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Recruiting NCT04355572

Evaluation of the Clinical and Psychological Impact of Vitamin D Replacement in Adolescent Females at Risk for Polycystic Ovarian Syndrome (PCOS)

No phase Interventional Polycystic Ovarian Syndrome in Adolescent Females Vitamin D Deficiency

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Vitamin D 4000IU daily, Placebo.
Who it may be relevant to
Registry conditions: Polycystic Ovarian Syndrome in Adolescent Females, Vitamin D Deficiency. Basic parameters: 13 years — 21 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

This study is a double blind, placebo controlled, randomized trial of study subjects with PCOS and low vitamin D to 2 groups- placebo and vitamin D replacement. Participants and investigators will be blinded to treatment modality until the end of the trial period

Detailed description

Patients referred to the pediatric endocrinology clinic or adolescent gynecology clinic at Yale New Haven Children Hospital with a primary complaint of hirsutism, acne, or amenorrhea and/or oligomenorrhea persisting 2 years after their menarche will be evaluated for polycystic ovarian syndrome through history, physical exam, pelvic ultrasound, and laboratory evaluation, to include androgen testing, thyroid testing, female hormone testing, and diabetic risk testing (this is standard of care). A vitamin D level will also be drawn. While vitamin D level is not currently part of the diagnostic algorithm for PCOS, it is not unreasonable to check in patients in which there is concern for an endocrine disorder. If the patient meets Rotterdam criteria and their serum vitamin D level is between 6 and 29 ng/mL, the patient and their guardian(s) will be approached for inclusion in our study by the physician or dedicated research nursing staff.

If patient and guardian agree to participate and sign a consent / assent form, the patient will then be randomized to receive vitamin D supplement versus placebo and will be followed for 6 months on their randomized replacement with repeat laboratory testing of AMH, vitamin D, lipid profile, glucose and insulin testing, androgen testing, and female hormone testing at the randomization, 3 months and at the end of the course of the trial(6 months). Patients with vitamin D levels 5ng/mL or less will not be randomized, they will be given recommended treatment. Depressive symptoms will be assessed at time of randomization, 3 months post randomization, and 6 months post randomization using the Beck Depression Inventory-II, the gold standard self-report depression inventory. A depression screen is currently administered to all adolescents seen at Yale New Haven Children Hospital outpatient clinics with a protocol for patients who report clinically significant levels of depression. This protocol will remain in place and will not be altered during this research study.

After post-trial testing, patients will be unblinded and patients who still have vitamin D below threshold will be offered vitamin D treatment.

Aim 1: To investigate the effect of vitamin D replacement upon biochemical parameters of polycystic ovarian syndrome (PCOS) in adolescent female patients. Hypothesis: Replacement of vitamin D to normal levels in adolescents with PCOS and/or at risk for PCOS and low levels of vitamin D will lower serum androgen and anti-mullerian hormone (AMH) levels.

Aim 2: To investigate the effect of vitamin D replacement on clinical features of PCOS in adolescent female patients. Hypothesis: Replacement of vitamin D in adolescents with PCOS and/or at risk for PCOS and low levels of vitamin D will improve symptoms of menstrual irregularities, acne, and hirsutism.

Aim3: To investigate the effect of vitamin D replacement on depressive symptoms in adolescent female patients with PCOS. Hypothesis: Replacement of vitamin D in adolescents with PCOS or at risk for PCOS and low levels of serum vitamin D will improve symptoms of depression.

Interventions

  • Drug Vitamin D 4000IU daily
    Randomized to receive vitamin D 4000IU daily
  • Drug Placebo
    Randomized to placebo daily

Primary outcome measures

  • Change in oligomenorrhea [Time frame: 6 months]
  • Changes Vitamin D (25-hydroxyvitamin D) level [Time frame: at enrollment, at 3 months after randomization and 6 months after randomization]
Secondary outcome measures (7)
  • Change in DHEAS level [Time frame: at enrollment, at 3 months after randomization and 6 months after randomization]
  • Changes in Androstenedione level [Time frame: at enrollment, at 3 months after randomization and 6 months after randomization]
  • Change in Anti-Mullerian hormone (AMH) level [Time frame: at enrollment, at 3 months after randomization and 6 months after randomization]
  • Change in testosterone level [Time frame: at enrollment, at 3 months after randomization and 6 months after randomization]
  • Change in Hirsutism [Time frame: at enrollment, at 3 months after randomization and 6 months after randomization]
  • Change Body Acne [Time frame: at enrollment, at 3 months after randomization and 6 months after randomization]
  • Change in Facial [Time frame: at enrollment, at 3 months after randomization and 6 months after randomization]

Eligibility criteria

Inclusion criteria

\- Postmenarchal adolescent females aged 13-21 who meet modified Rotterdam criteria for PCOS, with a serum vitamin D level between 6-29 ng/mL.

Exclusion criteria

  • Other causes for hyperandrogenism,
  • Chronic renal diseases,
  • Acquired or inherited calcium and vitamin D metabolic disorders.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Treatment

Study locations

United States · 1 center
  • Yale New Haven Children's Hospital — New Haven

Identifiers

NCT: NCT04355572 · 2000028054 · 000

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗