Health Condition 1: C33- Malignant neoplasm of trachea
Conditions
Interventions
Intervention1: NIL: NIL
Control Intervention1: NIL: NIL
Sponsors
Nil
Eligibility
Inclusion criteria
Inclusion criteria: 1) Adult patients with a diagnosis of cancer >=60 years of age. 2) Patients willing to sign the informed consent form.
Exclusion criteria
Exclusion criteria: History of hypersensitivity to active ingredient Tc-DTPA
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The objective of the present study is to compare methods for GRF estimation where the methods will be compared using a Bland-Altman plot.Timepoint: As the study duration is fixed for 2 years the primary outcome will be assessed by capturing data inclusive of demographic parameters such as age, height, weight and laboratory parameters such as serum creatinine, albumin and serum cystatin levels to be incorporated in the GFR estimating equations. These parameters will be captured at a one time visit within the study duration. | — |
Secondary
| Measure | Time frame |
|---|---|
| NILTimepoint: NIL | — |
Countries
India
Contacts
Public ContactDr Vikram Gota
Advanced Centre for Treatment, Research and Education in Cancer (ACTREC)
Outcome results
None listed