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Anti nausea treatment based on individual genetic alterations (SNP) and simultaneous test of the validity of acupressure in conjuction with chemotherapy in women with breast cancer.

Phase 1
Conditions
ausea in conjuction with neoadjuvant or adjuvant chemotherapy (FEC/EC) for patients with breast cancer.
Therapeutic area: Diseases [C] - Cancer [C04]
Registration Number
EUCTR2015-000658-39-SE
Lead Sponsor
Region Jönköpings län
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
All
Target Recruitment
840
Inclusion Criteria

Until 31 Dec 2020: Women with verified breast cancer planed for first neoadjuvant or adjuvant FEC/EC chemotherapy an
Age = 18 years
From 2021:
Patients with a cancer diagnosis that are planned for potentially emetogenic chemotherapy
Knowledge of the Swedish language
Informed consent in writing
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 590
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 250

Exclusion Criteria

? Distant metastases in patients treated in an adjuvant setting
? Previous treatment with chemotherapy
? Unable to understand information about the study
Only until 31 Dec 2020: Contra indication against betamethasone

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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