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Vitamin D for Polycystic Ovary Syndrome Clomiphene Resistant Women

Primary Purpose

PCOS, Vitamin D Deficiency

Status
Completed
Phase
Phase 4
Locations
Egypt
Study Type
Interventional
Intervention
Vit D
Metformin
Clomiphene
Sponsored by
Ain Shams University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for PCOS

Eligibility Criteria

20 Years - 35 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosis of PCOS as defined by the Rotterdam criteria
  • Females age 20-35 years old
  • BMI 18-30 kg/m2
  • 1ry or secondary infertility
  • Clomiphene resistant ( patients didn't - show response: ovulate to dose of 200 mg clomid per day for 3 cycles )
  • Willingness to comply with study protocol for 5 months
  • Willingness to give written informed consent to participate in the study

Exclusion Criteria:

  • Previous metformin intake
  • ovarian drilling
  • tubal factor as evidenced by hysterosalpingogram or laparoscope
  • endometrial pathology ex., polyp
  • Myometrial pathology ex., adenomyosis or fibroid
  • abnormal semen parameters
  • Cushing syndrome
  • Hyperprolactinemia
  • Adrenal secreting tumor

Sites / Locations

  • Ain Shams University Maternity hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Vitamin D

Control

Arm Description

Group V : number of 60 women will receive 100000 IU Cholecalciferol Intramuscular every month + 2000 mg Metformin (oral: 2 tablets 1000 per day) for 5 months . -after two months from the start: Clomiphene citrate 100mg (2 tablets clomid 50mg each per day,from 2nd to 6th day of the cycle ) will be added every month starting from the 3rd month to the 5th month .

Group C: number of 60 patients will receive Metformin 2000mg (oral: 2 tablets1000 mg per day) for months . -after two months from the start: Clomiphene citrate 100mg (2 tablets clomid 50mg each per day, from 2nd to 6th day of the cycle ) will be added every month starting from the 3rd month to the 5th month .

Outcomes

Primary Outcome Measures

Follicle growth and maturation
Transvaginal ultrasound will be done every 48 hours at the start from day 10 of the cycle to assess if the follicle reaches 17-19 mm
Change in Follicle growth and maturation at 3rd month
Transvaginal ultrasound will be done every 48 hours at the start from day 10 of the cycle to assess if the follicle reaches 17-19 mm
Change in Follicle growth and maturation at 5th month
Transvaginal ultrasound will be done every 48 hours at the start from day 10 of the cycle to assess if the follicle reaches 17-19 mm

Secondary Outcome Measures

Occurence of Chemical pregnancy occurence
Positive pregnancy test

Full Information

First Posted
July 2, 2019
Last Updated
July 3, 2019
Sponsor
Ain Shams University
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1. Study Identification

Unique Protocol Identification Number
NCT04010942
Brief Title
Vitamin D for Polycystic Ovary Syndrome Clomiphene Resistant Women
Official Title
Therapeutic Effect of Vitamin D3 Supplementation to Clomiphene Citrate Resistant Polycystic Ovary Syndrome Women
Study Type
Interventional

2. Study Status

Record Verification Date
July 2019
Overall Recruitment Status
Completed
Study Start Date
April 1, 2018 (Actual)
Primary Completion Date
December 30, 2018 (Actual)
Study Completion Date
March 30, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ain Shams University

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 study is determining the therapeutic effect of Vitamin D supplements to Pcos clomiphene resistant polycystic ovarian syndrome Women. Half of patients will receive Vitamin D with metformin while other half metformin only. Then both groups start clomiphene for 3 month
Detailed Description
Polycystic ovary syndrome (PCOS) is considered one of the most common endocrine disorders affecting women in their reproductive age. Genetically it is thought to be involving defects in primary cellular control mechanisms resulting in expression of chronic anovulation and androgen excess. Being familial condition , some researches showed it is autosomal dominant while others thought it is complex trait with oligogenic basis. Diagnosing poly cystic ovary syndrome is based on finding two of three criteria according to Rotterdam consensus 2003 : oligo/anovulation, clinical/ biochemical signs of hyperandrogenism, ultrasound finding of polycystic ovaries. While insulin resistance which affects 50 - 70 % of PCOS patients is considered to be the main reason for hyperandrogenic features, PCOS also leads to various health problems including metabolic disorders (obesity - Diabetes Mellitus - Cardiovascular diseases) in addition to menstrual irregularities and infertility . In PCOS women there is polymorphism in Vitamin-D receptor (VDR) gene associated with vitamin D level in blood . This gene is isolated from the female reproductive organs . In VDR null mice; uterine hypoplasia, impaired folliculogenesis and infertility is noted . That's why it is thought to be contributing in the genomic regulation of reproduction. Several studies have investigated the effectiveness of Vitamin D supplementation to PCOS women they found that PCOS women have hypovitaminosis D3 , with increasing evidence that vitamin D affects insulin and glucose metabolism . vitamin D intake in PCOS women may improve hormonal profiles in addition to having anti-inflammatory and anti-oxidant effects . Another study concluded that Vitamin D and calcium supplementation to PCOS women have a positive effect on BMI, follicular maturation, regularity of menses, androgen related symptoms, infertility and insulin resistance . Moreover, Vitamin D has a crucial role in ovulation induction in women with PCOS. Vitamin D and calcium in combination with metformin have significant effect on menstrual regulation and follicular development. Insulin sensitizers such as metformin have been extensively investigated in the management of PCOS. Metformin decreases blood glucose levels by enhancing peripheral glucose uptake, decreasing intestinal glucose absorption and suppressing hepatic glucose levels. In anovulatory women with PCOS, metformin decreases insulin levels, luteinizing hormone (LH) production and circulating androgen levels. Clomiphene citrate is an estrogen agonist and antagonist. It works by competitively binding estrogen receptors in the thalamus and as it remains in place for an extended period of time, it depletes the body's estrogen concentration at the hypothalamic level. As the body perceives low levels of estrogen, gonadotropin-releasing hormone (GnRH) is released which in turn stimulates pituitary release of follicle stimulating hormone ( FSH) which promotes follicular growth and maturation. If pregnancy is not achieved by 3-6 cycles, other treatments should be considered.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
PCOS, Vitamin D Deficiency

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Vitamin D
Arm Type
Active Comparator
Arm Description
Group V : number of 60 women will receive 100000 IU Cholecalciferol Intramuscular every month + 2000 mg Metformin (oral: 2 tablets 1000 per day) for 5 months . -after two months from the start: Clomiphene citrate 100mg (2 tablets clomid 50mg each per day,from 2nd to 6th day of the cycle ) will be added every month starting from the 3rd month to the 5th month .
Arm Title
Control
Arm Type
Placebo Comparator
Arm Description
Group C: number of 60 patients will receive Metformin 2000mg (oral: 2 tablets1000 mg per day) for months . -after two months from the start: Clomiphene citrate 100mg (2 tablets clomid 50mg each per day, from 2nd to 6th day of the cycle ) will be added every month starting from the 3rd month to the 5th month .
Intervention Type
Drug
Intervention Name(s)
Vit D
Other Intervention Name(s)
Devarol-S
Intervention Description
Injection
Intervention Type
Drug
Intervention Name(s)
Metformin
Other Intervention Name(s)
Glucophage extended release
Intervention Description
tablets
Intervention Type
Drug
Intervention Name(s)
Clomiphene
Other Intervention Name(s)
Clomid
Intervention Description
Tablet
Primary Outcome Measure Information:
Title
Follicle growth and maturation
Description
Transvaginal ultrasound will be done every 48 hours at the start from day 10 of the cycle to assess if the follicle reaches 17-19 mm
Time Frame
11days
Title
Change in Follicle growth and maturation at 3rd month
Description
Transvaginal ultrasound will be done every 48 hours at the start from day 10 of the cycle to assess if the follicle reaches 17-19 mm
Time Frame
11 days
Title
Change in Follicle growth and maturation at 5th month
Description
Transvaginal ultrasound will be done every 48 hours at the start from day 10 of the cycle to assess if the follicle reaches 17-19 mm
Time Frame
11 days
Secondary Outcome Measure Information:
Title
Occurence of Chemical pregnancy occurence
Description
Positive pregnancy test
Time Frame
recorded at any time point during the study whenever occurs up to 5 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of PCOS as defined by the Rotterdam criteria Females age 20-35 years old BMI 18-30 kg/m2 1ry or secondary infertility Clomiphene resistant ( patients didn't - show response: ovulate to dose of 200 mg clomid per day for 3 cycles ) Willingness to comply with study protocol for 5 months Willingness to give written informed consent to participate in the study Exclusion Criteria: Previous metformin intake ovarian drilling tubal factor as evidenced by hysterosalpingogram or laparoscope endometrial pathology ex., polyp Myometrial pathology ex., adenomyosis or fibroid abnormal semen parameters Cushing syndrome Hyperprolactinemia Adrenal secreting tumor
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Reda MK Ghanem, Lecturer
Organizational Affiliation
Obstetrics & Gynecology department Faculty of medicine, Ain shams University.
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Ahmed MN Hashaad, Professor
Organizational Affiliation
Obstetrics & Gynecology department - Faculty of medicine, Ain shams University.
Official's Role
Study Director
Facility Information:
Facility Name
Ain Shams University Maternity hospital
City
Cairo
Country
Egypt

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
De-identified individual participant data for primary and secondary outcome measures will be available
IPD Sharing Time Frame
Within 9 months of study completion
IPD Sharing Access Criteria
Requestors should sign a data access agreement. And requests will be revised

Learn more about this trial

Vitamin D for Polycystic Ovary Syndrome Clomiphene Resistant Women

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