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Effects of Metformin and Oral Hormonal Contraceptive in Adolescents With Polycystic Ovary Syndrome

Primary Purpose

Polycystic Ovary Syndrome

Status
Unknown status
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Placebo
Metformin
Sponsored by
Federal University of São Paulo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Polycystic Ovary Syndrome focused on measuring metformin, Hyperandrogenism, Metabolic Syndrome X, adolescents, melatonin, Polycystic Ovary Syndrome, Insulin Resistance, Menstrual Cycle

Eligibility Criteria

11 Years - 19 Years (Child, Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Patients until 19 years-old, at least 2 years after menarche
  • Patients with Polycystic Ovary Syndrome based on Rotterdan criteries

Exclusion Criteria:

  • Patients with Diabetes Mellitus, hypertension, hyperprolactinemia, adrenal enzymatic deficiency, Cushing syndrome, thyroidopathy, renal or hepatic disfunction
  • Use of OC or insulin-sensitising drugs in the last 90 days before
  • Pregnancy
  • Androgen tumors, hormonal-sensitive tumors in the past
  • Contra-indication to the medications used in the study

Sites / Locations

  • Federal University of Sao PauloRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Metformin

Placebo

Arm Description

Metformin 500mg three times a day for six months

1 capsule three times a day for six months

Outcomes

Primary Outcome Measures

serum melatonin

Secondary Outcome Measures

hormonal and metabolic measurements, clinical assessment

Full Information

First Posted
September 30, 2009
Last Updated
June 24, 2012
Sponsor
Federal University of São Paulo
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1. Study Identification

Unique Protocol Identification Number
NCT00988078
Brief Title
Effects of Metformin and Oral Hormonal Contraceptive in Adolescents With Polycystic Ovary Syndrome
Official Title
Effect of Metformin Therapy on Insulin Resistance and Melatonin in Adolescents With Polycystic Ovary Syndrome.
Study Type
Interventional

2. Study Status

Record Verification Date
October 2009
Overall Recruitment Status
Unknown status
Study Start Date
July 2011 (undefined)
Primary Completion Date
October 2013 (Anticipated)
Study Completion Date
December 2013 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Federal University of São Paulo

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The polycystic ovary syndrome is the most common endocrinopathy in reproductive age women. The pathophysiology of this syndrome remains unclear, but there are evidences that a decreased in insulin sensitivity may be related in this syndrome. There are studies that showed the action of factors on the sensitivity of the insulin receptor, such as melatonin. It is a hormone produced by the pineal gland, whose role is still uncertain in human reproduction, although many studies have found that it may relate sex hormone effect. Many patients with polycystic ovary syndrome (PCOS) may have hyperinsulinemia, and that pinealectomized rats determined hypoglycemia and hyperinsulinemia, with reduced release of insulin in response to glucose. Therefore, it is supposed that blood levels of melatonin might correlate with the blood insulin concentration in patients with the syndrome. Moreover, the insulin sensitizing agents have been used in the treatment of patients with insulin resistance and PCOS, based on its main pathophysiological substrate which is the hyperinsulinemia. In fact, the metformin is the most used in the literature. However, there are few studies on the use of metformin in adolescents. The evidences of this drugs in this group of patients have showed good therapeutic response with few side effects. The objective of the study is to evaluate the effects of metformin on insulin resistance and levels of melatonin in adolescents with PCOS. It will be performed a prospective, randomized, double-blind and placebo-controlled study with 90 adolescents with PCOS. It will be evaluated clinical and laboratory parameters (TSH, free T4, prolactin, FSH, LH, estradiol, total testosterone, androstenedione, DHEA-s, 17-OH progesterone, SHBG, free androgen index, index of HOMA-IR and QUICKI from fasting glucose and insulin, total cholesterol and fractions, triglycerides, creatinine, AST and ALT and creatinkinase, fibrinogen and PAI-1, and melatonin for 6 months of treatment.
Detailed Description
Design: 90 patients will be selected to a prospective, randomized and double-blinded study. They will be assigned to two groups: A) 45 patients, treated with OC (oral contraceptive) and metformin 1500mg/ day. B) 45 patients, treated with OC and placebo. The length of treatment was six months. Inclusion criteria: patients until 19 years-old, at least 2 years after menarche, with Polycystic Ovary Syndrome based on Rotterdan criterion. Exclusion criteria: patients with Diabetes Mellitus, hypertension, hyperprolactinemia, adrenal enzymatic deficiency, Cushing syndrome, thyroidopathy, renal or hepatic disfunction, use of OC or insulin-sensitising drugs in the last 90 days before, pregnancy, androgen tumors, hormonal-sensitive tumors in the past, contra-indication to the medications used in the study. Clinical parameters included are weight and height (for BMI), waist to hip ratio, habits like smoking or drinking, drug addiction, blood pressure measurement, hirsutism and acne. Laboratorial parameters included are TSH, free T4, prolactin, FSH, LH, estradiol, total testosterone, androstenedione, s-DHEA, 17-OH progesterone, SHBG, free androgen index, fasting glucose and insulin, total cholesterol and fractions, triglycerides, creatinin, TGO, TGP, CK, PAI-1, fibrinogen, melatonin. Patients will be evaluated using these parameters in the beginning, 1, 3 and 6 months after use of the drugs.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Polycystic Ovary Syndrome
Keywords
metformin, Hyperandrogenism, Metabolic Syndrome X, adolescents, melatonin, Polycystic Ovary Syndrome, Insulin Resistance, Menstrual Cycle

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Metformin
Arm Type
Experimental
Arm Description
Metformin 500mg three times a day for six months
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
1 capsule three times a day for six months
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Capsule (without biologic action) administered three times a day for six months
Intervention Type
Drug
Intervention Name(s)
Metformin
Intervention Description
Metformin 500mg three times a day for six months
Primary Outcome Measure Information:
Title
serum melatonin
Time Frame
0 and 6 months
Secondary Outcome Measure Information:
Title
hormonal and metabolic measurements, clinical assessment
Time Frame
0, 3 and 6 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
11 Years
Maximum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patients until 19 years-old, at least 2 years after menarche Patients with Polycystic Ovary Syndrome based on Rotterdan criteries Exclusion Criteria: Patients with Diabetes Mellitus, hypertension, hyperprolactinemia, adrenal enzymatic deficiency, Cushing syndrome, thyroidopathy, renal or hepatic disfunction Use of OC or insulin-sensitising drugs in the last 90 days before Pregnancy Androgen tumors, hormonal-sensitive tumors in the past Contra-indication to the medications used in the study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Margareth Iwata
Phone
55-11-24786169
Email
megiwata@yahoo.com
First Name & Middle Initial & Last Name or Official Title & Degree
Valeria Secretaria
Phone
55-11-55793321
Email
valeria.gineco@epm.br
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jose Maria Soares Junior
Organizational Affiliation
Federal University os Sao Paulo
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Alexandre Rossi
Organizational Affiliation
Federal University os Sao Paulo
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Eduardo Leme Alves da Motta
Organizational Affiliation
Federal University os Sao Paulo
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Margareth Chiharu Iwata
Organizational Affiliation
Federal University of Sao Paulo
Official's Role
Principal Investigator
Facility Information:
Facility Name
Federal University of Sao Paulo
City
Sao Paulo
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Margareth Iwata
Email
megiwata@yahoo.com

12. IPD Sharing Statement

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Effects of Metformin and Oral Hormonal Contraceptive in Adolescents With Polycystic Ovary Syndrome

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