Trial · NCT00066365
Registered outcomes12
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 12 of 12
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Status of FAS Ligand in Pre-chemotherapy Sample | 29 days after start of protocol therapy | FAS ligand (FASL) is a homotrimeric type II transmembrane protein expressed on cytotoxic T lymphocytes. The Cluster of Differentiation 1a (CD1a) status is measured in Immunohistochemistry (IHC) categories. |
| Primary | Presence of FAS in Pre-chemotherapy Sample | 29 days after start of protocol therapy | FAS/APO-1 is a transmembrane receptor. The presence is measured in Immunohistochemistry (IHC) categories. |
| Primary | FAS Ligand in Post Chemotherapy Sample | 29 days after start of protocol therapy | FAS ligand or FASL is a homotrimeric type II transmembrane protein expressed on cytotoxic T lymphocytes. The presence is measured in Immunohistochemistry (IHC) categories. |
| Primary | FAS Status in Post Chemotherapy Sample | 29 days after start of protocol therapy | FAS/APO-1 is a transmembrane receptor. The presence is measured in Immunohistochemistry (IHC) categories. |
| Primary | CD1a Status in Pre Chemotherapy Sample | 29 days after start of protocol therapy | CD1a (Cluster of Differentiation 1a) is a human protein encoded by the CD1A gene, presence is measured by positivity. |
| Primary | CD1a Status in Post Chemotherapy Sample | 29 days after start of protocol therapy | CD1a (Cluster of Differentiation 1a) is a human protein encoded by the CD1A gene, presence is measured by positivity. |
| Primary | S100 Status in Pre Chemotherapy Sample | 29 days after start of protocol therapy | The S-100 proteins are a family of low-molecular-weight proteins characterized by two calcium-binding sites that have helix-loop-helix ("EF-hand type") conformation. |
| Primary | S100 Status in Post Chemotherapy Sample | 29 days after start of protocol therapy | The S-100 proteins are a family of low-molecular-weight proteins characterized by two calcium-binding sites that have helix-loop-helix ("EF-hand type") conformation. |
| Primary | Clusterin Status in Pre Chemotherapy Sample | 29 days after start of protocol therapy | The protein encoded by this gene can under some stress conditions also be found in the cell cytosol. It has been suggested to be involved in several basic biological events such as cell death, tumor progression, and neurodegenerative disorders. |
| Primary | Clusterin Status in Post Chemotherapy Sample | 29 days after start of protocol therapy | |
| Primary | Event Free Survival (EFS) | Time of enrollment to Event or 5 years from enrollment, whichever occurs first | EFS defined as the time from enrollment on the study until disease progression, occurrence of a second malignant neoplasm (SMN), death or last contact, whichever comes first. Disease progression, occurrence of a SMN or death will be considered an analytic even. In all other cases, the patient will be considered censored at last contact. |
| Primary | Feasibility Success | Enrollment through 21 days of protocol therapy | Feasibility success defined as received 21 days of protocol therapy, did not experience grade III or grade IV toxicity according to Common Toxicity Criteria for Adverse Events (CTCAE) version 3 and rendered surgically free of disease in the lungs. |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
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GET https://conductscience.org/api/trials/v1/NCT00066365/registered