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An ayurvedic intervension for gastro-esophageal reflux disease

A Controlled Clinical Study to evaluate the effect of Sarivadya Hima over Vamana Dhauti in Amlapitta - Nil

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/069659
Enrollment
60
Registered
2024-06-28
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Health Condition 1: K21- Gastro-esophageal reflux disease

Interventions

None listed

Sponsors

Dr JANANI D RAO
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Subjects having at least 3 of the classical symptoms of Amlapitta as described in Ayurvedic literature will be included Symptoms must be present for atleast 3 days in a week for about 3 months to be included in the study Subjects who are willing to participate in the study

Exclusion criteria

Exclusion criteria: Previously diagnosed with or having any history of ulceration of stomach esophagus and duodenum and other systemic diseases such as hupertension cardiovascular ailmentsnephropathic and any type of malignant disorders Subjects who have undergone recent surgeries Subjects who are not fit for Vamana Dhauti Pregnant lady and lactating women

Design outcomes

Primary

MeasureTime frame
assesment of avipaka, klama, utklesha tikta amlaodgara gourava hrit kanta dahaa aruchi will be done to evatuate the effectiveness of vamana dhauti and Sarivadya Hima in AmlapittaTimepoint: at 15th day, 31st day and 46th day

Secondary

MeasureTime frame
Assessment of avipaka, klama, utklesha, tikta-amlodgara, gourava, hrit kanta daha, aruchi will be done to compare the efffectiveness of Vamana Dhauti, Vamana Dhauti with Sarivadya Hima, & Sarivadya Hima alone in AmlapittaTimepoint: 15th day 31st day 46th day

Countries

India

Contacts

Public ContactDR VENKATAKRISHNA K V

Government Ayurveda Medical College Mysuru

srisadguru@gmail.com9448572614

Outcome results

None listed

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