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Role of Maharishi Amrit Kalash, Ayurvedic herbal medicine on Breast Cancer

Study of effectiveness of Maharishi Amrit Kalash on Breast Cancer as adjunct therapy along with Docetaxil and Epirubicine chemotherapy.

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/02/017775
Enrollment
160
Registered
2019-02-22
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: null- Breast Cancer

Interventions

Intervention1: MAK: MAK 4 MAK 5 Intervention2: MAK (MAK 4 and MAK 5): MAK 4 paste dose 2tsf twice a day with milk orally. MAK 5 dose 2tablets twice a day with luke warm water orally for a period of 5

Sponsors

Maharishi Ayurveda Products Pvt Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients who are willing to participate in the study. 2. Women between age18 and 70 years, with histopathologically confirmed breast carcinoma of maximum diameter equal to 2.1 cm or above in whom neoadjuvant chemotherapy is planned. 3.Patients with skin involvement with fixed nodal metastasis will also be included. 4.Patients signed written informed consent. 5.Patients with normal liver and renal function test and normal ECG and echocardiogram.

Exclusion criteria

Exclusion criteria: 1. Patients unwilling to participate. 2. Pregnant and lactating women. 3. Patients with concomitant severe heart, liver or renal diseases. 4. Patients with type one diabetes or uncontrolled type two diabetes with complications and/or on Insulin. 5.Patients deemed unfit to received chemotherapy due to poor general health

Design outcomes

Primary

MeasureTime frame
Complete regression of tumor (clinical and pathological) in patients with breast cancer during neo-adjuvant chemotherapy.Timepoint: Clinical regression at each chemotherapy cycle (3 weekly) intervals. Pathological regression after surgery (app 6 months).

Secondary

MeasureTime frame
Reduction of chemo toxicity in patients with breast cancer.Timepoint: After each chemotherapy cycle

Countries

India

Contacts

Public ContactDr Anurag Srivastava

All India Institute of Medical Sciences New Delhi INDIA

dr.anuragsrivastava@gmail.com09868397729

Outcome results

None listed

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