Skip to content

The effect of Swastha Thriphala, an Ayurveda medicinal formulation on side-effects of therapy and quality of life in cancer patients

The effects of a herbal medicinal product, Swastha Thriphala, on the side effects of chemotherapy and radiotherapy in patients with cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
SLCTR
Registry ID
SLCTR/2013/036
Enrollment
200
Registered
2013-11-29
Start date
2013-12-30
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Side effects of chemotherapy and radiotherapy in cancer

Interventions

Participants will be randomized into two arms. The intervention arm will receive Swastha Thriphala 750g to be taken orally twice daily for 30 days. The control arm will receive a standardized placeb

Sponsors

Link Natural Products (Pvt) Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Consenting adults 20-70 years 2. With any diagnosed cancer 3. Receiving chemotherapy or radiotherapy (intervention will be given concomitantly with the chemotherapy/radiotherapy regimens) for cancer 4. Presenting to the Oncology Clinic Teaching Hospital Karapitiya, Galle.

Exclusion criteria

Exclusion criteria: Patients with diagnosed 1. Heart failure 2. Chronic kidney diseases 3. Respiratory diseases 4. Chronic liver diseases 5. Stroke 6. Dementia 7. Frailty 8. Parkinson disease

Design outcomes

Primary

MeasureTime frame
Haematological side effects (changes in neutrophil count, haemoglobin and platelets) [Baseline, 3 days, 7 days, 14 days and 30 days of treatment] Patient assessment of fatigue, sleep and hair loss [Baseline, 3 days, 7 days, 14 days and 30 days of treatment]

Secondary

MeasureTime frame
None [None]

Countries

Sri Lanka

Contacts

Public ContactProfessor Colvin Goonaratna

Registrar

si7np5e@gmail.com4 612 643

Outcome results

None listed

Source: SLCTR (via WHO ICTRP) · Data processed: Aug 9, 2026