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Effect of Basti (Ayurvedic therapy) on gut health of obese persons

Effect of a therapeutic course of Basti on gut microbiome in obese individuals - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/104142
Enrollment
30
Registered
2026-02-18
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Health Condition 1: Z682- Body mass index (BMI) 20-29, adult

Interventions

None listed

Sponsors

Ministry of Ayush
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Overweight and obese individuals of either sex in the age group of 30-49 years with BMI above 23.0kg/m and below 35.0 kg/m (WHO Asia Pacific Guideline) Individuals willing to participate voluntarily & ready to follow and abide by all study procedures

Exclusion criteria

Exclusion criteria: Individuals not eligible for basti (anarha) procedure such as those with any ano-rectal pathology (e.g. haemorrhoids, fissure or fistula), or female participants in the premenstrual phase with anticipated onset of menstruation within two weeks of enrolment Individuals with known case of diabetes who have been prescribed anti-diabetic drugs or with HbA1c levels more than 7percent Individuals with known case of hypertension or Systolic pressure more than 140 mm Hg and diastolic pressure more than 90 mm Hg with or without medication Individuals who were treated with Allopathic or Ayurvedic medicines or have had surgery for weight loss/slimming/weight gain or individuals currently participating in organized weight reduction program (1 month before study enrolment) Individuals with secondary obesity caused by endocrine disorders like PCOS, or due to medications like Corticosteroids, Antidepressants, Antipsychotics Individuals with a known history of malignancy, asthma, chronic cough, coronary heart disease, psychological problems, chronic kidney and liver disease or receiving immunosuppressive medication Individuals with history or evidence of any other condition or disease that would interfere with the study evaluation, procedures, or completion making participants unfit to recruit Individuals with a history of antibiotic treatment or pro & pre-biotic supplements (1 month before study enrolment) Female participants who are pregnant or lactating

Design outcomes

Primary

MeasureTime frame
Gut microbiome Analysis Short-Chain Fatty Acids (SCFA) and Inflammatory profile (Interleukin-6 and lipopolysaccharide) Anthropometry (Hip & waist circumference, Waist-Hip Ratio, Neck Circumference) Skinfold thicknesses (Biceps, Triceps, Subscapular & Supra-iliac) Body Composition (Total body fat, visceral fat) Timepoint: Gut microbiome Analysis: Assessed on Days 0,17, 49, 79, 109 and 139 Short-Chain Fatty Acids (SCFA) and Inflammatory profile : Assessed on Days 0,17, 49 and 139 Anthropometry : Assessed on Days 0,17, 49, 79, 109 and 139 Skinfold thicknesses : Assessed on Days 0,17, 49, 79, 109 and 139 Body Composition: Assessed on Days 0,17, 49, 79, 109 and 139

Secondary

MeasureTime frame
Haematological parameters (Lipid Profile, Fasting Blood Sugar and Fasting Insulin) AgnibalaTimepoint: Haematological parameters : Assessed on Days 0,17, 49 and 139 Agnibala : Assessed on Days 0,17, 49 and 139

Countries

India

Contacts

Public ContactPooja Londhe

Interaction Research School for Health Affairs, Bharati vidyapeeth (Deemed to be University)

supriya.bhalerao@bharatividyapeeth.edu9869555272

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026