Clinical Trials Directory

Trials / Completed

CompletedNCT06039137

The Effect of Switching the H1-antagonist Clemastine to Cetirizine in Premedication Regimens During Paclitaxel Treatment

The Effect of Switching the H1-antagonist Clemastine to Cetirizine in Premedication Regimens During Paclitaxel Treatment: 'The H1-SWITCH Study'

Status
Completed
Phase
Study type
Observational
Enrollment
395 (actual)
Sponsor
Erasmus Medical Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

In this study the effect of substituting clemastine IV to cetirizine PO on the occurence of hypersensitivity reactions during paclitaxel chemotherapy will be investigated.

Detailed description

This is a single arm before-after study with a historic control cohort to evaluate the effect of a policy change (i.e. substitution of clemastine IV for cetirizine PO) regarding the premedication scheme on the incidence of HSR during paclitaxel based chemotherapy.

Conditions

Interventions

TypeNameDescription
DRUGCetirizineSubjects were treated with a paclitaxel premedication regimen which contained oral cetirizine instead of intravenous clemastine
DRUGClemastine IVSubjects were treated with paclitaxel premedication containing clemastine 2 mg IV

Timeline

Start date
2022-06-01
Primary completion
2023-04-27
Completion
2023-10-31
First posted
2023-09-15
Last updated
2024-09-25

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT06039137. Inclusion in this directory is not an endorsement.

The Effect of Switching the H1-antagonist Clemastine to Cetirizine in Premedication Regimens During Paclitaxel Treatment (NCT06039137) · Clinical Trials Directory