A study on quality of life in Prosthakola veekkam (Benign prostatic hyperplasia) patients taking siddha treatment
Not Applicable
- Conditions
- Health Condition 1: N401- Benign prostatic hyperplasia withlower urinary tract symptoms
- Registration Number
- CTRI/2023/02/049626
- Lead Sponsor
- ational Institute of Siddha
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.K/C/O Benign Prostatic Hyperplasia and newly diagnosed BPH
patients
2.Patients who would take 48 days of Siddha treatment for Prosthakola veekkam (BPH) at Ayothidoss Pandithar hospital NIS
3.Patients who are willing to give informed consent
Exclusion Criteria
1. Age below 50 and above 80 years
2.K/C/O Prostatic malignancy
3.K/C/O Urinary bladder calculus
4.Patients with prior history of prostatic/urethral surgery
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Difference in BPH Specific Quality of life scale will be assessed form baseline <br/ ><br>through endpoint with Benign Prostatic hyperplasia targeted siddha treatmentTimepoint: 4 months-Data collection <br/ ><br>2 months- Data analysis and outcome
- Secondary Outcome Measures
Name Time Method ILTimepoint: NI