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Effects of Cyproterone Compound-spironolactone, Metformin and Pioglitazone on Inflammatory Markers in PCOS (AntiPCO)

Primary Purpose

Polycystic Ovary Syndrome

Status
Completed
Phase
Early Phase 1
Locations
Iran, Islamic Republic of
Study Type
Interventional
Intervention
Cyproterone compound + Spironolactone
Metformin
Pioglitazone
Sponsored by
Shiraz University of Medical Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Polycystic Ovary Syndrome focused on measuring Inflammation, Complement system proteins, Homocysteine, C-Reactive Protein, Cyproterone, Ethinyl Estradiol, Androgen Antagonists, Metformin, Thiazolidinediones, Pioglitazone

Eligibility Criteria

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

Inclusion Criteria:

  • Age 18-35 years
  • Diagnosis of Polycystic Ovary Syndrome (PCOS) according to Rotterdam criteria 2003 (two out of three required):

    1. Oligomenorrhea or anovulation
    2. Clinical and/or biochemical signs of hyperandrogenism
    3. Polycystic ovaries (by ultrasound)

Exclusion Criteria:

  • Smoking
  • Pregnancy
  • Diabetes mellitus
  • Renal failure (serum creatinine >1.5)
  • Congenital adrenal hyperplasia
  • Hyper or hypothyroidism
  • Sex hormone therapy or antiandrogen therapy during the last three months
  • Unexplained serum alanin aminotransferase (ALT) elevation more than 2.5 times above normal range
  • Any systemic or febrile illnesses
  • Use of glucocorticoid or anti-inflammatory drugs during the last three months
  • Androgen secreting tumor
  • Malignancy

Sites / Locations

  • Shahid Motahhari Clinic, Shiraz University of Medical Sciences

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

Cyproterone compound + Spironolactone

Metformin

Pioglitazone

Arm Description

Cyproterone compound (Cyproterone acetate 2mg+Ethinyl estradiol 35 mcg) once daily + Spironolactone 50 mg twice daily

Metformin 1500 mg daily

Pioglitazone 30 mg daily

Outcomes

Primary Outcome Measures

Serum C3 level
Serum concentration of a component of complement cascade: C3
Serum C4 level
Serum concentration of a component of complement cascade: C4
Serum high-sensitive CRP (C-reactive protein)
Serum concentration of high-sensitive C-reactive protein (hs-CRP)

Secondary Outcome Measures

Serum total Testosterone level
Serum concentration of total Testosterone
Serum free Testosterone level
Serum concentration of free Testosterone
Serum Dehydroepiandrosterone sulfate (DHEAS) level
Serum concentration of Dehydroepiandrosterone sulfate
Serum follicle stimulating hormone (FSH) level
Serum concentration of follicle stimulating hormone
Serum luteinizing hormone (LH) level
Serum concentration of luteinizing hormone
Fasting Blood Sugar (FBS)
Fasting Blood Sugar
Fasting Serum Insulin level
Serum concentration of insulin
Serum homocysteine level
Serum concentration of homocysteine
Number of patients with adverse events
Number of patients with adverse events

Full Information

First Posted
February 19, 2016
Last Updated
November 8, 2019
Sponsor
Shiraz University of Medical Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT02689843
Brief Title
Effects of Cyproterone Compound-spironolactone, Metformin and Pioglitazone on Inflammatory Markers in PCOS
Acronym
AntiPCO
Official Title
Effects of Treatment With Cyproterone Compound-spironolactone, Metformin and Pioglitazone on Serum Inflammatory Markers in Patients With Polycystic Ovary Syndrome (PCOS)
Study Type
Interventional

2. Study Status

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

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shiraz University of Medical Sciences

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
The aim of this study is to evaluate the effects of three-month course of treatment modalities (Cyproterone compound-Spironolactone, Metformin and Pioglitazone) in patients with polycystic ovary syndrome (PCOS) on markers of inflammation [serum complement, homocysteine and high sensitive C-reactive protein (hs-CRP)] levels.
Detailed Description
Polycystic ovary syndrome (PCOS) is estimated to affect up to10% of women of reproductive age, making it one of the most common endocrine disorders in this population. PCOS is associated with a broad range of adverse sequel, including hypertension, dyslipidemia, insulin resistance, hyperandrogenaemia, gestational and type 2 diabetes,which ultimately increase the cardiovascular morbidity in these patients. Also PCOS is increasingly recognized as a component of the metabolic syndrome. Management depends on symptoms or the source of androgen excess. Several treatment options are available, which allows for an individualized approach. Spironolactone is the safest potent available antiandrogen. It is effective in lowering the hirsutism score by approximately one third, although considerable individual variations exist. Other antiandrogens used to treat hirsutism and hirsutism equivalents include cyproterone acetate that has weak antiglucocorticoid effects. Metformin and thiazolidinediones, are promising adjuncts for treating PCOS. Although both of them increase insulin sensitivity, but their mechanism of action differ. Serum complement, homocysteine and C-reactive protein (CRP) levels have been reported to be linked with insulin resistance. The investigators want to measure serum complement, homocysteine and hs-CRP levels in patients with PCOS before and after three-month course of treatment with Cyproterone compound-Spironolactone (CC-S), metformin (M) and pioglitazone (P).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Polycystic Ovary Syndrome
Keywords
Inflammation, Complement system proteins, Homocysteine, C-Reactive Protein, Cyproterone, Ethinyl Estradiol, Androgen Antagonists, Metformin, Thiazolidinediones, Pioglitazone

7. Study Design

Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
90 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Cyproterone compound + Spironolactone
Arm Type
Active Comparator
Arm Description
Cyproterone compound (Cyproterone acetate 2mg+Ethinyl estradiol 35 mcg) once daily + Spironolactone 50 mg twice daily
Arm Title
Metformin
Arm Type
Active Comparator
Arm Description
Metformin 1500 mg daily
Arm Title
Pioglitazone
Arm Type
Active Comparator
Arm Description
Pioglitazone 30 mg daily
Intervention Type
Drug
Intervention Name(s)
Cyproterone compound + Spironolactone
Other Intervention Name(s)
CC-S
Intervention Description
Cyproterone compound (Cyproterone Acetate 2mg-Ethinyl estradiol 35mcg) 1 tablet daily + Spironolactone 50 mg twice daily
Intervention Type
Drug
Intervention Name(s)
Metformin
Intervention Description
Metformin 500mg three times daily
Intervention Type
Drug
Intervention Name(s)
Pioglitazone
Intervention Description
Pioglitazone 30mg once daily
Primary Outcome Measure Information:
Title
Serum C3 level
Description
Serum concentration of a component of complement cascade: C3
Time Frame
3 months
Title
Serum C4 level
Description
Serum concentration of a component of complement cascade: C4
Time Frame
3 months
Title
Serum high-sensitive CRP (C-reactive protein)
Description
Serum concentration of high-sensitive C-reactive protein (hs-CRP)
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Serum total Testosterone level
Description
Serum concentration of total Testosterone
Time Frame
3 months
Title
Serum free Testosterone level
Description
Serum concentration of free Testosterone
Time Frame
3 months
Title
Serum Dehydroepiandrosterone sulfate (DHEAS) level
Description
Serum concentration of Dehydroepiandrosterone sulfate
Time Frame
3 months
Title
Serum follicle stimulating hormone (FSH) level
Description
Serum concentration of follicle stimulating hormone
Time Frame
3 months
Title
Serum luteinizing hormone (LH) level
Description
Serum concentration of luteinizing hormone
Time Frame
3 months
Title
Fasting Blood Sugar (FBS)
Description
Fasting Blood Sugar
Time Frame
3 months
Title
Fasting Serum Insulin level
Description
Serum concentration of insulin
Time Frame
3 months
Title
Serum homocysteine level
Description
Serum concentration of homocysteine
Time Frame
3 months
Title
Number of patients with adverse events
Description
Number of patients with adverse events
Time Frame
3 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18-35 years Diagnosis of Polycystic Ovary Syndrome (PCOS) according to Rotterdam criteria 2003 (two out of three required): Oligomenorrhea or anovulation Clinical and/or biochemical signs of hyperandrogenism Polycystic ovaries (by ultrasound) Exclusion Criteria: Smoking Pregnancy Diabetes mellitus Renal failure (serum creatinine >1.5) Congenital adrenal hyperplasia Hyper or hypothyroidism Sex hormone therapy or antiandrogen therapy during the last three months Unexplained serum alanin aminotransferase (ALT) elevation more than 2.5 times above normal range Any systemic or febrile illnesses Use of glucocorticoid or anti-inflammatory drugs during the last three months Androgen secreting tumor Malignancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mesbah Shams, MD
Organizational Affiliation
Endocrine and Metabolism Research Center, Shiraz University of Medical Sciences
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Gholamhossein R Omrani, MD
Organizational Affiliation
Endocrine and Metabolism Research Center, Shiraz University of Medical Sciences
Official's Role
Study Chair
Facility Information:
Facility Name
Shahid Motahhari Clinic, Shiraz University of Medical Sciences
City
Shiraz
State/Province
Fars
Country
Iran, Islamic Republic of

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Effects of Cyproterone Compound-spironolactone, Metformin and Pioglitazone on Inflammatory Markers in PCOS

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