Bioelectrical Impedance Phase Angle in Predicting Treatment Outcome in Patients With Extensive Stage Small Cell Lung Cancer Receiving First-Line Chemotherapy
This clinical trial studies bioelectrical impedance phase angle in predicting treatment outcome in patients with extensive stage small cell lung cancer receiving first-line chemotherapy. Diagnostic procedures, such as bioelectrical impedance analysis, may help predict a patient's response to treatment for small cell lung cancer.
Checked against the public recordLast updated Jul 5, 2018 · Source: ClinicalTrials.gov
What this study is about
- Purpose
- Diagnostic
- Study type
- Interventional
- Phase
- Not applicable
- Sponsor
- Wake Forest University Health Sciences
- Interventions being studied
- Procedure: bioelectric impedance analysis
How this study is categorized
These labels come from structured fields and exact terms in the public record.
Who may be able to participate
Inclusion Criteria: * A primary histopathological and/or cytopathological diagnosis of small cell lung cancer (SCLC) * Diagnosis of extensive stage disease (extensive stage \[ES\]-SCLC), with stage established by computed tomography (CT), magnetic resonance imaging (MRI), or positron emission tomography (PET) scan * Scheduled to receive front-line platinum-based chemotherapy with carboplatin or cisplatin plus etoposide * Ability to understand and the willingness to sign an institutional review board (IRB)-approved informed consent document Exclusion Criteria: * No recent chemotherapy or surgery, as defined as in the last 6 months * Presence of a pacemaker or defibrillator * Patients with major chronic disease known to adversely affect PA, including human immunodeficiency virus (HIV)/acquired immune deficiency syndrome (AIDS), congestive heart failure, tuberculosis * Patients with body mass index (BMI) greater than 34 or less than 16 * Any condition or abnormality which may, in the opinion of the investigator, compromise the safety of patients * Unable or unwilling to follow protocol requirements * Pregnant women are excluded from participation due to inability to participate in required chemotherapy regimen
Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.
U.S. locations
- Comprehensive Cancer Center of Wake Forest UniversityWinston-Salem, North Carolina
Source and freshness
Processed from ClinicalTrials.gov. Last public update: Jul 5, 2018. Always confirm current availability with the study team.