Actively Recruiting
Efficacy of Injectable Vitamin D Supplementation in Females With Polycystic Ovary Syndrome
Led by Aga Khan University · Updated on 2025-02-18
142
Participants Needed
1
Research Sites
156 weeks
Total Duration
On this page
Sponsors
A
Aga Khan University
Lead Sponsor
P
Pakistan Science Foundation
Collaborating Sponsor
AI-Summary
What this Trial Is About
Poly cystic Ovarian Syndrome (PCOS) is an endocrine disorder of reproductive age defined by "the presence of any two out of three criteria: oligo and/or anovulation, excess androgen activity and/or polycystic ovarian morphology on ultrasound". Considering role of vitamin D (VD) (3, 4) and high prevalence (58%) of deficiency in PCOS of Pakistan. Researchers hypothesized that its correction would improve response to standard PCOS treatment. The objective is to compare PCOS parameters in intervention group (Group A) receiving VD supplementation and then PCOS care with control group (Group B) receiving standard PCOS care and then VD supplementation. A randomized open label trial: delayed-start design will be conducted on VD deficient PCOS females VD \< 20ng/ml ; Group A will receive VD injections 600,000 I.U I/M once with 1 gram calcium supplement daily in the initial 12 weeks. After that standard PCOS care; i) Glucophage XR 750 mg (once for 15 days then twice daily) ii) progesterone supplementation (1 capsule Progeffik 100 mg every 3 weeks, then 1 week off) and iii) calcium supplements will be given for next 12 weeks. PCOS females in Group B will receive standard PCOS care (same) with addition of VD and calcium supplementation after 12 weeks till study end point. Study outcomes will be comparison of i) hyperandrogenism by Free Androgen Index \[Total Testosterone, Steroid Hormone Binding Globulin ii) insulin Resistance by HOMA-IR (serum Insulin, Fasting Blood Glucose) and iii) oxidative stress by Total Antioxidant Capacity after 24-weeks in these Groups'd levels after supplementation will be assessed for confirmation of correction and calcium and albumin levels for detection of hypercalcemia. Results of this study will inform the clinicians to add VD before or after the standard PCOS care for rectification of endocrine and metabolic derangements as a cost-effective treatment and prevention strategy in these females.
CONDITIONS
Official Title
Efficacy of Injectable Vitamin D Supplementation in Females With Polycystic Ovary Syndrome
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Females aged 18 to 45 years
- Recently diagnosed with PCOS showing at least two of the following: clinical or biochemical hyperandrogenism, chronic anovulation, or polycystic ovaries on ultrasound
- Vitamin D deficiency with serum levels below 20 ng/ml
- Any ethnic background
You will not qualify if you...
- Pregnancy
- Hypercalcemia with plasma calcium over 2.65 mmol/L
- Tuberculosis or other granulomatous diseases
- Chronic liver disease or alanine transaminase (ALT) levels three times above normal
- Chronic kidney disease or serum creatinine above 2.0 mg/dL
- Recent vitamin D injection in the last 3 months
- Use of oral contraceptives, hormonal replacement, glucocorticoids, calcium supplements, insulin-sensitizing drugs, lipid-lowering drugs, or other medications affecting insulin or androgens within 3 months
- Conditions like congenital adrenal hyperplasia, Cushing's syndrome, androgen-secreting tumors, type 2 diabetes, renal, hepatic, thyroid disorders, hyperparathyroidism, malabsorption syndromes, cystic fibrosis
- Unexplained vaginal bleeding
- COVID-19 infection within the last 3 months
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Trial Site Locations
Total: 1 location
1
Aga Khan University Hospital
Karachi, Sindh, Pakistan, 75500
Actively Recruiting
Research Team
R
Rehana Rehman, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
TREATMENT
Number of Arms
2
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