Spironolactone Plus Metformin in Polycystic Ovary Syndrome
Primary Purpose
Polycystic Ovary Syndrome
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Metformin
Metformin plus Spironolactone
Sponsored by
About this trial
This is an interventional treatment trial for Polycystic Ovary Syndrome focused on measuring PCOS, metformin, spironolactone, metabolic syndrome, hyperandrogenism
Eligibility Criteria
Inclusion Criteria:
- Overweight/obese patients with PCOS
Exclusion Criteria:
- Other causes of hyperandrogenism and
Use of drugs including:
- oral contraceptive
- anti-hypertensive agents
- anti-diabetic drugs
- agents for weight loss
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Metformin
Metformin plus spironolactone
Arm Description
850 mg/day twice a day
Metformin 850 mg twice a day for six months plus Spironolactone 25 mg day
Outcomes
Primary Outcome Measures
Metformin versus Metformin plus low-dose Spironolactone on metabolic parameters of Patients with Polycystic Ovary Syndrome: a randomized study
We evaluated metabolic parameters across anthropometric parameters: height, weight, waist circumference, BMI, glycemia, lipid profile, blood count, coagulation parameters, hepatic and renal function indexes, OGTT and HOMA-IR. The diagnosis of MetS was established according to the ATPIII criteria
Secondary Outcome Measures
Spironolactone versus Metformin plus spironolactone in hyperandrogenism in Polycystic Ovary Syndrome
We evaluated hyperandrogenism across Hirsutism Score, measuring total testosterone, SHBG, Δ4androstenedione, DHEA-S and FAI. All patients underwent ovarian ultrasound examination.
Full Information
NCT ID
NCT01526616
First Posted
January 27, 2012
Last Updated
February 3, 2012
Sponsor
University Magna Graecia
1. Study Identification
Unique Protocol Identification Number
NCT01526616
Brief Title
Spironolactone Plus Metformin in Polycystic Ovary Syndrome
Official Title
Metformin Versus Metfotmin Plus Low-dose Spironolactone in the Treatment of Overweight/Obese Patients With Polycystic Ovary Syndrome: a Randomized Study
Study Type
Interventional
2. Study Status
Record Verification Date
February 2012
Overall Recruitment Status
Completed
Study Start Date
May 2010 (undefined)
Primary Completion Date
May 2011 (Actual)
Study Completion Date
July 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Magna Graecia
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The investigators examined whether a combined therapy with low-dose spironolactone plus metformin is more effective than metformin alone in 52 overweight/obese Polycystic Ovary Syndrome (PCOS) patients.
Detailed Description
In the present prospective, randomized study, we evaluated the efficacy of a combined therapy with metformin and low-dose spironolactone as compared to metformin alone on the clinical and endocrine-metabolic alterations of PCOS patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Polycystic Ovary Syndrome
Keywords
PCOS, metformin, spironolactone, metabolic syndrome, hyperandrogenism
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
56 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Metformin
Arm Type
Active Comparator
Arm Description
850 mg/day twice a day
Arm Title
Metformin plus spironolactone
Arm Type
Active Comparator
Arm Description
Metformin 850 mg twice a day for six months plus Spironolactone 25 mg day
Intervention Type
Drug
Intervention Name(s)
Metformin
Intervention Description
Metformin 850 mg twice a day for six months
Intervention Type
Drug
Intervention Name(s)
Metformin plus Spironolactone
Intervention Description
Metformin 850 mg twice a day for six months plus Spironolactone 25 mg day
Primary Outcome Measure Information:
Title
Metformin versus Metformin plus low-dose Spironolactone on metabolic parameters of Patients with Polycystic Ovary Syndrome: a randomized study
Description
We evaluated metabolic parameters across anthropometric parameters: height, weight, waist circumference, BMI, glycemia, lipid profile, blood count, coagulation parameters, hepatic and renal function indexes, OGTT and HOMA-IR. The diagnosis of MetS was established according to the ATPIII criteria
Time Frame
six months
Secondary Outcome Measure Information:
Title
Spironolactone versus Metformin plus spironolactone in hyperandrogenism in Polycystic Ovary Syndrome
Description
We evaluated hyperandrogenism across Hirsutism Score, measuring total testosterone, SHBG, Δ4androstenedione, DHEA-S and FAI. All patients underwent ovarian ultrasound examination.
Time Frame
six months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Overweight/obese patients with PCOS
Exclusion Criteria:
Other causes of hyperandrogenism and
Use of drugs including:
oral contraceptive
anti-hypertensive agents
anti-diabetic drugs
agents for weight loss
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
A. Mazza B. Fruci A. Belfiore, Doctors
Organizational Affiliation
Endocrinology Unit
Official's Role
Principal Investigator
12. IPD Sharing Statement
Citations:
PubMed Identifier
23845740
Citation
Mazza A, Fruci B, Guzzi P, D'Orrico B, Malaguarnera R, Veltri P, Fava A, Belfiore A. In PCOS patients the addition of low-dose spironolactone induces a more marked reduction of clinical and biochemical hyperandrogenism than metformin alone. Nutr Metab Cardiovasc Dis. 2014 Feb;24(2):132-9. doi: 10.1016/j.numecd.2013.04.016. Epub 2013 Jul 8.
Results Reference
derived
Learn more about this trial
Spironolactone Plus Metformin in Polycystic Ovary Syndrome
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