A clinical study to evaluate the effectiveness of simhayadi kwatha and patoladipanchanga kwatha in the treatment of amlapitta (Gastro esophageal reflex disease)

A randomized comparative clinical study to evaluate the efficacy of simhasyadi kwatha and patoladipanchanga kwatha in management of amlapitta - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/07/070382

Enrollment

Registered

2024-07-10

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: K219- Gastro-esophageal reflux disease without esophagitis

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1. Subject of either sex. 2. Subject within the age group 18-60 yrs. 3. Subjects with clinical features of Amlapitta such as Avipaka, Klama, Uthklesha, Tikta Amlodgara, Gourava, Hruthkanta daha, and Aruchi will be included. 4. Subjects with controlled systemic disorder such as DM, HTN, etc will be included. 5. Subjects who are willing to give written consents for the study.

Exclusion criteria

Exclusion criteria: 1. Pregnant and Lactating women 2. Subjects with uncontrolled systemic disorder such as Diabetes mellitus, Hypertension, etc 3. Subject diagnosed with Gastro- intestinal disorders like peptic ulcer, pancreatic and hepatic disorders. 4. Subjects with history of haematemesis, malena and other systemic disorders that may interfere with the clinical trial.

Design outcomes

Primary

Measure	Time frame
Effect of treatment will be assessed on the basis of changes found in the gradation of the both individual and overall parameters according to their severity before, during and after treatment. SUBJECTIVE PARAMETERS Avipaka (digestion) Klama (tiredness) Uthklesha (nausea) Tikta amlodgara ( sour and bitter belching) Gourava (heaviness of body) Hruthkanta daha (burning sensation of throat ) Aruchi (anorexia)Timepoint: 30 DAYS	—

Measure

Time frame

Effect of treatment will be assessed on the basis of changes found in the gradation of the both individual and overall parameters according to their severity before, during and after treatment. SUBJECTIVE PARAMETERS Avipaka (digestion) Klama (tiredness) Uthklesha (nausea) Tikta amlodgara ( sour and bitter belching) Gourava (heaviness of body) Hruthkanta daha (burning sensation of throat ) Aruchi (anorexia)Timepoint: 30 DAYS

—

Secondary

Measure	Time frame
NOT APPLICABLETimepoint: NOT APLLICABLE	—

Countries

India

Contacts

Public ContactDr vijayalakshmi Teggi

ALN RAO Memorial ayurvedic medical college koppa

keshavamdkc@gmail.com9880031849

Outcome results