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Clinical Trials/NCT03789123
NCT03789123
Unknown
Phase 4

Effects of Dienogest and Dienogest Plus Estradiol Valerate on Ovarian Reserve and Endometrioma Size

Bagcilar Training and Research Hospital1 site in 1 country710 target enrollmentJanuary 1, 2019

Overview

Phase
Phase 4
Intervention
Estradiol valerate/dienogest
Conditions
Ovarian Reserve
Sponsor
Bagcilar Training and Research Hospital
Enrollment
710
Locations
1
Primary Endpoint
Ovarian reserve
Last Updated
7 years ago

Overview

Brief Summary

Progesterone resistance in endometriosis is a known fact. The progestin derivatives used in endometriosis cause decidualization and atrophy of ectopic foci. Moreover, they inhibit neo-angiogenesis, provide suppress expansile/destructive growth facilitated by matrix metalloproteinases, and implantation of ectopic foci. The effect of drugs containing the estrogen-progesterone combination is mainly based on the inhibition of ovulation, decidualization and atrophy of ectopic foci. In estrogen-progesterone mechanism, it is known that estrogen has a progesterone receptor-enhancing effect, which may make progesterone more potent. Based on this, the investigators hypothesized that estrogen added to progesterone could lead to a further reduction in endometrioma size by various mechanisms which probably include the increased progesterone sensitivity in endometriosis. In addition, the investigators hypothesized that this therapy can alleviate the destructive effect of endometriomas on the ovarian reserve.

Registry
clinicaltrials.gov
Start Date
January 1, 2019
End Date
December 1, 2019
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Bagcilar Training and Research Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Study Group: At least one endometrioma greater than 3 cm, between 18-40 years of age, without surgical indication at the time of diagnosis, occasionally and intermittently controlled pain with NSAIDs or no pain symptom
  • Control Group: Patients with reproductive age without any ovarian cysts

Exclusion Criteria

  • suspicion of malignancy, irregular mentrual period, endocrine diseases, drug intake that may affect ovarian reserve in the last 6 months (i.e GnRH agonists), previous ovarian surgery, AMH levels under 2 ng/ml.

Arms & Interventions

Study Group (patients with OMA)

I) Untreated patients (n=142) II) Dienogest (n=142) III) Dienogest/Estradiol valerate+Dienogest (n=142)

Intervention: Estradiol valerate/dienogest

Control Group(patients without OMA)

I) Untreated patients (n=142) II) Dienogest/Estradiol valerate+Dienogest (n=142)

Intervention: Estradiol valerate/dienogest

Outcomes

Primary Outcomes

Ovarian reserve

Time Frame: up to 24 months

The investigators evaluate serum anti-Müllerian hormone (AMH) level(ng/mL) using commercial elisa kits and antral follicle count (number) using ultrasonography. The patients with higher ovarian reserve represent a better outcome.

Secondary Outcomes

  • Pain Score(up to 24 months)
  • Endometrioma Size(up to 24 months)

Study Sites (1)

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