A comparitive study of individualised homoeopathic medicines and organopathic mother tinctures in renal calculi

Phase 3

Not yet recruiting

Brief Summary: This study is non - randomised, open - label, prospective, interventional, comparitive clinical trial to assess the effectiveness of individualised homoeopathic medicines selected with BBCR vis-a-vis organopathic mother tinctures selected with boericke repertory in cases of urolithiasis. The study will evaluate the extent of improvement in dysuria using VAS as an assessment scale and number of stones using x-ray KUB/USG evidences in cases of renal calculi using individualised homoeopathic medicines or organopathic mother tinctures and will also find the more effective method of treatment mentioned above.

Recruitment & Eligibility

Inclusion Criteria

1.Diagnosed cases with radiological evidence ( X-ray kidney/ureter/bladder and/or Ultrasound whole abdomen of calculi ) 2.Undiagnosed cases with symptoms of renal colic or history of renal colic with urinary complaints.
3.Asymptomatic cases with radiological evidence (X-ray KUB/USG).
4.Patients giving consent to participate in the study.
5.No history of expulsion of calculi after radiological investigations within one month period.

Exclusion Criteria

1.Cases with severe uremia, hydronephrosis, recurrent urinary tract infections or acute retention of urine for more than 24 hours.
2.Gross developmental defects or structural abnormality of kidney.
3.Pregnant women and Lactating mothers.
4.Cases with other severe systemic illness like hypertension, hypothyroidism, hyperparathyroidism, diabetes mellitus, etc.

Primary Outcome Measures

Name	Time	Method
2.To assess the effect of Individualised Homoeopathic Medicines selected with BBCR and of Organopathic Mother Tinctures selected with Boericke Repertory using pre and post X- ray KUB/USG evidences for number of stones.	1.Pre scores will be taken at baseline of treatment and post scores will be assessed at the end of 2 weeks. \| 2.Pre X-ray KUB/USG evidences first will be taken at the baseline of treatment and after evidences at the end of 12 weeks.
1.To assess the effect of Individualised Homoeopathic Medicines selected with BBCR and of Organopathic Mother Tinctures selected with Boericke Repertory using VAS scale pre and post treatment scores for dysuria.	1.Pre scores will be taken at baseline of treatment and post scores will be assessed at the end of 2 weeks. \| 2.Pre X-ray KUB/USG evidences first will be taken at the baseline of treatment and after evidences at the end of 12 weeks.

Secondary Outcome Measures

Name	Time	Method
To find the more effective method of treatment mentioned above in the study	12 months

Locations (1): Dr Girendra Pal Homoeopathic Hospital & Research Centre
🇮🇳
Jaipur, RAJASTHAN, India
Dr Girendra Pal Homoeopathic Hospital & Research Centre
🇮🇳Jaipur, RAJASTHAN, India
Dr Akanksha Sahu
Principal investigator
8377852765
akankshasahu.zz28@gmail.com