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Endometrial Polyps Regression With Progesterone Therapy

Efficacy of Subcutaneous Progesterone in Premenopausal Woman With Endometrial Polyp: a Multicentric Randomized Control Trial

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03309709
Enrollment
90
Registered
2017-10-13
Start date
2017-10-08
Completion date
2019-12-30
Last updated
2019-01-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endometrial Polyp

Brief summary

This prospective randomized study will compare the regression rates of women managed with watch-and-wait approach and of those treated with 3 cycles of luteal 25mg subcutaneous progesterone from 18 to 25 days of menstrual cycle

Detailed description

In premenopause, 25% of endometrial polyps regresses spontaneously in 1 year. According to guidelines, given that most premenopausal polyps are not malignant, there is an option for expectant approach with no surgical intervention. Studies on the efficacy of medical treatments for endometrial polyps are also recommended by gynaecologic societies, with the aim of finding cost-saving not invasive strategies to manage this common pathology. Up to now, nobody has investigated the effect of progestin administration on polyps, but molecular and clinical data suggest that the antiestrogenic effect of this hormone can be exploited to increase and speed-up their regression rate. Our preliminary results on the effect of three months of progesterone demonstrated a regression rate of 47,5% in women treated vs 12,5% in those don't receiving treatment. Accordingly, in this prospective randomized study we aim to compare the regression rates of women managed with watch-and-wait approach and of those treated with 3 cycles of luteal 25mg subcutaneous progesterone from 18 to 25 days of menstrual cycle

Interventions

25mg daily for 7 days

Sponsors

University Magna Graecia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* ultrasound diagnosis of endometrial polyps no more than 30 days before the enrollment * signed informed consent

Exclusion criteria

* estrogenic and\\or progestinic therapy two months before the enrollment * tamoxifen therapy * pelvic inflammatory disease * gynaecologic neoplasia * previous chemotherapy and radiotherapy * autoimmune diseases, chronic disease, metabolic, and endocrine (hyperandrogenism, hyperprolactinemia, diabetes mellitus and thyroid disease) * menopause * Hypogonadotropic hypogonadism * drugs causing menstrual irregularities

Design outcomes

Primary

MeasureTime frameDescription
Polyps regression ratethree months after the starting of treatment or of watch-wait approachUS evidence of normal endometrial line without evidence of polyps

Secondary

MeasureTime frameDescription
Polyps dimensionsthree months after the starting of treatment or of watch-wait approachEffect of progesterone on polyps dimensions measured in mm
Correlation between polyps dimension and regressionthree months after the starting of treatment or of watch-wait approachCorrelation between the size of the polyps and the efficacy of progesterone therapy in terms of regression of lesions
Side effectsthree months after the starting of treatmentEvaluation of any side effects
Progesterone effects on menstrual bleeding assessed with PBAC (Pictorial blood loss assesment chart) scorethree months after the starting of treatmentEffect of progestogen therapy on symptoms possibly present in patients with endometrial polyps, assessed with PBAC (Pictorial blood loss assesment chart) score. Patients will be asked to fill in the PBAC score during the first menstrual period following diagnosis and during the three months of medical treatment or watch and wait approach. The 8-days PBAC score is an objective method used to quantify menstrual blood loss; according to this method, each patient records the extent of uterine bleeding during the first 8 days of menstrual cycle, quantizing it in terms of daily change in diapers and number/size of the clots. Each option has a numeric value (1=no bleeding; 2=spotting; 3=1-8 diapers per day; 4=heavy bleeding) and, based on the result obtained, the monthly PBAC score varies from 0 (amenorrhea) to \> 500 (heavy bleeding). Menorrhagia occurs when PBAC score is \>100 during a menstrual cycle, corresponding to a blood loss greater than 80 ml.

Countries

Italy

Contacts

Primary ContactRoberta Venturella, MD
venturella@unicz.it+390961883234
Backup ContactGian Marco Miele, MD
gianmarcomiele@live.com+390961883234

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026