A Clinical study to evaluate effect of single ayurvedic drug therapy in Pandu (Iron deficiency Anaemia)
Phase 2
- Conditions
- Health Condition 1: D759- Disease of blood and blood-formingorgans, unspecifiedHealth Condition 2: D759- Disease of blood and blood-formingorgans, unspecified
- Registration Number
- CTRI/2024/02/062297
- Lead Sponsor
- Tilak Ayurved Mahavidyalaya,
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Women of reproductive age group of 15 to 49 years
patients diagnosed with iron deficiency anaemia
patients having symptoms of panduta, dourbalya, shwas,hritspandan, akshi koot shoth
patients having haemoglobin less than 12
Exclusion Criteria
patients having haemoglobin less than 7
patient suffering from haematological disorder,gynacological diseases and systemic disorders
pregnant females and lactating mothers
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Minimum 50% increase in Hb should be observed after the completion of the trial in 60 daysTimepoint: Baseline, 15th day, 30th day, 45th day, 60th day
- Secondary Outcome Measures
Name Time Method recurrence of pallor,generalized weakness, dyspnoea,giddinesTimepoint: 60 days