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Paclitaxel allergic reactio

Phase 3
Conditions
Health Condition 1: C00-D49- Neoplasms
Registration Number
CTRI/2021/07/034839
Lead Sponsor
CI AIIMS
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

Adults patients with age between 18 years to 70 years

Histopathological diagnosis of cancer

Willing to participate and to give written informed consent

Naïve to conventional paclitaxel chemotherapy and planned to receive conventional paclitaxel either as single agent or in combination

ECOG performance status 0-2

Stable baseline vital signs: Afebrile, radial artery blood pressure (90/60 â?? 130/90mm Hg), pulse rate 60 â?? 100 / minutes, respiratory rate 12-18/ minutes, 97.8 °F to 99.1 °F (36.5° C to 37.3° C);

Exclusion Criteria

Past history of hypersensitivity reaction to paclitaxel or cremophor containing drugs (cyclosporine, propofol, diazepam, teniposide, etoposide, Vitamin K) or partner drug or pheniramine or ranitidine

On chronic systemic steroids or received any dose in the last week

No history of hypersensitivity to partner drug

Hb < 8gm/dl, ANC < 1000/m3, creatinine > 2mg/dl, Bilirubin > 5 X ULN, transaminases 10 times or more

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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