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Effect Of Unani Formulation In Prostate disease

Effect Of Majoon e Rasheedi On Benign Prostatic Hyperplasia- A Randomized Open Labelled Comparative Clinical Study - BPH

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/04/041693
Enrollment
38
Registered
2022-04-06
Start date
Unknown
Completion date
Unknown
Last updated
2022-05-02

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

Conditions

Health Condition 1: N400- Benign prostatic hyperplasia without lower urinary tract symptoms

Interventions

Intervention1: Majoon-e-Rasheedi S. No. Drug Name Scientific Name Parts Used Quantity Majoon Rasheedi containing Piper cubeba Areca catechu Linn. Eugenia coryophyllata Pistacia lentiscus Linn. Trachy

Sponsors

National Institute of Unani Medicine Bengaluru
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Male patients about the age of 40 to 70 yrs. Patients having classical signs and symptoms of (BPH) like with increased urinary frequency, dysuria, urgency, dribbling, burning micturition, nocturia strains and incontinence of urine, etc. Prostate size - Grade I & II ultrasound based) USG findings (weight Flow rate >10 ml/s. Patients who will give their written informed consent and are able to do follow up.

Exclusion criteria

Exclusion criteria: Age below 40 years and above 70 years. P.S.A > 4 ng/ml Known case of stricture urethra. Active urinary tract infection. Carcinoma of prostate and abscess. Flow rate Patients of congenital deformities of the urogenital tract or any abdominoâ??pelvic pathology other than BPH. Systemic diseases such as Hypertension, Diabetes mellitus, tuberculosis, paralysis and Parkinsonism known cases of heart disease were excluded from the study. Previous B.P.H surgery.

Design outcomes

Primary

MeasureTime frame
Reduction in the prostate Volume Change in PVRU (Pre & Post) Improvement in Urine flow rate Qmax (Fortnightly) Decrease of (IPSS) International Prostate Symptom Score (Fortnightly) BPH Impact Index Timepoint: 45 days

Secondary

MeasureTime frame
ASSESMENT OF SAFETY PARAMETERS like CBP, ESR, AST, ALT, ALP, Blood Urea, Serum creatinine before and after the clinical trialTimepoint: 45 DAYS

Countries

India

Contacts

Public ContactProf Mohd Aleemuddin Quamri

National Institute of Unani Medicine, Bengaluru

drmaquamri@gmail.com9341072974

Outcome results

None listed

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