Skip to content

To Study the Effect of Gudaadi Mandoor in Anemia of Adolescent Girls

Clinical study to evaluate the efficacy of Gudaadi Mandoor in the management of Pandu (Anemia) in Adolescent girls

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/08/020513
Enrollment
60
Registered
2019-08-02
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Intervention1: Trial drug (Gudaadi Mandur): The proposed trial drug Gudaadi Mandoor 15-18mg /kg/day in two divided doses for 8 weeks Control Intervention1: Group B:IFA: B. Control: IFA Tablets

Sponsors

National Institute of Ayurveda Jaipur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Female subjects aged between 12-15 years. 2) Subjects with iron deficiency Pandu (Anemia) (Hb gm%: 7 gm% to 11.9 gm %). 3) Subjects whose parents are willing to give consent for clinical trial.

Exclusion criteria

Exclusion criteria: 1) Hemoglobin gm% 2) Subjects suffering from major systemic illness necessitating long term treatment. 3) Subjects with evidence of malignancy. 4) Subjects with concurrent serious hepatic dysfunction (defined as AST and/or ALT >3 times of the upper normal limit) or renal dysfunction (defined as S. creatinine >1.2mg/dl), uncontrolled pulmonary dysfunction (asthmatic and COPD patients)

Design outcomes

Primary

MeasureTime frame
Improvement in Hb%Timepoint: 8 weeks

Secondary

MeasureTime frame
Clinical Improvement in symptoms of anemia in adolescent girlsTimepoint: 8 weeks

Countries

India

Contacts

Public ContactPriyanka Kumari

National institute of ayurveda, Jaipur

priyankatripathy02@gmail.com7903452913

Outcome results

None listed

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