[96a5a0]: / output / allTrials / identified / NCT03270072_identified.json

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{
"info": {
"nct_id": "NCT03270072",
"official_title": "The Differential Impact of Proton Beam Irradiation Versus Conventional Radiation on Organs-at-risk in Stage II-III Breast Cancer Patients",
"inclusion_criteria": "* Eligible for and scheduled to receive radiation therapy on Radiation Therapy Oncology Group (RTOG) Trial 3510 (Pragmatic Phase III Randomized Trial of Proton vs Photon Therapy for Patients with Non-Metastatic Breast Cancer Receiving Comprehensive Nodal Radiation: A Radiotherapy Comparative Effectiveness (RADCOMP) Consortium Trial). (NCT02603341)\n* Ability to understand and the willingness to sign a study-specific written informed consent document\nHealthy volunteers allowed\nMust have minimum age of 21 Years",
"exclusion_criteria": "* There are no exclusion criteria.",
"miscellaneous_criteria": ""
},
"inclusion_lines": [
{
"line": "* Eligible for and scheduled to receive radiation therapy on Radiation Therapy Oncology Group (RTOG) Trial 3510 (Pragmatic Phase III Randomized Trial of Proton vs Photon Therapy for Patients with Non-Metastatic Breast Cancer Receiving Comprehensive Nodal Radiation: A Radiotherapy Comparative Effectiveness (RADCOMP) Consortium Trial). (NCT02603341)",
"criterions": [
{
"exact_snippets": "Eligible for and scheduled to receive radiation therapy on Radiation Therapy Oncology Group (RTOG) Trial 3510",
"criterion": "eligibility for RTOG Trial 3510",
"requirements": [
{
"requirement_type": "eligibility",
"expected_value": true
}
]
},
{
"exact_snippets": "scheduled to receive radiation therapy on Radiation Therapy Oncology Group (RTOG) Trial 3510",
"criterion": "scheduled to receive radiation therapy",
"requirements": [
{
"requirement_type": "scheduling",
"expected_value": true
}
]
}
]
},
{
"line": "* Ability to understand and the willingness to sign a study-specific written informed consent document",
"criterions": [
{
"exact_snippets": "Ability to understand",
"criterion": "understanding ability",
"requirements": [
{
"requirement_type": "presence",
"expected_value": true
}
]
},
{
"exact_snippets": "willingness to sign a study-specific written informed consent document",
"criterion": "willingness to sign consent",
"requirements": [
{
"requirement_type": "presence",
"expected_value": true
}
]
}
]
},
{
"line": "Healthy volunteers allowed",
"criterions": [
{
"exact_snippets": "Healthy volunteers allowed",
"criterion": "volunteer health status",
"requirements": [
{
"requirement_type": "status",
"expected_value": "healthy"
}
]
}
]
},
{
"line": "Must have minimum age of 21 Years",
"criterions": [
{
"exact_snippets": "minimum age of 21 Years",
"criterion": "age",
"requirements": [
{
"requirement_type": "minimum",
"expected_value": {
"operator": ">=",
"value": 21,
"unit": "Years"
}
}
]
}
]
}
],
"exclusion_lines": [
{
"line": "* There are no exclusion criteria.",
"criterions": [
{
"exact_snippets": "no exclusion criteria",
"criterion": "exclusion criteria",
"requirements": [
{
"requirement_type": "presence",
"expected_value": false
}
]
}
]
}
],
"miscellaneous_lines": [],
"failed_inclusion": [],
"failed_exclusion": [],
"failed_miscellaneous": []
}