[96a5a0]: / output / allTrials / logical / NCT03892720_logical.json

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{
"info": {
"nct_id": "NCT03892720",
"official_title": "A Phase II Study of Non-Coplanar SBRT Re-Irradiation Using HyperArc in Patients With Recurrent Head and Neck Cancer",
"inclusion_criteria": "* Histologically confirmed recurrent head and neck cancer; either unresectable or status post salvage surgery.\n* History of radiation therapy for head and neck cancer with minimum 50% overlap of the 50% isodose line from prior treatment to the proposed treatment volume.\n* Estimated life expectancy > 12 weeks.\n* Karnofsky performance status >= 70 (Eastern Cooperative Oncology Group [ECOG] 0-2).\n* Maximum tumor, or tumor bed, diameter < 5 cm.\n* If a woman is of childbearing potential, a negative serum pregnancy test must be documented. Women of childbearing potential must agree to use adequate contraception (hormonal or barrier method of birth control; or abstinence) for duration of study participation and for up to 4 weeks following the study treatment.\n* Ability to understand and willingness to sign a written informed consent.\nHealthy volunteers allowed\nMust have minimum age of 18 Years",
"exclusion_criteria": "",
"miscellaneous_criteria": ""
},
"inclusion_lines": [
{
"identified_line": {
"line": "* History of radiation therapy for head and neck cancer with minimum 50% overlap of the 50% isodose line from prior treatment to the proposed treatment volume.",
"criterions": [
{
"exact_snippets": "History of radiation therapy for head and neck cancer",
"criterion": "radiation therapy history",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "minimum 50% overlap of the 50% isodose line from prior treatment to the proposed treatment volume",
"criterion": "isodose line overlap",
"requirement": {
"requirement_type": "percentage overlap",
"expected_value": {
"operator": ">=",
"value": 50,
"unit": "%"
}
}
}
]
},
"logical_structure": {
"and_criteria": [
{
"exact_snippets": "History of radiation therapy for head and neck cancer",
"criterion": "radiation therapy history",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "minimum 50% overlap of the 50% isodose line from prior treatment to the proposed treatment volume",
"criterion": "isodose line overlap",
"requirement": {
"requirement_type": "percentage overlap",
"expected_value": {
"operator": ">=",
"value": 50,
"unit": "%"
}
}
}
]
}
},
{
"identified_line": {
"line": "* Estimated life expectancy > 12 weeks.",
"criterions": [
{
"exact_snippets": "Estimated life expectancy > 12 weeks.",
"criterion": "life expectancy",
"requirement": {
"requirement_type": "duration",
"expected_value": {
"operator": ">",
"value": 12,
"unit": "weeks"
}
}
}
]
},
"logical_structure": {
"and_criteria": [
{
"exact_snippets": "Estimated life expectancy > 12 weeks.",
"criterion": "life expectancy",
"requirement": {
"requirement_type": "duration",
"expected_value": {
"operator": ">",
"value": 12,
"unit": "weeks"
}
}
}
]
}
},
{
"identified_line": {
"line": "* Karnofsky performance status >= 70 (Eastern Cooperative Oncology Group [ECOG] 0-2).",
"criterions": [
{
"exact_snippets": "Karnofsky performance status >= 70",
"criterion": "Karnofsky performance status",
"requirement": {
"requirement_type": "score",
"expected_value": {
"operator": ">=",
"value": 70,
"unit": "N/A"
}
}
},
{
"exact_snippets": "Eastern Cooperative Oncology Group [ECOG] 0-2",
"criterion": "Eastern Cooperative Oncology Group (ECOG) performance status",
"requirement": {
"requirement_type": "score",
"expected_value": {
"comparisons": [
{
"operator": ">=",
"value": 0,
"unit": "N/A"
},
{
"operator": "<=",
"value": 2,
"unit": "N/A"
}
]
}
}
}
]
},
"logical_structure": {
"and_criteria": [
{
"exact_snippets": "Karnofsky performance status >= 70",
"criterion": "Karnofsky performance status",
"requirement": {
"requirement_type": "score",
"expected_value": {
"operator": ">=",
"value": 70,
"unit": "N/A"
}
}
},
{
"exact_snippets": "Eastern Cooperative Oncology Group [ECOG] 0-2",
"criterion": "Eastern Cooperative Oncology Group (ECOG) performance status",
"requirement": {
"requirement_type": "score",
"expected_value": {
"comparisons": [
{
"operator": ">=",
"value": 0,
"unit": "N/A"
},
{
"operator": "<=",
"value": 2,
"unit": "N/A"
}
]
}
}
}
]
}
},
{
"identified_line": {
"line": "* Maximum tumor, or tumor bed, diameter < 5 cm.",
"criterions": [
{
"exact_snippets": "Maximum tumor, or tumor bed, diameter < 5 cm.",
"criterion": "tumor or tumor bed diameter",
"requirement": {
"requirement_type": "size",
"expected_value": {
"operator": "<",
"value": 5,
"unit": "cm"
}
}
}
]
},
"logical_structure": {
"and_criteria": [
{
"exact_snippets": "Maximum tumor, or tumor bed, diameter < 5 cm.",
"criterion": "tumor or tumor bed diameter",
"requirement": {
"requirement_type": "size",
"expected_value": {
"operator": "<",
"value": 5,
"unit": "cm"
}
}
}
]
}
},
{
"identified_line": {
"line": "* If a woman is of childbearing potential, a negative serum pregnancy test must be documented. Women of childbearing potential must agree to use adequate contraception (hormonal or barrier method of birth control; or abstinence) for duration of study participation and for up to 4 weeks following the study treatment.",
"criterions": [
{
"exact_snippets": "If a woman is of childbearing potential",
"criterion": "childbearing potential",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "a negative serum pregnancy test must be documented",
"criterion": "serum pregnancy test",
"requirement": {
"requirement_type": "result",
"expected_value": "negative"
}
},
{
"exact_snippets": "Women of childbearing potential must agree to use adequate contraception (hormonal or barrier method of birth control; or abstinence)",
"criterion": "contraception use",
"requirement": {
"requirement_type": "agreement",
"expected_value": true
}
},
{
"exact_snippets": "Women of childbearing potential must agree to use adequate contraception (hormonal or barrier method of birth control; or abstinence)",
"criterion": "contraception use",
"requirement": {
"requirement_type": "method",
"expected_value": [
"hormonal",
"barrier",
"abstinence"
]
}
},
{
"exact_snippets": "for duration of study participation and for up to 4 weeks following the study treatment",
"criterion": "contraception duration",
"requirement": {
"requirement_type": "duration",
"expected_value": "for duration of study participation and for up to 4 weeks following the study treatment"
}
}
]
},
"logical_structure": {
"condition": {
"exact_snippets": "If a woman is of childbearing potential",
"criterion": "childbearing potential",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
"then_criteria": {
"and_criteria": [
{
"exact_snippets": "a negative serum pregnancy test must be documented",
"criterion": "serum pregnancy test",
"requirement": {
"requirement_type": "result",
"expected_value": "negative"
}
},
{
"and_criteria": [
{
"exact_snippets": "Women of childbearing potential must agree to use adequate contraception (hormonal or barrier method of birth control; or abstinence)",
"criterion": "contraception use",
"requirement": {
"requirement_type": "agreement",
"expected_value": true
}
},
{
"exact_snippets": "Women of childbearing potential must agree to use adequate contraception (hormonal or barrier method of birth control; or abstinence)",
"criterion": "contraception use",
"requirement": {
"requirement_type": "method",
"expected_value": [
"hormonal",
"barrier",
"abstinence"
]
}
},
{
"exact_snippets": "for duration of study participation and for up to 4 weeks following the study treatment",
"criterion": "contraception duration",
"requirement": {
"requirement_type": "duration",
"expected_value": "for duration of study participation and for up to 4 weeks following the study treatment"
}
}
]
}
]
},
"else_criteria": null
}
},
{
"identified_line": {
"line": "* Ability to understand and willingness to sign a written informed consent.",
"criterions": [
{
"exact_snippets": "Ability to understand",
"criterion": "cognitive ability",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "willingness to sign a written informed consent",
"criterion": "willingness to consent",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
}
]
},
"logical_structure": {
"and_criteria": [
{
"exact_snippets": "Ability to understand",
"criterion": "cognitive ability",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "willingness to sign a written informed consent",
"criterion": "willingness to consent",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
}
]
}
},
{
"identified_line": {
"line": "Healthy volunteers allowed",
"criterions": [
{
"exact_snippets": "Healthy volunteers allowed",
"criterion": "volunteer health status",
"requirement": {
"requirement_type": "status",
"expected_value": "healthy"
}
}
]
},
"logical_structure": {
"and_criteria": [
{
"exact_snippets": "Healthy volunteers allowed",
"criterion": "volunteer health status",
"requirement": {
"requirement_type": "status",
"expected_value": "healthy"
}
}
]
}
}
],
"exclusion_lines": [],
"miscellaneous_lines": [],
"failed_inclusion": [
{
"identified_line": {
"line": "* Histologically confirmed recurrent head and neck cancer; either unresectable or status post salvage surgery.",
"criterions": [
{
"exact_snippets": "Histologically confirmed recurrent head and neck cancer",
"criterion": "recurrent head and neck cancer",
"requirement": {
"requirement_type": "confirmation method",
"expected_value": "histologically confirmed"
}
},
{
"exact_snippets": "either unresectable or status post salvage surgery",
"criterion": "head and neck cancer resectability",
"requirement": {
"requirement_type": "resectability status",
"expected_value": [
"unresectable",
"status post salvage surgery"
]
}
}
]
},
"logical_structure": {
"and_criteria": [
{
"exact_snippets": "Histologically confirmed recurrent head and neck cancer",
"criterion": "recurrent head and neck cancer",
"requirement": {
"requirement_type": "confirmation method",
"expected_value": "histologically confirmed"
}
},
{
"or_criteria": [
{
"exact_snippets": "either unresectable or status post salvage surgery",
"criterion": "head and neck cancer resectability",
"requirement": {
"requirement_type": "resectability status",
"expected_value": "unresectable"
}
},
{
"exact_snippets": "either unresectable or status post salvage surgery",
"criterion": "head and neck cancer resectability",
"requirement": {
"requirement_type": "resectability status",
"expected_value": "status post salvage surgery"
}
}
]
}
]
}
},
{
"identified_line": {
"line": "Must have minimum age of 18 Years",
"criterions": [
{
"exact_snippets": "minimum age of 18 Years",
"criterion": "age",
"requirement": {
"requirement_type": "minimum",
"expected_value": {
"operator": ">=",
"value": 18,
"unit": "Years"
}
}
}
]
},
"logical_structure": {
"exact_snippets": "failed",
"criterion": "failed",
"requirement": {
"requirement_type": "failed",
"expected_value": "failed"
}
}
}
],
"failed_exclusion": [],
"failed_miscellaneous": []
}