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Assessment of effectiveness of oral vitamin D3 on Bacterial vaginosis in women in fertility ages

Phase 2
Conditions
Bacterial vaginosis.
Acute vaginitis
Registration Number
IRCT201105096284N2
Lead Sponsor
Vice chancellor for research, Tehran University of Medical sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
190
Inclusion Criteria

Ages 18-35; Stability in medical condition among 6 months later; Lack of Pathological obesity; Not using tobacco; Lack of history of hypercalcemia, nephrolitiasis or sarcoidosis; Lack of current pregnancy; Lack of recent history of hospitalization; Absence of liver or kidney disorder; current malignancy or malabsorption; Lack of immune suppression, or those drugs that will interfere with vitamin D metabolism, such as phenytoin and carbamazepine; Not taking vitamin D supplements meet; Lack of clinical bacterial vaginosis; Lack of normal amounts of vitamin D in first assessment; Detection of asymptomatic bacterial vaginosis with nugent test

Exclusion criteria: Unwillingness to continue the use of drug; pregnancy occurred; Drug allergy symptoms such as gastrointestinal symptoms; Vaginal infection symptoms like foul-smelling discharge; Use of drug non according to the pharmacist recommendation

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Bacterial vaginosis. Timepoint: 105 days. Method of measurement: Nugent test.
Secondary Outcome Measures
NameTimeMethod
Concentration of vitamin D in serum. Timepoint: 105 days. Method of measurement: Lab test.
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