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Clinical Trials/CTRI/2016/08/007210
CTRI/2016/08/007210RecruitingPhase 3

EFFECT OF STRUCTURED TEACHING MODULE ON INCIDENCE OF THE CAPECITABINE INDUCED HAND FOOT SYNDROME IN PATIENTS OF COLORECTAL CANCER AT TERTIARY CANCER CARE CENTRE A PROSPECTIVE RANDOMISED CONTROLLED STUDY

Tata Memorial Hospital0 sites280 target enrollmentStarted: TBDLast updated:
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Trial Snapshot

Phase
Phase 3
Status
Recruiting
Enrollment
280
Study OverviewEligibility CriteriaInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Observational

Eligibility Criteria

Inclusion Criteria

  • •patients above age of 18 yrs
  • •Planned for Capecitabine based chemotherapy for colorectal cancer in adjuvant or metastatic setting
  • •Can either read or write English, or Hindi or Marathi.
  • •Creatinine clearance > 60 ml/min
  • •Receiving capectabine in dose of 2000mg/m2/day

Exclusion Criteria

  • •Patients who are not willing to participate in the study
  • •patients with previous history of hand foot syndrome
  • •Previous exposure to 5-FU or Capecitabine < 1 year interval.
  • •Chemotherapy regimens which increase capecitabine induced toxicities e.g. irinotecan induced diarrhea requiring dose reduction of both Capecitabine and irinotecan.
  • •LFTs : AST/ALT > 3 ULN, bilirubin > 1.5 ULN, Albumin < 3.5

Investigators

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