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12 Weeks Intervention of Body Revival in Breast Cancer Patients

12-week Intervention of Body Revival (Ayurvedie Medicine) to Improve Quality of Life (QoL) and Progression Free Survival (PFS) to Counter Adverse Events of Chemotherapy or Radiotherapy in Post Surgery Breast Cancer Patients: A Randomized Case Control Study - BC

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/11/059465
Enrollment
48
Registered
2023-11-02
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Health Condition 1: C509- Malignant neoplasm of breast of unspecified site Health Condition 2: O- Medical and Surgical

Interventions

None listed

Sponsors

Health Reactive
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 18 years of age or older; With a histologically or cytologically confirmed diagnosis of breast cancer (stage II–IV); Have been treated with surgery / first line chemotherapy / radiotherapy of not more than six months Not relapsed during recruitment Subjects may not have received Body Revival® or any herbal medicine

Exclusion criteria

Exclusion criteria: Clinically significant CNS, hepatic, cardio-respiratory or immunogenic problems;Pregnant woman and lactating mother; Subjects have received Body Revival® or any herbal medicine

Design outcomes

Primary

MeasureTime frame
(a) Progression free survival by blood CA-15.3, (b) Quality o Life by Questionnaire for cancer patients and (c) Karnofsky Performances (clinical assessments) are the primary outcomes by comparison between Intervention vs. case matched control (without intervention)Timepoint: 1 year

Secondary

MeasureTime frame
(a) Progression free survival by blood CA-15.3, (b) Quality o Life by Questionnaire for cancer patients & (c) Karnofsky Performances (clinical assessments) are the primary outcomes by comparison between Intervention vs. case matched control (without intervention)Timepoint: 12 weeks

Countries

India

Contacts

Public ContactUtpalendu Jana

J B Roy State Ayurvedic Medical College and Hospital Kolkata

biswastuhin@rediffmail.com9748664647

Outcome results

None listed

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