Comparative clinical study of godanti-gairika vati and godanti-kasisa vati in pandu ( iron deficiency anaemia) and pharmaceutico-analytical study of these two vati.
Phase 3
- Conditions
- Health Condition 1: D509- Iron deficiency anemia, unspecified
- Registration Number
- CTRI/2022/11/047470
- Lead Sponsor
- Principal, R.G.G.P.G. Ayurvedic College and Hospital Paprola, Distt. Kangra, H.P.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients willing for clinical trial and ready to give written consent.
2.Patients having Hb more than 8gm% but less than 10gm%.
3.Patients possessing sign and symptoms of Pandu roga on the basis of diagnostic criteria.
4.Patients not having any associated chronic ailment.
Exclusion Criteria
1.Patients having Hb less than 8gm% or more than 10 gm %.
2.Patients with further complications of Pandu roga such as hridroga, shotha etc.
3.Congenital anaemia like sideroblastic anaemia, congenital dyserythropoetic anaemia, thalessemia, sickle cell anaemia, aplastic anaemia etc.
4.Patients having blood loss due to haemorrhoids, ulcers and epistaxis.
5.Patients suffering from AIDS, Cancer, TB, Diabetes mellitus or any other severe systemic dissorder.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Relieve in symptoms like palpitations, dryness, lack of sweating and fatigue, tinnitus, pallor, generalised weakness, vertigo, excessive sleep, pain in the calf muscle, swelling around the eye, anorexia.Timepoint: 45 days trial period
- Secondary Outcome Measures
Name Time Method Complete remission of sign and symptoms. <br/ ><br>Improved haemoglobin levels of patients.Timepoint: Follow up 1 month after completion of trial