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
| Type | Name | Description |
|---|---|---|
| DRUG | Cetirizine | Subjects were treated with a paclitaxel premedication regimen which contained oral cetirizine instead of intravenous clemastine |
| DRUG | Clemastine IV | Subjects 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.