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Individualized Homoeopathic medicine and Chimaphila umbellata Mother tincture in the Treatment of Benign Prostatic Hyperplasia

Not Applicable
Conditions
Health Condition 1: N40- Benign prostatic hyperplasia
Registration Number
CTRI/2022/07/044123
Lead Sponsor
ational Institute Of Homoeopathy
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

a)Patients presenting symptoms of Benign Prostatic Hyperplasia with or without evidence of bladder outflow obstruction (AUASS more than 7) b)Patients suffering from cases of Benign Prostatic Hyperplasia diagnosed radiologically (USG-PELVIS) and ultrasonographical examination of Prostate weight more than 20g/20cc and RUV of more than 30ml c)Patients already undergoing regular therapy for BPH, provided the medications are stopped completely at least 2weeks prior study entry d)Male patients of all religions and of different socioeconomic status e)Patients with known but controlled systemic diseases f)Patients giving written consent to participate in the study

Exclusion Criteria

a)Patients with Serum Prostate specific antigen (PSA) more than 4 nmol/mL to rule out suspected

prostatic malignancy

b)Cases suffering from uncontrolled systemic illness or life-threatening conditions.

c)Patient suffering from complete retention of urine for more than 24hrs.

d)Patient with frequent urination or retention of urine due to systemic or neurological disorder.

e)Patient suffering from neurogenic bladder or urethral stricture

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
On the basis of score obtained from the AMERICAN <br/ ><br>UROLOGICAL ASSOCIATION Symptom Score, cases according to intensity will be <br/ ><br>grouped into <br/ ><br>1-7 mildly symptomatic <br/ ><br>8-19 moderately symptomatic <br/ ><br>20-35 severely symptomatic. <br/ ><br> Marked improvement â?? decrease of 70% or more in AUASS <br/ ><br> Moderate improvement â?? decrease of 50-70% in AUASS <br/ ><br> Mild improvement - decrease of less than 50% in AUASSTimepoint: At base line, at 3rd month and at 6th month
Secondary Outcome Measures
NameTimeMethod
The reduction of size of prostate gland and RUV, will be <br/ ><br>recorded using USG-PELVISTimepoint: At base line and at 6th month
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