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To study the effectiveness of Yavasaktumantha during trekking activity.

Evaluation of effectiveness of Yavasaktumantha and Conventional ORS solution during vigorous activity (trekking)among healthy adult individuals:Randomised Controlled Trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/08/020686
Enrollment
82
Registered
2019-08-13
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: yavasaktumantha: Yavasaktu (one part) will be mixed very well by adding cow ghee (one fourth part), Then four parts of water will be added in Yavasaktu and then churned till Mantha will

Sponsors

Dr Darshana Chaudhari
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Apparently healthy individual. Individuals with age limit of 18 to 60 years. Individuals of either gender will be included

Exclusion criteria

Exclusion criteria: Individuals below 18 and above 60 years of age. Individuals having Diabetes mellitus (Type I and type II), Tuberculosis of any body part, Hypertension, Anaemia, Lung disease, Cardiovascular disease. Individuals having major illness or operated recently for any cause. Individuals having acute lumbar spondylosis and cervical spondylosis or any acute illness.

Design outcomes

Primary

MeasureTime frame
Yavasaktumantha is more effective than Conventional ORS Solution in Thirst (Pipasanashan), Fatigue (Shramanashan) and Strength depletion (Balahani).Timepoint: 1.Trial day 2.next to trial day.

Secondary

MeasureTime frame
Yavasaktumantha is not effective than Conventional ORS Solution in Thirst (Pipasanashan), Fatigue (Shramanashan) and Strength depletion (Balahani).Timepoint: 1.trial day. 2 next to trial day.

Countries

India

Contacts

Public ContactDr Mandar Karve

Y.M.T. Ayurvedic Medical College

mandarkarve82@yahoo.co.in9422552908

Outcome results

None listed

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