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Evaluate the efficacy of Yavadi Kwath in the management of Amlapitta (Hyperacidity)

Randomized controlled clinical trial to evaluate the efficacy of Yavadi Kwath in the management of Amlapitta(Hyperacidity) - Nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/05/087285
Enrollment
92
Registered
2025-05-21
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: K319- Disease of stomach and duodenum, unspecified

Interventions

None listed

Sponsors

C.s.m.s.s Ayurved Mahavidyalaya and Rugnalaya kanchanwadi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Gender- Irrespective of gender 2)Age- 18 years to 40 years 3)Patient having clinical sign and symptoms of Amlapitta as described in Madhav nidan Ref(Madhav nidan 51/2) Aavipak(indigestion) utklesh aruchi(Tastelessness) Amla udgar(Sour belching) Kanthadaha(Burning sensation in throat) Klama(Fatigue) Hruddah(Heartburn)

Exclusion criteria

Exclusion criteria: Pregnant and lactating women Patient with any GIT,Chronic illness and Abdominal complications Patient with diagnosed cases of Duodenal, Peptic and Gastric ulcers

Design outcomes

Primary

MeasureTime frame
Avipak Klama Utklesh will be decreasedTimepoint: 14 days

Secondary

MeasureTime frame
Amla udgar (Sour belching) Gaurav (Heaviness) Daha (Burning sensation) will be decreased Aruchi(Tastelessness)Timepoint: 14 days

Countries

India

Contacts

Public ContactDr Shubhangi Sarangdhar Pawar

CSMSS Ayurved Mahavidyalaya and Rugnalaya

dr.shrikantgdeshmukh@gmail.com9921553911

Outcome results

None listed

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