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A Study to Test the Safety and Benefits of Hb Vista Ayurvedic Capsule for Anemia.

An Open-Label, Single-Arm, Single-Centered Clinical Study To Evaluate The Safety And Efficacy Of Hb Vista Ayurvedic Capsule In Patients With Anaemia. - Nil

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/01/078934
Enrollment
60
Registered
2025-01-17
Start date
Unknown
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

Health Condition 1: D649- Anemia, unspecified

Interventions

None listed

Sponsors

Ram Swaroop Pharmacy
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients of either sex, aged 18 to 65 years. 2.Patients diagnosed with anaemia and haemoglobin levels lessthan 12 g per dL for women and lessthan 13g perdL for men. 3. Willingness to provide informed consent and comply with all study procedures. 4. Ability to attend study visits and follow the treatment plan. 5. General Health: Patients in generally stable health, with anaemia as their primary condition Mainly severe anemia cases.

Exclusion criteria

Exclusion criteria: 1. Pregnancy and Lactation Pregnant or lactating women are excluded due to safety concerns. 2. Severe Anaemia Patients with a history of chronic or congenital anaemia. 3. Recent Transfusions Patients who have undergone blood transfusions within the past three months. 4. Systemic Diseases Patients with systemic diseases like uncontrolled hypertension, uncontrolled diabetes, or tuberculosis. 5. Allergies Known allergies or hypersensitivity to any of the ingredients in HB Vista. 6. Concomitant Diseases Patients with other severe medical conditions that could interfere with the study outcomes or pose a risk to patient safety

Design outcomes

Primary

MeasureTime frame
Change in haemoglobin concentration is in g per dL from baseline to the end of the study period. The main outcome measure will be the increase in haemoglobin levels in patients from the start to the completion of treatment.Timepoint: Day0, Day1,Day20, Day40, Day60

Secondary

MeasureTime frame
Improvement in Quality of Life is Measured using a validated QoL scale to be defined, capturing patient-reported outcomes related to well-being, energy levels, and ability to perform daily tasks.Timepoint: Day0, Day1,Day20, Day40, Day60

Countries

India

Contacts

Public ContactMs Arpita Malgi

SAMAHITHA RESEARCH SOLUTIONS

satyalm@samahitha.com9739001749

Outcome results

None listed

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