BPH management by Ayurveda procedure by pushing oil in urethral opening

Phase 2

Completed

• Conditions: Benign prostatic hyperplasia withlower urinary tract symptoms. Ayurveda Condition: Mootravaha Srotas Vyadhi,

• Registration Number: CTRI/2021/03/032260
• Lead Sponsor: Institute of Teaching and Research in Ayurveda

Brief Summary

The research study entitled “Comparative clinical effect of Balataila as Uttara Basti and Matra Basti along with Kanchanar Guggulu in management of Mootraghata (Benign prostate hyperplasia) A open-label clinical trial -[BPH] â€ Aim and Objective of this study was to compare the clinical effect of *Balataila* in the form of *Uttara Basti* and *Matra Basti* along with *Kanchanar Guggulu* orally in the management of *Mootraghata*(BPH). In this trial total of 100 Patients having signs & symptoms of *Mootraghata* will be divided into two groups 50 in each group by computer generated Random number table method. In Group A 50 Patients will be treated with Balataila Uttarbasti for the period of 7 days with 7 days interval along with oral medication of Kanchanar Guggulu 2 Tab Thrice a day for 30 days while in Group B 50 Patients will be treated with *Balataila* *Matra Basti daily* along with oral medication of Kanchanar Guggulu 2 Tab Thrice a day for 30 days. Follow will for 2 months in both the groups. Before treatment, routine hematological, biochemical, urine examination will be carried out. The assessment will be done after the completion of therapy in parameters including subjective and objective criteria like Urine flow rate (UFR), Post voidal residual urine (PVRU), and Size of prostrate by USG. Effect of therapy will be assessed statically after completion of study in stipulated time

Detailed Description

Not available

Study Timeline

• Study Start: 2021-03-29
• Study Completion: 2022-06-16
• Last Update Posted: 2023-05-30

Recruitment & Eligibility

• Status: Completed
• Sex: Male
• Target Recruitment: 100

Inclusion Criteria

1.Grade 1 to Grade 3 BPH 2.Weight of prostate 30 to 85 gm 3.Patients having signs and symptoms of Mootraghata (BPH) 4.Patients with controlled diabetes mellitus 5.Patient with controlled blood pressure.

Exclusion Criteria

• 1.Age below 40years and above 60 years 2.Grade 4 BPH 3.Weight of prostate more than 85 gm 4.Patients with uncontrolled Diabetes mellitus (FBS more than 140mg/dl PPBS more than 180mg/dl) 5.Patient of Uncontrolled Hypertension ICD-10(BP more than 140/90 mm of Hg) 6.Known case of cardiac diseases.
• 7.Patients of malignancy, congenital deformities of the urogenital tract, or any abdominopelvic pathology other than BPH 8.Tuberculosis Paralysis Parkinsonism etc will be excluded.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Relief in signs and symptoms of BPH	one month

Secondary Outcome Measures

Name	Time	Method
Relief in signs and symptoms of BPH	2 month

Trial Locations

Locations (1)

Institute of Teaching and Research in Ayurveda Jamnagar; 🇮🇳 Jamnagar, GUJARAT, India

Institute of Teaching and Research in Ayurveda Jamnagar

🇮🇳Jamnagar, GUJARAT, India

Neeraj Kumar

Principal investigator

7231053235

Ayurkaushalam@gmail.com