Study of Real Clinical Practice to Evaluate the Effects of Oral Dydrogesterone for Treatment of Confirmed Endometriosis
Launched by ABBOTT · Sep 28, 2018
Trial Information
Current as of August 11, 2025
Completed
Keywords
ClinConnect Summary
A non-interventional, observational program to assess the effects of oral dydrogesterone therapy in a post-marketing setting whether the effects are related to the regimen of dydrogesterone therapy. In this observational program, assuming that dydrogesterone plays a role in the treatment of endometriosis without suppression of ovulation, the goal is to observe the possible implications of such treatment in terms of treatment regimen and response pattern. In the study will be described effects of Duphaston® 6-months-administration in patients with confirmed endometriosis by assessing pain re...
Gender
FEMALE
Eligibility criteria
- Inclusion Criteria:
- • Female, aged ≥ 18 years and ≤ 45 years.
- • Complaints on chronic pelvic pain with or without dysmenorrhea assessed by 11-items NRS.
- • External genital endometriosis confirmed by laparoscopy.
- • Existing pelvic (vaginal) ultrasound data not earlier than 2 months before inclusion in the study.
- • Prescribed treatment with Duphaston® according local labelling for treatment of endometriosis 10 mg 2-3 times a day from the 5th to the 25th day of the menstrual period cycle or continuously.
- • No hormonal treatment in 2 cycles before enrollment.
- • Signed Patient Authorization for Use/Disclosure of Data.
- Exclusion Criteria:
- • Any co-existing disease(s) needing chronic drug therapy (e.g. Crohn's disease, diabetes etc); Severe concomitant medical illness.
- • Severe other genital pathology excluding endometriosis (e.g. Multiple/severe myoma; adenomyosis, inflammatory diseases, etc.).
- • Routine consumption of analgesics other than for the pain of endometriosis.
- • Patients receiving hormonal contraceptives in last 2 cycles (including intrauterine devices, contraceptive patches, contraceptive rings, oral contraceptives etc.).
- • Ongoing pregnancy.
- • Menopause or premature ovarian failure.
- • Contraindications to dydrogesterone treatment listed in the locally approved label (Instructions for the medical use of Duphaston®).
- • Any other condition that precludes use of dydrogesterone in a particular patient, in accordance with the precautions and special warnings listed in the locally approved label (Instructions for the medical use of Duphaston®).
- • Abnormal results of pap smear test.
- • Other conditions that made the patients participation impossible (based on the investigator decision).
- • Fertility treatments using assisted reproductive technology.
About Abbott
Abbott is a global healthcare company dedicated to improving lives through innovative medical technologies, diagnostics, nutrition, and branded generic pharmaceuticals. With a commitment to advancing health and wellness, Abbott conducts clinical trials to evaluate the safety and efficacy of its diverse portfolio of products, which span multiple therapeutic areas, including cardiovascular, diabetes care, and neurology. The company employs rigorous research methodologies and collaborates with healthcare professionals and institutions worldwide to ensure the highest standards of clinical integrity and patient safety. Abbott's mission is to deliver impactful solutions that enhance patient outcomes and contribute to the advancement of global healthcare.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Chelyabinsk, , Russian Federation
Ekaterinburg, , Russian Federation
Engel's, , Russian Federation
Kazan, , Russian Federation
Kemerovo, , Russian Federation
Krasnodar, , Russian Federation
Krasnoyarsk, , Russian Federation
Krasnoyarsk, , Russian Federation
Moscow, , Russian Federation
Moscow, , Russian Federation
Novgorod, , Russian Federation
Novosibirsk, , Russian Federation
Rostov On Don, , Russian Federation
Saint Petersburg, , Russian Federation
Saint Petersburg, , Russian Federation
Stavropol', , Russian Federation
Tyumen, , Russian Federation
Ufa, , Russian Federation
Voronezh, , Russian Federation
Voronezh, , Russian Federation
Patients applied
Trial Officials
Andrey V Kozachenko, Prof
Study Chair
Kulakov National Medical Research Center of Obstetrics, Gynecology and Perinatology
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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