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Clinical study of Vibrance therapeutic water on digestive health, stress reduction, and glucose level control.

Phase 2
Conditions
Health Condition 1: K929- Disease of digestive system, unspecified
Registration Number
CTRI/2024/08/072329
Lead Sponsor
Mystic Kingdom Pvt. Ltd.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

Participants meeting all the following criteria will be eligible for the study:

1. Male and female participants aged 21-50 years (both inclusive); 2. BMI between 18.5 – 29.9 kg/m2; 3. Participants should self-report at least two of the following gastrointestinal symptoms: epigastric discomfort, heartburn, bloating, nausea, fullness in the stomach, abdominal pain, or anorexia; 4. Suffering from self-reported mild to moderate stress on the PSS scale score less than or equal to 26; 5. Participants must demonstrate their willingness to participate in the study and comply with its procedures by signing a written informed consent. 6. Subjects with or without type 2 diabetes, if diabetic should be on stable medication for at least the past 3 months and have HbA1c NMT 7.5%.(10 subjects will be enrolled which will be having type 2 diabetes)

Exclusion Criteria

Participants meeting any of the following criteria will not be eligible for the study:

1. Participants with major abdominal surgery, a history of inflammatory bowel disease or diverticular disease, celiac disease, allergic diseases, including asthma, psychiatric disorders and critical systemic illness as assessed by medical history, appropriate consultations and/or laboratory tests; 2. Actively having a gut infection; 3. History of or complications from malignant tumors; 4. Participant using or had used any probiotics, prebiotics herbs, dietary, nutraceutical, ayurvedic supplements or any other medicines for the digestive health, stress or glycemic control; 5. Females who are pregnant and have a positive urine pregnancy test/planning to be pregnant/lactating or not using reliable methods of contraception; 6. Participants with heavy alcohol consumption or smoking/tobacco consumption; 7. Participation in any other clinical study within the past 3 months or ongoing; 8. Any other reason that, in the opinion of the investigator, excludes the participant from eligibility for study participation.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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