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An Open Label, Two Arm, Clinical Study to evaluate the Efficacy and Safety of powder as an Nutritional Supplement for tiredness and illness

An Open Label, Two Arm, Clinical Study to evaluate the Efficacy and Safety of HQAP061801 powder as an Oral Nutritional Supplement for Occupational Work Fatigue and Post Illness Convalescence

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/09/021415
Enrollment
40
Registered
2019-09-25
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

None listed

Interventions

Intervention1: Quista Active: Open Label, Two Arm, Clinical Study. 40 Eligible subjects will be enrolled into two groups. Each group will have 20 subjects and will be advised to take HQAP 061801 at a

Sponsors

The Himalaya Drug Company
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Both male and female adult subjects between the age group of 2. More than 18 years to less than 60 years who are confirmed to have a history of work related fatigue as assessed through Fatigue assessment scale (FAS). 3. Both male and female adult subjects between the age group of More than 18 years to less than 60 years who are in post illness convalescence period. 4. Subject willing to refrain taking any other oral nutritional supplements during the study period. 5. Subjects willing to give written informed consent Subjects who had not participated in similar kind of study in last 4 week.

Exclusion criteria

Exclusion criteria: 1. Subject with clinically significant systemic illnesses treated with medication. 2. Subject with chronic illness which need immediate therapeutic intervention. 3. Subjects with chronic infectious condition treated with medications 4. Subjects who are hypersensitive to any of the ingredients, 5. Pregnant & lactating women.

Design outcomes

Primary

MeasureTime frame
Overall study compliance of the subject to the study medication Any adverse effects reported or observed during the study period Timepoint: The subject will be assessment visits are scheduled on day 1, day 30 days (telephonic) and at (End of Study) day 60 days.

Secondary

MeasureTime frame
Overall study compliance of the subject to the study medication Any adverse effects reported or observed during the study period Timepoint: The whole study duration is for 30 days with scheduled follow up visits at day 1, day 14, and day 30 day.

Countries

India

Contacts

Public ContactDr Palaniyamma

The Himalaya Drug Company

dr.palani@himalayawellness.com9686681830

Outcome results

None listed

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