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Naadi Examination in Detecting Patients with Kidney Diseases.

Diagnostic Accuracy of Naadi Parisodhanai (Siddha Pulse Examination) in Detecting Individuals with Renal Pathology Attending National Institute of Siddha-A Blinded Diagnostic Study - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/02/104900
Enrollment
157
Registered
2026-02-26
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: N183- Chronic kidney disease, stage 3 (moderate) Health Condition 2: N182- Chronic kidney disease, stage 2 (mild) Health Condition 3: N184- Chronic kidney disease, stage 4 (severe) Health Condition 4: N181- Chronic kidney disease, stage 1 Health Condition 5: N185- Chronic kidney disease, stage 5 Health Condition 6: N179- Acute kidney failure, unspecified

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil Intervention3: Nil: Nil Intervention4: Nil: Nil

Sponsors

National Institute of Siddha
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: CASES: Participants will be eligible if they: Are male or female, aged 18 65 years Known case of renal disease with abnormal Renal findings. Participants will be included in the case group as per KDIGO (Kidney Disease Improving Global Outcomes) Guidelines. Renal disease marked by lowered eGFR Estimated glomerular filtration rate (eGFR) less than 90 millilitres per minute per1.73 square metre (CKD-EPI) Excretion of urinary proteins. Spot urine ACR greater than or equal to 30 milligrams per gram. (Albumin to creatinine ratio) Renal pathologies detected by imaging studies. CONTROLS: Age: 18-65 eGFR greater than or equal to 90 millilitres per minute per 1.73 square metre (normal function) Spot urine ACR less than 30 milligrams per gram No evidence of renal pathologies on imaging. Patients with any clinical conditions which does not act as a confounder in diagnosing Renal pathology.

Exclusion criteria

Exclusion criteria: CASES: Participants will be excluded if they: Belong to vulnerable group (pregnant and lactating women, children). Recent urinary tract instrumentation/surgery (less than 48h). Patients in emergency conditions/post- operative hospitalised patients. Known systemic illness affecting kidney function independently (e.g., advanced heart failure, severe liver disease, sepsis) where attribution to renal pathology is uncertain. CONTROLS: Vulnerable group (Pregnant and lactating women, children)

Design outcomes

Primary

MeasureTime frame
Specificity and Sensitivity of Naadi examination for the diagnosis of Renal pathology will be obtained at baseline.Timepoint: Baseline

Secondary

MeasureTime frame
Positive Predictive Value (PPV) & Negative Predictive Value (NPV) of Naadi examination for Renal pathology will be estimated at baseline. Positive Likelihood Ratio & Negative Likelihood Ratio of Naadi examination will be calculated at baseline. Pretest odds & Posttest odds of Renal pathology based on Naadi examination will be evaluated at baseline. Diagnostic performance of Naadi examination will be assessed using ROC curve analysis & Area Under the Curve (AUC) at baseline. Different Naadi patterns if observed in different stages of Renal pathology will be documented at baseline. Yakkai Ilakkanam for Renal pathology patients will be documented through validated questionnaires at baseline.Timepoint: Baseline

Countries

India

Contacts

Public ContactProf Dr G J Christian

National institute of Siddha

christianvijila@gmail.com9962545930

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026