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Therapeutic Monitoring of Metformin in Women With Polycystic Ovary Syndrome

Primary Purpose

Polycystic Ovary Syndrome

Status
Unknown status
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
Metformin
Sponsored by
Biocinese
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Polycystic Ovary Syndrome focused on measuring polycystic ovary syndrome, metformin, pharmacokinetic

Eligibility Criteria

18 Years - 40 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients aged between 18 and 40 years old, with no use of contraceptive drugs or insulin sensitizing agents for more than 3 months.
  • PCOS diagnosis.
  • Insulin resistance Index by the Homeostatic model Assessment Formula higher than 2.5.

Exclusion Criteria:

  • Another diseases with androgen excess;
  • Patients with history of serious adverse reaction or hypersensibility to any medicine;
  • History or presence of renal, hepatic or gastrointestinal disorders.
  • Continuous use of any pharmaco, inclusively metformin

Sites / Locations

  • BiocineseRecruiting

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Metformin

Arm Description

study parallel with one arm only.

Outcomes

Primary Outcome Measures

Plasma concentration of metformin
Blood samples are collected from each patient and the plasma concentration is analysed.

Secondary Outcome Measures

Number of adverse events
All adverse events are registered during the treatment

Full Information

First Posted
June 2, 2011
Last Updated
June 3, 2011
Sponsor
Biocinese
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1. Study Identification

Unique Protocol Identification Number
NCT01366391
Brief Title
Therapeutic Monitoring of Metformin in Women With Polycystic Ovary Syndrome
Official Title
Therapeutic Monitoring of Metformin in Women With Polycystic Ovary Syndrome
Study Type
Interventional

2. Study Status

Record Verification Date
June 2011
Overall Recruitment Status
Unknown status
Study Start Date
January 2011 (undefined)
Primary Completion Date
August 2011 (Anticipated)
Study Completion Date
October 2011 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Biocinese

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Metformin is one of the most commonly prescribed drugs worldwide for the treatment of Type 2 Diabetes. It has been currently used for the treatment of: polycystic ovary syndrome, gestational diabetes, metabolic syndrome and obesity. In patients with polycystic ovary syndrome (PCOS) the adverse side effects are a frequent cause for treatment discontinuation. In every day medical practice lower doses of Metformin are administered searching for the continuation of the treatment. However, there is no clinical study to support this assertion. The objective of this study is to monitor and correlate the therapeutic effect of Metformin on patients with PCOS taking daily doses of 1500mg and 1000mg.
Detailed Description
Patients with PCOS diagnosis and that are able to attempt the inclusion criteria are divided in two groups: administration of metformin 500 mg tablet three times/day as well 1500 mg/day (group A)and administration of metformin 500 mg tablet twice/day or 1000 mg/day (group B). Blood samples were collected to the pharmacokinetic evaluation from first day of administration until 3 months after beginning of treatment. The patients are monitored during 3 months and all side effects are register. The efficacy of both treatment are analyzed by biochemical and physical evaluation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Polycystic Ovary Syndrome
Keywords
polycystic ovary syndrome, metformin, pharmacokinetic

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Metformin
Arm Type
Other
Arm Description
study parallel with one arm only.
Intervention Type
Drug
Intervention Name(s)
Metformin
Other Intervention Name(s)
Glifage 500 mg
Intervention Description
Metformin 500 mg tablet (1000 or 1500 mg/day)
Primary Outcome Measure Information:
Title
Plasma concentration of metformin
Description
Blood samples are collected from each patient and the plasma concentration is analysed.
Time Frame
First day after administration until 3 months after begining of treatment
Secondary Outcome Measure Information:
Title
Number of adverse events
Description
All adverse events are registered during the treatment
Time Frame
observation during 3 months of treatment

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients aged between 18 and 40 years old, with no use of contraceptive drugs or insulin sensitizing agents for more than 3 months. PCOS diagnosis. Insulin resistance Index by the Homeostatic model Assessment Formula higher than 2.5. Exclusion Criteria: Another diseases with androgen excess; Patients with history of serious adverse reaction or hypersensibility to any medicine; History or presence of renal, hepatic or gastrointestinal disorders. Continuous use of any pharmaco, inclusively metformin
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Naura Angonese, Dr
Phone
+55 45 2103 1900
Email
naura.tonin@hotmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Josélia Manfio, Dr
Phone
+55 45 21031907
Email
manfiojoselia@bol.com.br
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Naura Angonese, Dr
Organizational Affiliation
Biocinese
Official's Role
Principal Investigator
Facility Information:
Facility Name
Biocinese
City
Toledo
State/Province
Parana
ZIP/Postal Code
85903-590
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Joselia Manfio, Dr
Phone
+55 45 2103 1907
Email
manfiojoselia@bol.com.br
First Name & Middle Initial & Last Name & Degree
Naura Angonese, Dr
Phone
+55 45 2103 1900
Email
naura.tonin@hotmail.com
First Name & Middle Initial & Last Name & Degree
Naura Angonese, Dr

12. IPD Sharing Statement

Learn more about this trial

Therapeutic Monitoring of Metformin in Women With Polycystic Ovary Syndrome

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