TO ASSESS THE EFFECT OF DHANYAKA HIMA AND KUNJALA KRIYA IN AMLAPITTA(ACIDITY)

â??A RANDOMIZED COMPARATIVE CLINICAL TRIAL TO ASSESS THE â??AMLAPITTAHARAâ??EFFECT OF DHANYAKA HIMA AND KUNJALA KRIYAâ??

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2018/12/016765

Enrollment

Registered

2018-12-21

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

Health Condition 1: K318- Other specified diseases of stomach and duodenum

Interventions

Intervention1: GROUP A- DHANYAKA HIMA: 30 clinically diagnosed and registered patients of Amlapitta will be treated by Dhanyaka Hima. Yavkut of Dhanyaka will be allowed to soak in 6 times water (16 gm

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients having classical symptoms of Amlapitta and symptoms of Urdhvaga Amlapitta. 2.Patients of either sex and between 18-60 years of age. 3.Patients willing and able to carry out treatment for 4 weeks. 4.Patients will be registered with duly signed informed consent prior to the trial.

Exclusion criteria

Exclusion criteria: 1.Patients with diagnosed cases of gastric, peptic and duodenal ulcers. 2.Patients with any GIT, abdominal complications and chronic illness. 3.Patients with diagnosed cases of any systemic disorder. 4.Pregnant and lactating women.

Design outcomes

Primary

Measure	Time frame
TO assess the improvement in subjective parameter i.e. signs & symptoms of Amlapitta.Timepoint: 4 weeks for each patients.	—

Secondary

Measure	Time frame
TO assess the improvement in subjective parameter i.e. signs & symptoms of Amlapitta.Timepoint: 4 weeks for each patients.	—

Countries

India

Contacts

Public ContactDR SARVESH KUMAR AGRAWAL

NATIONAL INSTITUTE OF AYURVEDA,

kksayu@gmail.com9413345633

Outcome results

None listed

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