Skip to content

A clinical trial to study the effectiveness of gavakshi moola decoction with milk in kamala (hepatocellular jaundice).

Clinical study to evaluate the effectiveness of Gavakshi moola (citrullus colocynthus) draava with ksheera in kamala (hepatocellular jaundice)

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/08/015390
Enrollment
30
Registered
2018-08-20
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: R17- Unspecified jaundice

Interventions

Intervention1: Gavakshi moola drava 6ml with 150 ml ksheera in empty stomach early morning for 3 days: Gavakshi moola drava 6ml with 150 ml ksheera in empty stomach early morning for 3 days Control In

Sponsors

Sri Dharmasthala Manjunatheshwara College of Ayurveda and Hospital hassan
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • Child-Turcotte-Pugh Score of 5-10 18 • Hepatocellular jaundice due to viral hepatitis, alcoholic liver disease • Subjects of either gender, between the age of 18 to 60 years . • Subjects who are ready to sign the informed consent form.

Exclusion criteria

Exclusion criteria: Serum Bilirubin levels above 10 mg/dL 19 Subjects with uncontrolled Diabetes mellitus, Malignant Hypertension Known cases of hepatic cancer, liver metastasis, Ca pancreas. Pregnant or lactating women

Design outcomes

Primary

MeasureTime frame
PRIMARY OUTCOME MEASURES: Subjective parameters : Netra peetata Twak peetata Peeta mootrata Sadana (anga glani) Daha Avipaka Aruchi Objectives parameters: Serum bilirubin Transaminases Albumin Globulin Ratio Timepoint: before treatment - baseline data after treatment - after 3 days of intervention

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDr Lakshmiprasad L Jadhav

Post graduate scholar

madhavirao551@gmail.com9480620992

Outcome results

None listed

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