Use of navayas lauh(type of churna preparation)in the management of garbhini pandu (Iron deficiency anemia in pregnancy)

Clinical study to evaluate the efficacy of Navayas Lauha in the management of Garbhini Pandu w.s.r to Iron deficiency Anemia in Pregnancy - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/08/092320

Enrollment

Registered

2025-08-04

Start date

Unknown

Completion date

Unknown

Last updated

2025-08-18

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: Pregnant woman age group 20-40 yrs 1st,2nd and 3rd trimester Primi and multigravida both Hb% between 7gm % to 10 gm %

Exclusion criteria

Exclusion criteria: Age below 20 year and above 40 year All type of anemia other than iron deficiency Anemia All patient in high risk pregnancy group other than iron deficiency Anemia All major systemic disease Hb gm % below 7gm % and above 10 gm %

Design outcomes

Primary

Measure	Time frame
Improvement in haemoglobin parameterTimepoint: The trial drug will be given for 3 months with anupana and follow up will be done after cessation of medicine in 4 months	—

Secondary

Measure	Time frame
Reduction of pallor,fatigue and loss of appetite and palpitationTimepoint: After analyzing all the parameters the result will be assessed on the basis of symptomatic relief and improvement Partially improvement after 15 days-patient get 30percent relief from sign and symptoms Improvement after 1 month patient get 40-50 percent relief from sign and symptoms Improvement after 2 months patient get 60-80 percent relief from sign and symptoms Cured after 3 months patient get 80-100 percent relief from signs and symptoms.	—

Measure

Time frame

Reduction of pallor,fatigue and loss of appetite and palpitationTimepoint: After analyzing all the parameters the result will be assessed on the basis of symptomatic relief and improvement Partially improvement after 15 days-patient get 30percent relief from sign and symptoms Improvement after 1 month patient get 40-50 percent relief from sign and symptoms Improvement after 2 months patient get 60-80 percent relief from sign and symptoms Cured after 3 months patient get 80-100 percent relief from signs and symptoms.

—

Countries

India

Contacts

Public ContactDr Bhappil Sharma

Vaidya Yagya dutt sharma Ayurved Mahavidyalaya

drbhapilsharma@gmail.com7018687930

Outcome results