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The Randomized Controlled Trial Study of the Incidence of Paclitaxel Hypersensitivity Reaction as First Line drug in Gynecologic Cancer Patients between 2 Steroid Premedication Type: Hydrocortisone & dexamethasone VS Dexamethasone alone

The Randomized Controlled Trial Study of the Incidence of Paclitaxel Hypersensitivity Reaction as First Line drug in Gynecologic Cancer Patients between 2 Steroid Premedication Type: Hydrocortisone & dexamethasone VS Dexamethasone alone

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
TCTR
Registry ID
TCTR20151122001
Enrollment
52
Registered
2015-11-22
Start date
2015-06-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gynecologic cancer patients who had not been received paclitaxel therapy. Hypersensitivity reaction Paclitaxel hypersensitivity reaction anaphylaxis Premedication Hydrocortisone Dexamethasone

Interventions

the nurses will record and report to doctor for management that following NCCN guideline. ,1.Hydrocortisone 100 mg&#44
dexamethasone 20 mg&#44
the nurses will record and report to doctor for management that following NCCN guideline.
Active Comparator Drug,Active Comparator Drug
Dexamethasone 20 mg intravenous,hydrocortisone 100 mg and dexamethasone intravenous
1. Dexamethasone 20 mg&#44
Ranitidine 50 mg&#44
Chlorpheniramine 10 mg intravenous 30 minutes before paclitaxel administration and other premedication including diphenhydramine 25 mg 2 capsule orally and Ondransetron 8 mg intravenously. 2. Patient
induced hypersensitivity reactions&#44
Oncology nursing forum. 4.If hypersensitivity reaction had occured&#44

Sponsors

none
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
25 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Gynecologic cancer patient who had pathology report 2.Need paclitaxel therapy 3.Patient who had not been received paclitaxel 4.Bone marrow, kidney,and liver were with in normal limit

Exclusion criteria

Exclusion criteria: 1.allergy to hydrocortisone 2.patient who had been received paclitaxel 3.patient who had history of paclitaxel allergy

Design outcomes

Primary

MeasureTime frame
Incidence of hypersensitivity reaction during intravenous paclitaxel infusion medical record about hypersensitivity reaction during intravenous paclitaxel infusion

Secondary

MeasureTime frame
none none none

Countries

Thailand

Contacts

Public ContactDhammapoj Jeerakornpassawat

Obstetrics and Gynaecology Department, Faculty of Medicine, Chiang Mai University

dhammapoj.zhou@gmail.com+66890431131

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026