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Safety and Feasibility of the EasyfyCare digital Platform aims to streamline the treatment process and for safer administration of chemotherapy closer to participants home.

A Prospective Multicentre Observational Study to Evaluate the safety, feasibility and Health Economic Impact of the EasyfyCare Software -as-a-Service Platform in Decentralised Chemotherapy Administration - EASY-CHEMO

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/101327
Enrollment
50
Registered
2026-01-16
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: X- New Technology

Interventions

Intervention1: Nil: Nil

Sponsors

EasyfyHealthcare Pvt Ltd,
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Histologically confirmed malignancy Planned intravenous chemotherapy suitable for decentralised administration ECOG performance status 0-2 Ability to provide informed consent

Exclusion criteria

Exclusion criteria: High risk Chemotherapy requiring ICU level monitoring Chemotherapy protocol involving consecutive days chemo Unstable comorbid conditions Patients unwilling or unable to comply with digital followup

Design outcomes

Primary

MeasureTime frame
Incidence of chemotherapy related Grade , Proportion of planned Chemotherapy cycles completed using EasyfyCare,Proportion of cases with complete digital workflow documentationTimepoint: The primary outcome was assessed over a six months study period

Secondary

MeasureTime frame
Acceptance of EasyfyCare (Patient, nurse & clinician satisfaction scores), Time Saved (Reduction in travel time & hospital visits, Cost Savings( reduction in out of pocket expenditure like travel accomadation,wageloss),Dropouts(Chemotherapy discontinuation & loss to follow up rates),Supportive Care Utilisation( Number of unplanned emergency visits or hospital admissions)Timepoint: The secondary outcome was assessed over a six months time period

Countries

India

Contacts

Public ContactKavitha VC

MVR Cancer Centre and Research Institute

drnkwarrier@mvrccri.co9495617585

Outcome results

None listed

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