Skip to content

The effect of vitamin D on the treatment of prostate hypertrophy

The effect of vitamin D supplements on benign hypertrophy

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180922041089N3
Enrollment
54
Registered
2019-09-03
Start date
2018-11-22
Completion date
Unknown
Last updated
2020-09-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Benign prostatic hypertrophy. Benign Prostatic Hypertrophy

Interventions

Intervention 1: Intervention group: The intervention group includes people 50 years old and older who receive pills Vitamin D with a dose of 50000 for 6 months.This drug should be taken every two week

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
50 Years to No maximum

Inclusion criteria

Inclusion criteria: Man over 50 years old Asymptomatic or mild symptoms of benign prostatic hypertrophy based on the IPSS questionnaire. Patients with benign prostatic hypertrophy

Exclusion criteria

Exclusion criteria: BMI greater than 35 or pathologic weight loss (weight loss over 10% of body weight in the last 6 months) History of kidney stones, bladder and urinary tract Having prostate or bladder cancer or prostate surgery Acute or chronic prostatitis or frequent urinary tract infections• History of acute urinary retention or repeated catheters in the last three months Use of GnRH agonists, anti-androgens and any hormonal drug in the past six months, the use of herbal and non-herbal medicines to control and treat BPH The history of chronic diseases such as CVA, HTN, COPD, liver and kidney disease, and cancers .. Taking medications that affect vitamin D metabolism such as corticosteroids, phenytoin, phenobarbital, or regular use of vitamin D supplements over the past 3 months Taking diuretics such as Lasix and ... Alcohol consumption

Design outcomes

Primary

MeasureTime frame
Prostate Volume. Timepoint: At the beginning of the study and six months later. Method of measurement: sonography.

Secondary

MeasureTime frame
Severity of clinical symptoms. Timepoint: At the beginning of the study, 3 months later, 6 months later. Method of measurement: IPSS questionnaire.;PSA. Timepoint: At the beginning of the study, 3 months later, 6 months later. Method of measurement: laboratory kit.;Vitamin D. Timepoint: At the beginning of the study, 3 months later, 6 months later. Method of measurement: blood test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAbolfazl Zendedel

Tehran University of Medical Sciences

azendedel@sina.tums.ac.ir+98 21 5517 6031

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026