluation of fertility in patients with normal semen in men and good ovarian reserve function in women without adenomyosis. The pregnancy rate was measured by quantifying the patient's age, the duration and type of infertility, and the function of the fallopian tubes, uterus, and ovaries. If the score is higher than 9, the patient can try natural pregnancy. If the score is 5-8 points, the patient can be monitored by fertility guidance, if not naturally pregnant, can be treated by IVF-ET. If the score is lower than 5 points, the patients can be directly treated by IVF-ET.

    Measured: before drug treatment and 3 months after drug treatment

  3. The Cox Menstrual Symptom Scale(CMSS)

    The Cox menstrual symptom scale (CMSS) was used to evaluate the severity of symptoms and the duration of dysmenorrhea. The scale included 2 parts, CMSS-severity (CMSS-S) and CMSS-duration (CMSS-T), with a total of 18 observation indicators. It included 17 symptoms including nausea, vomiting, loss of appetite, headache, vertigo and the duration of dysmenorrhea. All CMSS-S items were scored on a 5-point scale: 0 as no symptoms, 1 as mild, 2 as moderate, 3 as severe, and 4 as extremely severe. CMSS-T is also a 5-point scale: 0 for no symptoms, 1 for persistent \&lt; 3h, 2 for 3~7h, 3 for 7~24h, 4 for continuous \&gt; 24 hours.

    Measured: before drug treatment and 3 months after drug treatment

Secondary outcomes (4)
  1. Serum CA125

    In some infectious diseases, autoimmune diseases, gynecological benign diseases, malignant tumors can appear CA125 significantly increased.

    Measured: before drug treatment and 3 months after drug treatment

  2. Anti-mullerian hormone(AMH)

    AMH is an important index to evaluate AMH is an important index to evaluate the reserve function of ovarian.

    Measured: before drug treatment and 3 months after drug treatment

  3. Short form 36(SF36)

    The SF36 is a short questionnaire with 36 items which measure eight multi-item variables: physical functioning (10 items), social functioning (two items), role limitations due to physical problems (four items), role limitations due to emotional problems (three items), mental health (five items), energy and vitality (four items), pain (two items), and general perception of health (five items). There is a further unscaled single item on changes in respondents' health over the past year. For each variable item scores are coded, summed, and transformed on to a scale from 0 (worst possible health state measured by the questionnaire) to 100 (best possible health state).

    Measured: before drug treatment and 3 months after drug treatment

  4. The postoperative pregnancy of the patients.

    Patients were followed up by phone calls to find out whether they were pregnant.

    Measured: 3 months after drug treatment

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 Aug 2023
  2. Study start1 Jan 2023
  3. Primary completion30 Apr 2025 (estimated)
  4. Study completion31 Dec 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Retrospective
Enrolment
400 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05976529
Sponsor's protocol ID
GuangdongWCH-LiLi02
Status last verified
Oct 2023
First submitted
25 Apr 2023
Last updated
23 Oct 2023
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Endometriosis and Endometriosis Ovary, run by Guangdong Women and Children Hospital at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 23 Oct 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Li Li, M.D. (+86 13631446859, lili-1406@163.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Visual analogue pain score(VAS) (time frame: before drug treatment and 3 months after drug treatment). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Oct 2023.

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