To study the effect of kayyonyadi syrup in iron deficiency anemia.

A single arm clinical study to evaluate the efficacy of kayyonyadi syrup in the management of Pandu with special reference to Iron deficiency anemia in children age group 1 to 12 years. - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/05/067238

Enrollment

Registered

2024-05-13

Start date

Unknown

Completion date

Unknown

Last updated

2024-05-27

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 Health Condition 2: D509- Iron deficiency anemia, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Children having HB% between 9mg/dl. Patients having iron deficiency anemia.

Exclusion criteria

Exclusion criteria: Patients having k/c/o Sickle cell anemia, Megaloblastic anemia, Aplastic anemia, Pernicious anemia etc Patient present with k/c/o any bleeding disorder, thrombocytopenia, Hemorrhoids, Thalesemia.

Design outcomes

Primary

Measure	Time frame
To evaluate the efficacy of Kayyonyadi Syrup on Hb concentration or Haematological parameters.Timepoint: 60 days study with follow up of 30th and 60th days (0,30,60 days)	—

Secondary

Measure	Time frame
To study signs & symptoms of anemia i.e Panduta(Pallor),Daurbalya(General weakness),Akshikutashotha(Peri-orbital edema),Pindikodveshtana(Leg cramps),Hrutaspandana(Palpitation)Timepoint: 60 days study with follow up of 30th & 60th days.	—

Countries

India

Contacts

Public ContactDr Ankit Patil

Dr. D.Y.Patil College of Ayurved and Research Center

sbhagwat777@gmail.com7588562700

Outcome results