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A study on the influence of blood levels of drugs -Adriamycin, Cyclophosphamide and Paclitaxel on the health condition of patients with breast cancer in a medical college hospital

A study on the influence of plasma concentrations of Adriamycin, Cyclophosphamide and Paclitaxel on clinical outcome of patients with breast cancer in a tertiary care hospital

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2017/06/008766
Enrollment
30
Registered
2017-06-06
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: C50- Malignant neoplasm of breast

Interventions

None listed

Sponsors

M S Yamuna devi
Lead Sponsor
K Bhuvaneswari
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1.All Ca breast patients on AC/T regimen â??diagnosed based on AJCC staging criteria, belonging to Stage I, Stage II, Stage III 2.All these 3 groups with laboratory parameters between normal limit to upper limit of contraindicated values

Exclusion criteria

Exclusion criteria: 1.Patients who were on other chemotherapy regimens previously 2.Tumor beyond stage IV 3.Patients with co morbid conditions like renal failure, liver failure and cardiac problems

Design outcomes

Primary

MeasureTime frame
abnormalities in the liver and renal function tests (less than the lower limit or more than the upper limit of normal)correlated with the plasma concentrations of Adriamycin, Cyclophosphamide and Paclitaxel analysed through HPLCTimepoint: at the third cycle of AC/T regimen

Secondary

MeasureTime frame
clinical reduction (%) in tumour size correlated with the plasma concentrations of Adriamycin, Cyclophosphamide and Paclitaxel analysed through HPLCTimepoint: at the third cycle of AC/T regimen;corelation of estrogen and progesterone receptors with plasma concentrations of Adriamycin, Cyclophosphamide and Paclitaxel and related ADRs in patients with Ca breast Timepoint: at the third cycle of AC/T regimen

Countries

India

Contacts

Public ContactM S Yamuna devi

PSG Institute of Medical Sciences and Research

nandabhuvana@gmail.com9894769934

Outcome results

None listed

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