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Estimation of the bicarbonate difference under optimal and real conditions in the neoadjuvant treatment of early breast cancer

Estimation of the bicarbonate difference under optimal and real conditions in the neoadjuvant treatment of early breast cancer - Your time

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00033577
Enrollment
30
Registered
2024-02-07
Start date
2024-03-01
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

C50.9

Interventions

Group 1: patients with early breast cancer who underwent neoadjuvant chemotherapy at Dept. of Ob/Gyn of University Hospital Ulm.

Sponsors

Klinik für Frauenheilkunde und Geburtshilfe, Universitätsklinikum Ulm
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients who receive neoadjuvant treatment of an eBC in the Ulm Women's Clinic during the defined recruitment interval.

Exclusion criteria

Exclusion criteria: The exclusion criteria are recurrence and/or metastatic disease.

Design outcomes

Primary

MeasureTime frame
A questionnaire is used to evaluate the quality of life. Additionally, the time that the patient spent during neoadjuvant period with her treatment (chemotherapy and additional visits) will be recorded in order to discover the potential for optimization.

Secondary

MeasureTime frame
The carbon-footprint of the therapy will be calculated based on the time spent in the therapy and other factors.

Countries

Germany

Contacts

Public ContactStefan Lukac

Klinik für Frauenheilkunde und Geburtshilfe, Universitätsklinikum Ulm

stefan.lukac@uniklinik-ulm.de+4973150088

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026