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Evaluation of role of Ayurvedic Management in Chemotherapy-induced Peripheral Neuropathy in cancer patients

Evaluation of role of Ayurvedic Management in Chemotherapy-induced Peripheral Neuropathy in cancer patients - an open labeled randomized control clinical trial. - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/100454
Enrollment
105
Registered
2026-01-07
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: G620- Drug-induced polyneuropathy

Interventions

None listed

Sponsors

Bharatiya Sanskriti Darshan Trusts Integrated Cancer Treatment and Research Centre
Lead Sponsor
Dr Anjali Deshpande PhD Guide Professor and HOD Dept of Kayachikitsa
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Histologically confirmed cancer patients, irrespective of stage of cancer, undergoing Taxane or Platinum-based chemotherapy, or within 2 years after completion of this protocol and has clinical diagnosis of CIPN of grade 1 to 3 according to NCI-CTC version 4.03

Exclusion criteria

Exclusion criteria: 1. Patient having a history of peripheral neuropathy unrelated to chemotherapy, such as diabetic neuropathy, severe renal failure, liver impairment and alcoholism. 2. Brain and central nervous system metastases. 3. Known conditions such as auto-immune diseases, infections, bone / joint diseases causing injury or pressure on the nerve, exposure to poisons, and low vitamin levels.

Design outcomes

Primary

MeasureTime frame
To assess the efficacy of Ayurvedic treatment in managing symptoms of CIPN and improving QoL of cancer patients.Timepoint: To assess the efficacy of Ayurvedic treatment in managing symptoms of CIPN and improving QoL of cancer patients.

Secondary

MeasureTime frame
To evaluate the efficacy of Ayurvedic treatment in patients with CIPN by electrodiagnostic parameters i.e Nerve Conduction Velocity (NCV) test.Timepoint: Nerve Conduction Velocity (NCV) test will be done at time point namely baseline (A), 3 months (B), 6 months (C) and 1 year (E) after enrolment in all the groups.

Countries

India

Contacts

Public ContactDr Anjali Aniruddha Deshpande

Bharatiya Sanskriti Darshan Trusts Integrated Cancer Treatment and Research Centre

ictrcpune@gmail.com9820648058

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026