Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorInstituto Nacional de Cancerologia de Mexico
About this trial
This study evaluate the association of body composition (mainly free-fat mass), clinical and biochemical parameters with development of toxicity in patients under treatment with Carboplatin/Paclitaxel in advanced NSCLC.
Eligibility criteria
Qualifiers
Diagnosis of NSCLC Stage IV (stratification according to the American Joint Committee on Cancers - 7th edition)
Candidates for treatment with carboplatin plus paclitaxel 1st line
Performance status (ECOG 0-2)
Laboratory studies that demonstrate adequate renal, hepatic and hematologic function (blood chemistry and blood count)
Disqualifiers
Patients with renal impairment (KDOQI 3-5)
Patients who do not have computed tomography study at baseline
Uncontrolled blood pressure (> 140 mmHg)
Uncontrolled diabetes (> 130 mg / dL)
Trial design
Treatments tested in this trial
- Carboplatin
Treatment groups
132 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov