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Promoting the Siddha interventions for Iron deficiency Anemia (Pandu) among rural women / Men at Adolescent age (10 to 19) in Southern districts of Madurai and Theni - Tamil Nadu.

Promoting the Siddha interventions for Iron deficiency Anemia (Pandu) among rural women / Men at Adolescent age (10 to 19) in South districts Madurai and Theni - Tamil Nadu.

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/02/049974
Enrollment
1500
Registered
2023-02-22
Start date
Unknown
Completion date
Unknown
Last updated
2023-03-06

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

Conditions

Health Condition 1: D50- Iron deficiency anemia

Interventions

Intervention1: Tab. Annabedi Chendooram : Tab. Annabedi Chendooram 1 (100 mg)after food B.D oral route for 90 days Intervention2: Tab.Bavana kadukai: Tab.Bavana kadukai 1 (500mg) B.D After food. Oral

Sponsors

Ministry of Ayush
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients /Guardian who are willing to sign the informed consent. Participants from the same project area. Participants willing to participate.

Exclusion criteria

Exclusion criteria: Age less than 10 years and more than 19 years, Pregnancy and lactation Congenital heart disease, hepatic, bleeding disorders, Sickle cell Anemia, Cancer, Renal failure. Patients with chronic diseases, inherited defects Patients with infectious diseases. Based on Laboratory investigations: Patients who do not give blood samples for investigation.

Design outcomes

Primary

MeasureTime frame
To promote the Siddha interventions for Anemia (Pandu) among rural women /Men at adolescent age (10 to 19) in South districtsâ??Madurai and Theni- Tamil Nadu. The siddha medication for anemia is given for 90 days to the subject and the outcome is monitored. Timepoint: 90 days

Secondary

MeasureTime frame
The increase in Haemoglobin content after 90 days of treatment with Siddha medicine will be documented statistically. Timepoint: 90 days;The quality of life will be assessed both before and after treatment using RAND 36 â?? Item health survey. Timepoint: 90 days

Countries

India

Contacts

Public ContactS ELANSEKARAN

National Institute Of Siddha

sekarnis78@gmail.com9962536907

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026