To study the effect of Dashamoola Siddha Taila Matrabasti and Uttarbasti in the management of Mootraghata W.S.R. to Benign Prostatic Hyperplasia
- Conditions
- Health Condition 1: N401- Benign prostatic hyperplasia withlower urinary tract symptoms
- Registration Number
- CTRI/2022/07/043639
- Lead Sponsor
- Government Akhandanand Ayurved College Ahmedabad
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 30
1. Patients presenting with classical signs and symptoms of
Mootraghata/BPH like Incomplete emptying, Increased Frequency,
Intermittency, Urgency, Weak stream,Straining, Nocturia, Painful
mituration, Burning micturition
2. Male patient Age between 40-80 year
3. Controlled case of Diabetes mellitus (RBS upto 180 mg/dl) and
Hypertension (upto 150/90 mm Hg)
1. CA Prostate
2. Urethral stricture
3. Benign tumour of urethra
4. Malignant tumour of urethra
5. Urethral injury, urethral calculi
6. Age above 80 years and below 40 years
7. Patients with systemic diseases like uncontrolled Hypertension (more
than 150/90 mm Hg) and uncontrolled Diabetes mellitus (RBS more than
180 mg/dl),Tuberculosis, VDRL, STD, HIV, HBsAg
8. Known case of heart disease
9. According Ayurveda point of view, Matrabasti should not be
administered in the persons having Ajirna and who has slept during
day time
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Result will be assased on the basis of relief sign and symptoms of Mootraghata <br/ ><br> <br/ ><br>ResultDescription <br/ ><br>Subjective Criteria :- <br/ ><br>International Prostate Symptom Score (IPSS) <br/ ><br> <br/ ><br>Objective Criteria :- <br/ ><br>Prostatic size (volume) <br/ ><br>Urine Flow Rate <br/ ><br>Residual Urine Volume <br/ ><br> <br/ ><br> <br/ ><br>Timepoint: 21 Days
- Secondary Outcome Measures
Name Time Method Comparing the effect of both procedures in the management of Mootraghata <br/ ><br>ResultDescription: <br/ ><br>Complete cure - 100% relief in subjective, objective findings and IPSS parameters <br/ ><br>Maximum improvement - 76% to 100% relief in subjective, objective findings and IPSS parameters <br/ ><br>Moderate improvement - 51% to 75% relief in subjective, objectivefindings and IPSS parameters <br/ ><br>Mild improvement - 26% to 50% relief in subjective, objective findings and IPSS parameters <br/ ><br>Unchanged - Up to 25% relief in subjective, objectivefindings and IPSS parametersTimepoint: 2 weeks