MedPath

Study of the excess cost associated with the drug wasted due to limited options of the size of anti-cancer drug vials, among patients receiving such treatment at Tata Memorial Hospital

Not Applicable
Conditions
Health Condition 1: C00-D49- Neoplasms
Registration Number
CTRI/2020/08/027054
Lead Sponsor
ot Applicable
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Adult cancer patients

The patients advised and receiving any of the following 62 chemotherapy protocols will be included in the study.

Solid 1

AC

Paclitaxel+-trastuzumab

Gemcitabine+carboplatin

EC

TDM1

CMF

Carboplatin+paclitaxel+/-Bevacizumab

Liposomal doxorubin

TCH(Docetaxel,carboplatin,trastuzumab)

BEP

EP

EMACO

EMA EP

SA Dactinomycin

SA Methotrexate

mFOLFOX

FOLFIRI

Cape-OX

Cap-Irinotecan

SA Docetaxel

Cetuximab

Panitumumab

Trastuzumab

Ramucirumab

Cape-Mitomycin

FOLFIRINOX

Gem-Oxaliplatin

Gem+cisplatin

DOF

EOX

DCF

Gem+nab paclitaxel

Solid 2

Pemetrexed+Cisplatin

Pemetrexed+Carboplatin

Pemetrexed-carboplatin+/- pembrolizumab

Gemcitabine+carboplatin

Paclitaxel+carboplatin

Geftinib+bevacizumab

Nivolumab

Cisplatin+etoposide

Carboplatin+etoposide

SA Irinotecan

SA Gemcitabine

SA Paclitaxel

SA Docetaxel

BEP

EP

Gemcitabine+cisplatin

Gemcitabine+carboplatin

TIP

Adult Hematology

VCD

VRD

RDHAP

RGDP

RCHOP

ABVD

Bendamustine-rituximab

FCR

R EPOCH

HiDAC

CHOP

RCEOP

Exclusion Criteria

patients aged < 18 years

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath