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Endometrial Polyps Regression With Progesterone Therapy

Primary Purpose

Endometrial Polyp

Status
Unknown status
Phase
Phase 3
Locations
Italy
Study Type
Interventional
Intervention
subcutaneous progesterone
Sponsored by
University Magna Graecia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Endometrial Polyp

Eligibility Criteria

18 Years - 50 Years (Adult)FemaleAccepts Healthy Volunteers

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

Sites / Locations

  • Ospedale Pugliese CiaccioRecruiting
  • Federico II UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

watch-and-wait patients

Progesterone patients

Arm Description

patients who receive a watch-and-wait approach

Treatment consists of 7 days of 25 mg subcutaneous progesterone administered from 18° to 25° day of the menstrual cycle and repeated for 3 cycles

Outcomes

Primary Outcome Measures

Polyps regression rate
US evidence of normal endometrial line without evidence of polyps

Secondary Outcome Measures

Polyps dimensions
Effect of progesterone on polyps dimensions measured in mm
Correlation between polyps dimension and regression
Correlation between the size of the polyps and the efficacy of progesterone therapy in terms of regression of lesions
Side effects
Evaluation of any side effects
Progesterone effects on menstrual bleeding assessed with PBAC (Pictorial blood loss assesment chart) score
Effect 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.

Full Information

First Posted
October 9, 2017
Last Updated
January 12, 2019
Sponsor
University Magna Graecia
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1. Study Identification

Unique Protocol Identification Number
NCT03309709
Brief Title
Endometrial Polyps Regression With Progesterone Therapy
Official Title
Efficacy of Subcutaneous Progesterone in Premenopausal Woman With Endometrial Polyp: a Multicentric Randomized Control Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2019
Overall Recruitment Status
Unknown status
Study Start Date
October 8, 2017 (Actual)
Primary Completion Date
October 30, 2019 (Anticipated)
Study Completion Date
December 30, 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Magna Graecia

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Endometrial Polyp

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
watch-and-wait patients
Arm Type
No Intervention
Arm Description
patients who receive a watch-and-wait approach
Arm Title
Progesterone patients
Arm Type
Experimental
Arm Description
Treatment consists of 7 days of 25 mg subcutaneous progesterone administered from 18° to 25° day of the menstrual cycle and repeated for 3 cycles
Intervention Type
Drug
Intervention Name(s)
subcutaneous progesterone
Other Intervention Name(s)
Pleyris
Intervention Description
25mg daily for 7 days
Primary Outcome Measure Information:
Title
Polyps regression rate
Description
US evidence of normal endometrial line without evidence of polyps
Time Frame
three months after the starting of treatment or of watch-wait approach
Secondary Outcome Measure Information:
Title
Polyps dimensions
Description
Effect of progesterone on polyps dimensions measured in mm
Time Frame
three months after the starting of treatment or of watch-wait approach
Title
Correlation between polyps dimension and regression
Description
Correlation between the size of the polyps and the efficacy of progesterone therapy in terms of regression of lesions
Time Frame
three months after the starting of treatment or of watch-wait approach
Title
Side effects
Description
Evaluation of any side effects
Time Frame
three months after the starting of treatment
Title
Progesterone effects on menstrual bleeding assessed with PBAC (Pictorial blood loss assesment chart) score
Description
Effect 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.
Time Frame
three months after the starting of treatment

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Roberta Venturella, MD
Phone
+390961883234
Email
venturella@unicz.it
First Name & Middle Initial & Last Name or Official Title & Degree
Gian Marco Miele, MD
Phone
+390961883234
Email
gianmarcomiele@live.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Roberta Venturella, MD
Organizational Affiliation
Magna Graecia University of Catanzaro
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ospedale Pugliese Ciaccio
City
Catanzaro
State/Province
Calabria
ZIP/Postal Code
88100
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Roberta Venturella, MD
Phone
+390961883234
Email
venturella@unicz.it
First Name & Middle Initial & Last Name & Degree
Gian Marco Miele, MD
Phone
+390961883234
Email
gianmarcomiele@live.com
First Name & Middle Initial & Last Name & Degree
Alberto Vaiarelli, MD
Facility Name
Federico II University
City
Naples
ZIP/Postal Code
80121
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gabriele Saccone, MD
Phone
00393394685179
First Name & Middle Initial & Last Name & Degree
Antonio Raffone, MD
First Name & Middle Initial & Last Name & Degree
Gabriele Saccone, MD
First Name & Middle Initial & Last Name & Degree
Antonio Raffone, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
29729409
Citation
Venturella R, Miele G, Cefali K, Lico D, D'Alessandro P, Arduino B, Di Cello A, Zullo F, Di Carlo C. Subcutaneous Progesterone for Endometrial Polyps in Premenopausal Women: A Preliminary Retrospective Analysis. J Minim Invasive Gynecol. 2019 Jan;26(1):143-147. doi: 10.1016/j.jmig.2018.04.023. Epub 2018 May 2.
Results Reference
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Endometrial Polyps Regression With Progesterone Therapy

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