MedPath

A study to know the effectiveness of Ayurveda Supplements and Yoga Protocol in preventing and reducing the symptoms of Acute Mountain Sickness.

Phase 3
Registration Number
CTRI/2023/03/051028
Lead Sponsor
Central Council for Research in Ayurvedic Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. Apparently healthy Indian Army volunteers aged 18-50 years irrespective of gender

2. Indian Army volunteers who will be found fit for deployment to high altitude areas (under the Ladakh region of the Northern Command of Indian Army)as per the existing guidelines

3. Indian Army volunteers who will be either deployed to high altitude area for the first time or resumed their deployment after break

4. Willing to participate and provide written informed consent.

Exclusion Criteria

1. History of underlying cardiovascular disease or a clinically significant ECG abnormality, cerebrovascular disease, pulmonary disease, neurological disease, psychiatric illness, major venous thromboembolism (deep vein thrombosis/pulmonary embolism/cerebrovascular thrombosis), sickle-cell disease, metabolic diseases, malignancy, glaucoma etc.

2. Previous history of pulmonary edema or severe physiological response to high altitude such as high altitude pulmonary edema

3. History of uncontrolled DM (HbA1C > 8.0) and uncontrolled hypertension ( > 140/90 mm Hg) even after medications

4. BMI >= 30 kg/m2

5. History of abnormal hepatic function (AST and/or ALT, > 2 times upper normal limit) or abnormal renal function (serum creatinine 1.2 mg%)

6. Subjects on any concomitant conventional medication on regular basis

7. History of surgery within six months prior to screening

8. History of blood transfusion or any blood products within 90 days prior to screening

9. History of chain smoking, alcohol use disorder and substance abuse

10. Any other condition which the P.I. thinks may jeopardize the safety of the subjects

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Primary: <br/ ><br>â?¢Incidence of AMS assessed through Lake Louise Scoring System (2018) <br/ ><br>â?¢Proportion of participants with LLSS score â?¥ 6.Timepoint: Baseline to first seven days, then on the first four days at each altitude.
Secondary Outcome Measures
NameTimeMethod
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