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Metformin Treatment in Adolescent Patients With PCOS: A Long-term, Winning Metabolic Choice.

Primary Purpose

Polycystic Ovary Syndrome

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Metformin
Sponsored by
University of Cagliari
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Polycystic Ovary Syndrome focused on measuring insulin resistance, metformin, adolescents

Eligibility Criteria

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

Inclusion Criteria: Pcos Adolescents - Exclusion Criteria: Other type of hyperandrogenism

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    Metformin group

    Control group

    Arm Description

    Treated with metformin

    not treated

    Outcomes

    Primary Outcome Measures

    Insulin resistance change in eighty hyperinsulinemic patients after metformin therapy and its discontinuation
    To verify metformin treatment's immediate and long-term efficacy in hyperinsulinemic adolescent patients with PCOS and the evolution of metabolic status after treatment discontinuation.
    Androgen levels change in eighty hyperinsulinemic patients after metformin therapy and its discontinuation
    To compare changes in androgen plasmatic levels such as total testosterone (TT) and delta-4-androstenedione (A) between the hyperinsulinemic adolescent patients with PCOS and the control group who have not received the metformin treatment by immediate and secondary assessment at the end of treatment of androgen plasmatic levels.

    Secondary Outcome Measures

    Full Information

    First Posted
    August 3, 2023
    Last Updated
    August 22, 2023
    Sponsor
    University of Cagliari
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    1. Study Identification

    Unique Protocol Identification Number
    NCT06015594
    Brief Title
    Metformin Treatment in Adolescent Patients With PCOS: A Long-term, Winning Metabolic Choice.
    Official Title
    Metformin Treatment in Adolescent Patients With PCOS: A Long-term, Winning Metabolic Choice. Results From a Single Center 5-years Retrospective Clinical Study
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2023
    Overall Recruitment Status
    Completed
    Study Start Date
    January 1, 2015 (Actual)
    Primary Completion Date
    August 1, 2019 (Actual)
    Study Completion Date
    May 1, 2022 (Actual)

    3. Sponsor/Collaborators

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

    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 aimed to understand whether metformin therapy can improve insulin resistance in adolescent PCOS patients, both during treatment and after discontinuation, and to evaluate its action on the hormonal and metabolic pathways.
    Detailed Description
    Data were retrospectively retrieved from a database of clinical data collected in the Outpatient Pediatric and Adolescent Gynecology Clinic of the University Hospital "Duilio Casula," Monserrato, Cagliari (Division of Gynecology and Obstetrics, Department of Surgical Sciences, University of Cagliari, Italy), between 2015 and 2019. PCOS diagnosis was adapted for age following the 2019 update from Witchel SF and Carmina's recommendation. The population consisted of 168 PCOS patients aged 12 to 17. Clinical examination, medical history, blood sampling, and pelvic ultrasound (US) were performed. The number of post-menarche years and the body mass index (BMI) were collected. The patients were subjected to physical examination to evaluate hirsutism, according to the criteria of the Ferriman and Gallwey score, as well as acne, using the Cremoncini classification. Each participant received detailed advice on improving their lifestyle, such as physical activity and nutrition. Investigators gave indications of the various food and their weighted intake and a balanced composition of macronutrients (carbohydrates 55%, lipids 25%, protein 20%; fiber ≥25 g/day), as recommended by the Reference intake levels of nutrients and energy for the Italian population (LARN) guidelines. Vegetables, fruit, cereals, fish, and pulses, typical of the Mediterranean style, were included in the diet. Investigators recommended ≥150 minutes per week of moderate or ≥75 minutes of vigorous-intensity exercise for weight gain prevention, minimizing sedentary time, and including strength training exercises for two days per week, as reported from the 2018 PCOS guideline. Laboratory evaluations were performed during the menstrual cycle's first follicular phase (days 3-7) and after a fast of 10-12 hours. Menstrual bleeding was induced by administering medroxyprogesterone acetate (10 mg/day for five days) in amenorrhoeic patients. Follicle-stimulating hormone (FSH), luteinizing hormone (LH), 17-β estradiol (E2), total testosterone (TT), delta-4-androstenedione (A), 17-hydroxyprogesterone (17-OH-P) and sex hormone binding globulin (SHBG) were tested. In addition, total cholesterol, HDL, LDL, and triglycerides were measured with these blood tests. The following day, the patients underwent a 75 g oral glucose tolerance test (OGTT). The OGTT was performed at 9 am after fasting overnight. Blood samples were collected basally and 60, 90, 120, and 180 min after ingesting 75 g of glucose in 150 ml of water. Insulin and glucose were assayed in all samples. Serum E2, FSH, LH, and TT were measured by chemiluminescence immunoassay Immulite (Siemens Products Corporation, Los Angeles, CA). Enzymatic methods were used for glucose, cholesterol, and triglycerides determination. Radioimmunoassay (RIA) was used to measure serum A, insulin and 17-OHP (Diagnostic System Laboratories, Inc. [DSL], Webster, TX). Insulin and glucose values were expressed as the area under the curve (AUC). The AUC was calculated using the trapezoidal rule method and reported as mIU/ml times 180 min for insulin. A normal glycemic response to OGTT was defined according to the criteria of the National Diabetes Data Group (1979). As previously described, a normal insulinemic response to OGTT was defined by a threshold AUC value of 16,900 mIU / ml / 180 min. Insulin sensitivity evaluation was estimated using the homeostatic model assessment index (HOMA), which was calculated as follows: HOMA = [fasting insulin (mU/ml) * fasting glucose (mmol/l)/22, 5]. The same operator acquired ovarian morphology and ovarian volume for all patients. Ultrasound was performed by a transabdominal probe in a whole bladder or transvaginally. A Voluson E6 ultrasound system equipped with a 2-8 MHz RAB4-8-D convex transducer (GE Medical Systems, Austria) was used for the investigation. The ultrasound examination was performed on the same day the blood samples were taken. Ovarian volume was calculated using the formula for a modified prolate ellipsoid (longitudinal x transverse x anterior-posterior * 0.5233). The mean volume values of both ovaries were included in the statistical analysis. Participants were categorized into two groups: the study group, consisting of patients who received metformin therapy, and the control group, which did not receive metformin during the study period. The metformin dose was determined based on the study by Fulghesu et al. Both the study and control group underwent the same combined oral contraceptive pills (COCs), containing drospirenone 3 mg/ethinyl estradiol 20 μg (3 mg DRSP/20 μg EE-24/4). Follow-up was performed every 3-6 months in the first year, then after 12 months by OGTT and clinical evaluation. After about 24 months of treatment, the patients returned to the hospital and repeated clinical and laboratory examinations. Finally, the patients repeated the same blood tests and overall assessment at least 24 months after discontinuing metformin therapy. Baseline data are expressed as b-AUC, b-HOMA, and b-BMI. End-of-therapy evaluation data are described as e-AUC, e-HOMA, and e-BMI. Evaluation data after the end of therapy are reported as ae-AUC, ae-HOMA, and ae-BMI. Patient data were collected anonymously on an Excel® database (Office 365). Statistical analysis was performed using the IBM SPSS Statistics statistical software, version 26 (IBM SPSS Statistics, Chicago, IL, USA). Measurement data corresponding to the normal distribution were expressed by mean ± SD, and the t-test was used for the paired samples (Student's t-test). In addition, the count data were expressed as n (%), and the beta coefficient of linear regression with a 95% confidence interval (95% CI) was reported for each analysis. In all calculations, a p-value < 0.05 was considered significant.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Polycystic Ovary Syndrome
    Keywords
    insulin resistance, metformin, adolescents

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Participant
    Allocation
    Non-Randomized
    Enrollment
    168 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Metformin group
    Arm Type
    Experimental
    Arm Description
    Treated with metformin
    Arm Title
    Control group
    Arm Type
    No Intervention
    Arm Description
    not treated
    Intervention Type
    Drug
    Intervention Name(s)
    Metformin
    Intervention Description
    Patients treated with metformin
    Primary Outcome Measure Information:
    Title
    Insulin resistance change in eighty hyperinsulinemic patients after metformin therapy and its discontinuation
    Description
    To verify metformin treatment's immediate and long-term efficacy in hyperinsulinemic adolescent patients with PCOS and the evolution of metabolic status after treatment discontinuation.
    Time Frame
    about 3 years
    Title
    Androgen levels change in eighty hyperinsulinemic patients after metformin therapy and its discontinuation
    Description
    To compare changes in androgen plasmatic levels such as total testosterone (TT) and delta-4-androstenedione (A) between the hyperinsulinemic adolescent patients with PCOS and the control group who have not received the metformin treatment by immediate and secondary assessment at the end of treatment of androgen plasmatic levels.
    Time Frame
    about 3 years

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    10 Years
    Maximum Age & Unit of Time
    19 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Pcos Adolescents - Exclusion Criteria: Other type of hyperandrogenism

    12. IPD Sharing Statement

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    Metformin Treatment in Adolescent Patients With PCOS: A Long-term, Winning Metabolic Choice.

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