Study to evaluate the efficacy of Nishalauha and Vasaadi Kwatha in Pandu Roga

A clinical study to evaluate the efficacy of Nishalauha and Vasaadi Kwatha in the management of Pandu Roga w.s.r. to Iron deficiency Anaemia - Nil

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/06/068815

Enrollment

Registered

2024-06-12

Start date

Unknown

Completion date

Unknown

Last updated

2025-09-15

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

Conditions

Health Condition 1: D509- Iron deficiency anemia, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Patients presenting with signs and symptoms of pandu roga having haemoglobin 8-12gm% in males and 8-11gm% in females.

Exclusion criteria

Exclusion criteria: patients suffering from chronic respiratory cardiac renal disorders, Diabetes mellitus, pregnant and lactating mothers , CA, TB

Design outcomes

Primary

Measure	Time frame
Increase in haemoglobin concentration Timepoint: patients will be assess after 4 weeks and at the end of trial.	—

Secondary

Measure	Time frame
To Assess the clinical safety & untoward effects of Nishalauha & Vasaadi Kwatha in the management of Pandu Roga w.s.r. to Iron Deficiency AnaemiaTimepoint: 8 weeks	—

Countries

India

Contacts

Public ContactDr Prerna

Rajiv Gandhi Govt Post Graduate Ayurvedic College and hospital Paprola

Dr.geeti@gmail.com7018817072

Outcome results