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Role of pashanabheda kashaya and paataladi kashaya in the management of Prostate.

A Randomized Comparative Clinical Study To Evaluate The Efficacy Of Pashanabheda Kashaya And Paataladi Kashaya In The Management Of Vatashthila With Special Reference To Benign Prostatic Hyperplasia

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/03/031681
Enrollment
40
Registered
2021-03-03
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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: Pashanabheda kashaya: first make the kasaya then give to the patient for drink Control Intervention1: paataladi kashaya: first make the kashaya then give to the patient for drink

Sponsors

Dean Parul Institute of Ayurved
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: -Male aged between 40 to 85years -Having clinical features of Vatashtila or BPH like Granthivat Adhmana Mutrasangha Basti vedana Dribbling micturition Nocturia Increased frequency Urgency Weak stream Intermittency Straining Sensation of incomplete emptying

Exclusion criteria

Exclusion criteria: K/C/O uncontrol diabetic mellites,hypertension •CA prostate • Urethral stricture •Bladder neck stenosis •Neuropathy bladder dysfunction •Impaired renal function •Prostate (grade 4) •Patient indicated for prostectomy •Haematuria secondary to renal & bladder stone, •Anaemic patient with Hb below 6 gm%

Design outcomes

Primary

MeasureTime frame
symptoms like frequency, urgency, nocturia weakstream of urine etcTimepoint: 28 days

Secondary

MeasureTime frame
symptoms like frequency, urgency, nocturia weakstream of urine etcTimepoint: 28 days

Countries

India

Contacts

Public ContactDr Amitabh Bachchan Kumar

Parul Institute of Ayurved

dr.amitabhsingh5098@gmail.com9449685098

Outcome results

None listed

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