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S1013: Validation of Cancer Questionnaire for Skin Toxicities in Patients With Colorectal Cancer or Lung Cancer Receiving Cetuximab, Panitumumab, or Erlotinib Hydrochloride
NCT01416688 · View on ClinicalTrials.gov ↗
Study Summary
RATIONALE: Questionnaires that patients can use to assess skin toxicities related to treatment may help identify the intermediate-and long-term effects of cetuximab, panitumumab, or erlotinib hydrochloride. PURPOSE: This trial studies the validation of a cancer questionnaire for skin toxicities in patients with colorectal or lung cancer receiving cetuximab, panitumumab, or erlotinib hydrochloride.
Conditions Studied
Interventions
- PROCEDURE quality-of-life assessment
- PROCEDURE psychosocial assessment and care
- PROCEDURE assessment of therapy complications
Study Locations (20)
California
- East Bay Radiation Oncology Center — Castro Valley
- City of Hope Comprehensive Cancer Center — Duarte
- Epic Care-Dublin — Dublin
- Bay Area Breast Surgeons Inc — Emeryville
- Epic Care Partners in Cancer Care — Emeryville
- UC San Diego Moores Cancer Center — La Jolla
- Loma Linda University Medical Center — Loma Linda
- Los Angeles County-USC Medical Center — Los Angeles
- USC / Norris Comprehensive Cancer Center — Los Angeles
- Contra Costa Regional Medical Center — Martinez
- El Camino Hospital — Mountain View
- Highland General Hospital — Oakland
- Alta Bates Summit Medical Center - Summit Campus — Oakland
- Bay Area Tumor Institute — Oakland
- Hematology and Oncology Associates-Oakland — Oakland
- Doctors Medical Center- JC Robinson Regional Cancer Center — San Pablo
Arizona
- University of Arizona Cancer Center-North Campus — Tucson
- The University of Arizona Medical Center-University Campus — Tucson
Illinois
- Saint Joseph Medical Center — Bloomington
- Illinois CancerCare-Bloomington — Bloomington
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 146 participants |
| Start Date | 2011-11-15 |
| Est. Completion | 2019-04-08 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01416688
The ClinicalTrials.gov registry entry for NCT01416688 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 146 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is SWOG Cancer Research Network, which has 212 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 4 conditions, with Lung Cancer appearing as the primary indexed condition, and to 3 interventions — of which quality-of-life assessment is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT01416688 reports 20 study locations spanning 3 distinct geographic areas — top geographies include California, Arizona, Illinois. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT01416688 about?
NCT01416688 is a clinical study titled "S1013: Validation of Cancer Questionnaire for Skin Toxicities in Patients With Colorectal Cancer or Lung Cancer Receiving Cetuximab, Panitumumab, or Erlotinib Hydrochloride". RATIONALE: Questionnaires that patients can use to assess skin toxicities related to treatment may help identify the intermediate-and long-term effects of cetuximab, panitumumab, or erlotinib hydrochloride. PURPOSE: This trial studies the validation of a cancer questionnaire for skin toxicities in ...
What is the current status of trial NCT01416688?
This trial is currently completed. The enrollment target is 146 participants. The study started on 2011-11-15. Estimated completion is 2019-04-08.
What conditions does trial NCT01416688 study?
This clinical trial studies the following conditions: Lung Cancer, Colorectal Cancer, Dermatologic Complications, Therapy-related Toxicity. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT01416688?
The interventions under investigation include: quality-of-life assessment (PROCEDURE), psychosocial assessment and care (PROCEDURE), assessment of therapy complications (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT01416688?
This trial is sponsored by SWOG Cancer Research Network, which has 212 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT01416688 being conducted?
This trial has 20 study locations across Arizona, California, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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