Health Condition 1: N184- Chronic kidney disease, stage 4 (severe)
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Participants of either gender, aged twenty one to sixty five years, with a confirmed diagnosis of Chronic Kidney Disease up to Stage or Grade Four as per KDIGO criteria with estimated glomerular filtration rate greater than fifteen and smaller than sixty millilitres per minute per one point seven three square metre. Only clinically stable Grade Four patients who were not requiring immediate Renal Replacement Therapy at the time of enrolment. Participants who were willing to provide written informed consent. Participants who were not registered in any other research project in the last twelve weeks.
Exclusion criteria
Exclusion criteria: Participants with active Tuberculosis, malignancy, or any other uncontrolled systemic illness. Pregnant or lactating women. Participants with severe anaemia with haemoglobin smaller than six grams per decilitre. Participants with uncontrolled Diabetes with haemoglobin A one C greater than nine or uncontrolled Hypertension with blood pressure greater than one hundred sixty by one hundred millimetres of mercury. Participants with HIV associated nephropathy or transplant allograft failure. Known cases of renal artery stenosis or renal neoplasm. Participants with a history of kidney transplantation. Participants with congenital renal diseases such as Autosomal Dominant Polycystic Kidney Disease, Autosomal Recessive Polycystic Kidney Disease, Congenital Nephrotic Syndrome of Finnish type, Alport Syndrome, Fabry Disease, and Juvenile Nephronophthisis. Participants with acute kidney injury, rapidly progressive renal failure, or any complications necessitating immediate Renal Replacement Therapy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Improvement in estimated Glomerular Filtration Rate (eGFR) from baseline to end of treatment.Timepoint: 0th, 9th, 31st and 61st days. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.Improvement in routine laboratory investigations. 2.Improvement in clinical signs & symptoms of CKD 3.Improvement in Quality of Life assessed using KDQOL-36 questionnaire.Timepoint: 0th, 9th, 31st & 61st days. | — |
Countries
India
Contacts
All India Institute of Ayurveda, New Delhi.