BPH Clinical Trial
Official title:
EFFICACY EVALUATION OF PRUNUS DOMESTICA EXTRACT ON BENIGN PROSTATE HYPERPLASIA (BPH): An Add on Study
Verified date | May 2016 |
Source | Chemical Resources |
Contact | n/a |
Is FDA regulated | No |
Health authority | India: Food Safety And Standards Authority of India |
Study type | Interventional |
Benign prostatic hyperplasia (BPH) is a nonmalignant enlargement of the prostate Prunus
domestica bark contains three groups of active constituents: phytosterols (including
beta-sitosterol), pentacyclic triterpenoids (including ursolic and oleaic acids) and ferulic
esters of long-chain fatty alcohols (including ferulic esters of docosanol and
tetracosanol).
The phytosterols, particularly beta-sitosterol, are found in numerous plants and are
anti-inflammatory, inhibiting the synthesis of prostaglandins. Beta-sitosterol has been
shown to be useful in cases of BPH by helping to reduce the normally elevated levels of
prostaglandins in these patients.
Status | Completed |
Enrollment | 160 |
Est. completion date | September 2016 |
Est. primary completion date | May 2016 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Male |
Age group | 40 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Age between 40 and 65 years - Only Male included - Has suffered from symptoms of BPH for at least the 6 months before Screening. - Has a prostate volume = 20 mL and = 70 mL as assessed by ultrasound - Has an IPSS = 8 at Screening and Baseline - Patients willing to give informed consent in writing Exclusion Criteria: - Neurogenic bladder dysfunction - Has bladder neck contracture or urethral stricture - Has acute or chronic prostatitis or urinary tract infection - Has a history of, prostate cancer or carcinoma of the prostate suspected on digital rectal exam. - Participation in any other clinical trial with in the last 30 days - Has resting systolic blood pressure (BP) > 160 mmHg or < 90 mmHg, or diastolic BP > 90 mmHg or < 60 mmHg at Screening. - Urine flow< 5mls/sec. - Use of any other herbal medications for treatment of BPH, associated symptoms and Erectile Dysfunction in past 1 month. - Has hematuria of unknown etiology. - Previous radiotherapy |
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label
Country | Name | City | State |
---|---|---|---|
India | Department of Urology, King George's Medical University, Lucknow, UP, India | Lucknow | Uttar Pradesh |
Lead Sponsor | Collaborator |
---|---|
Chemical Resources |
India,
Roehrborn CG. Benign prostatic hyperplasia: an overview. Rev Urol. 2005;7 Suppl 9:S3-S14. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Reduction in prostate volume | 12 weeks | No | |
Secondary | Improvement in urinary flow parameters | 12 weeks | No |
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