{
"info": {
"nct_id": "NCT01262560",
"official_title": "Phase II Randomized Trial of Prophylactic Manuka Honey for the Reduction of Chemoradiation Therapy Induced Esophagitis-Related Pain During the Treatment of Lung Cancer",
"inclusion_criteria": "Healthy volunteers allowed\nMust have minimum age of 18 Years",
"exclusion_criteria": "",
"miscellaneous_criteria": "DISEASE CHARACTERISTICS:\n\n* Patients being treated with combination chemotherapy (definitive or adjuvant) and radiation therapy once daily for small cell or non-small cell lung cancer (primary population for the trial)\n\n * Patients can receive chemoradiotherapy while on a Radiation Therapy Oncology Group (RTOG) lung trial or while not being on a clinical trial\n * No patients receiving chemoradiotherapy while enrolled on a single institution trial or trials coordinated by other cooperative groups\n* No patients with metastatic disease\n* At least 5 cm of the esophagus must be in the 60 Gy isodose volume in 1.6 to 2.0 Gy fractions\n\nPATIENT CHARACTERISTICS:\n\n* Age 18 and up\n* Able to swallow thick liquids prior to treatment\n* Able to speak English or Spanish in order to complete required forms (verbal completion is adequate)\n* No patients with poorly controlled diabetes\n* No known hypersensitivity to honey\n\nPRIOR CONCURRENT THERAPY:\n\n* See Disease Characteristics\n* No patients who have received prior chemotherapy or radiation therapy\n* No patients receiving more than once daily treatments\n* Therapeutic use of honey other than the Manuka honey provided for this trial is not allowed while patients are on study\n* Patients must also avoid honey-flavored medical products and/or sugary, viscous substances\n* Amifostine is not permitted"
},
"inclusion_lines": [
{
"identified_line": {
"line": "Healthy volunteers allowed",
"criterions": [
{
"exact_snippets": "Healthy volunteers allowed",
"criterion": "volunteer health status",
"requirement": {
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"expected_value": "healthy"
}
}
]
},
"logical_structure": {
"and_criteria": [
{
"exact_snippets": "Healthy volunteers allowed",
"criterion": "volunteer health status",
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}
}
]
}
},
{
"identified_line": {
"line": "Must have minimum age of 18 Years",
"criterions": [
{
"exact_snippets": "minimum age of 18 Years",
"criterion": "age",
"requirement": {
"requirement_type": "N/A",
"expected_value": {
"operator": ">=",
"value": 18,
"unit": "Years"
}
}
}
]
},
"logical_structure": {
"and_criteria": [
{
"exact_snippets": "minimum age of 18 Years",
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"requirement_type": "N/A",
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"operator": ">=",
"value": 18,
"unit": "Years"
}
}
}
]
}
}
],
"exclusion_lines": [],
"miscellaneous_lines": [
{
"identified_line": {
"line": "* Patients being treated with combination chemotherapy (definitive or adjuvant) and radiation therapy once daily for small cell or non-small cell lung cancer (primary population for the trial)",
"criterions": [
{
"exact_snippets": "Patients being treated with combination chemotherapy",
"criterion": "combination chemotherapy treatment",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "radiation therapy once daily",
"criterion": "radiation therapy frequency",
"requirement": {
"requirement_type": "frequency",
"expected_value": "once daily"
}
},
{
"exact_snippets": "small cell or non-small cell lung cancer",
"criterion": "lung cancer type",
"requirement": {
"requirement_type": "type",
"expected_value": [
"small cell",
"non-small cell"
]
}
}
]
},
"logical_structure": {
"and_criteria": [
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"and_criteria": [
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"expected_value": true
}
},
{
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"requirement": {
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"expected_value": "once daily"
}
}
]
},
{
"exact_snippets": "small cell or non-small cell lung cancer",
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"requirement": {
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]
}
}
]
}
},
{
"identified_line": {
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"criterions": [
{
"exact_snippets": "Patients can receive chemoradiotherapy",
"criterion": "chemoradiotherapy",
"requirement": {
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"expected_value": true
}
},
{
"exact_snippets": "while on a Radiation Therapy Oncology Group (RTOG) lung trial",
"criterion": "RTOG lung trial participation",
"requirement": {
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"expected_value": true
}
},
{
"exact_snippets": "while not being on a clinical trial",
"criterion": "clinical trial participation",
"requirement": {
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"expected_value": false
}
}
]
},
"logical_structure": {
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"expected_value": true
}
},
{
"exact_snippets": "while on a Radiation Therapy Oncology Group (RTOG) lung trial",
"criterion": "RTOG lung trial participation",
"requirement": {
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"expected_value": true
}
}
]
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"criterion": "chemoradiotherapy",
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"expected_value": true
}
},
{
"exact_snippets": "while not being on a clinical trial",
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}
]
}
]
}
},
{
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"criterions": [
{
"exact_snippets": "No patients receiving chemoradiotherapy",
"criterion": "chemoradiotherapy",
"requirement": {
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"expected_value": false
}
},
{
"exact_snippets": "enrolled on a single institution trial",
"criterion": "enrollment in a single institution trial",
"requirement": {
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"expected_value": false
}
},
{
"exact_snippets": "trials coordinated by other cooperative groups",
"criterion": "enrollment in trials coordinated by other cooperative groups",
"requirement": {
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"expected_value": false
}
}
]
},
"logical_structure": {
"and_criteria": [
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"and_criteria": [
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"exact_snippets": "No patients receiving chemoradiotherapy",
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"requirement": {
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"expected_value": false
}
},
{
"exact_snippets": "enrolled on a single institution trial",
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}
}
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},
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}
}
]
}
},
{
"identified_line": {
"line": "* At least 5 cm of the esophagus must be in the 60 Gy isodose volume in 1.6 to 2.0 Gy fractions",
"criterions": [
{
"exact_snippets": "At least 5 cm of the esophagus must be in the 60 Gy isodose volume",
"criterion": "esophagus in 60 Gy isodose volume",
"requirement": {
"requirement_type": "length",
"expected_value": {
"operator": ">=",
"value": 5,
"unit": "cm"
}
}
},
{
"exact_snippets": "1.6 to 2.0 Gy fractions",
"criterion": "fraction size",
"requirement": {
"requirement_type": "range",
"expected_value": {
"comparisons": [
{
"operator": ">=",
"value": 1.6,
"unit": "Gy"
},
{
"operator": "<=",
"value": 2.0,
"unit": "Gy"
}
]
}
}
}
]
},
"logical_structure": {
"and_criteria": [
{
"exact_snippets": "At least 5 cm of the esophagus must be in the 60 Gy isodose volume",
"criterion": "esophagus in 60 Gy isodose volume",
"requirement": {
"requirement_type": "length",
"expected_value": {
"operator": ">=",
"value": 5,
"unit": "cm"
}
}
},
{
"exact_snippets": "1.6 to 2.0 Gy fractions",
"criterion": "fraction size",
"requirement": {
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"comparisons": [
{
"operator": ">=",
"value": 1.6,
"unit": "Gy"
},
{
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"value": 2.0,
"unit": "Gy"
}
]
}
}
}
]
}
},
{
"identified_line": {
"line": "* Age 18 and up",
"criterions": [
{
"exact_snippets": "Age 18 and up",
"criterion": "age",
"requirement": {
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"expected_value": {
"comparisons": [
{
"operator": ">=",
"value": 18,
"unit": "years"
}
]
}
}
}
]
},
"logical_structure": {
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"exact_snippets": "Age 18 and up",
"criterion": "age",
"requirement": {
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{
"operator": ">=",
"value": 18,
"unit": "years"
}
]
}
}
}
]
}
},
{
"identified_line": {
"line": "* Able to swallow thick liquids prior to treatment",
"criterions": [
{
"exact_snippets": "Able to swallow thick liquids",
"criterion": "ability to swallow thick liquids",
"requirement": {
"requirement_type": "ability",
"expected_value": true
}
}
]
},
"logical_structure": {
"and_criteria": [
{
"exact_snippets": "Able to swallow thick liquids",
"criterion": "ability to swallow thick liquids",
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"expected_value": true
}
}
]
}
},
{
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"criterions": [
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"requirement": {
"requirement_type": "languages",
"expected_value": [
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"Spanish"
]
}
},
{
"exact_snippets": "complete required forms (verbal completion is adequate)",
"criterion": "form completion ability",
"requirement": {
"requirement_type": "method",
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}
]
},
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}
}
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}
}
]
}
},
{
"identified_line": {
"line": "PRIOR CONCURRENT THERAPY:",
"criterions": [
{
"exact_snippets": "PRIOR CONCURRENT THERAPY",
"criterion": "prior concurrent therapy",
"requirement": {
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"expected_value": true
}
}
]
},
"logical_structure": {
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{
"exact_snippets": "PRIOR CONCURRENT THERAPY",
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}
}
]
}
},
{
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}
}
]
},
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}
}
]
}
},
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},
{
"exact_snippets": "No patients who have received prior ... radiation therapy",
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"expected_value": false
}
}
]
},
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"criterion": "prior chemotherapy",
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"expected_value": false
}
},
{
"exact_snippets": "No patients who have received prior ... radiation therapy",
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}
]
}
},
{
"identified_line": {
"line": "* Therapeutic use of honey other than the Manuka honey provided for this trial is not allowed while patients are on study",
"criterions": [
{
"exact_snippets": "Therapeutic use of honey other than the Manuka honey provided for this trial is not allowed",
"criterion": "therapeutic use of honey",
"requirement": {
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"expected_value": "Manuka honey provided for this trial"
}
}
]
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"logical_structure": {
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"exact_snippets": "Therapeutic use of honey other than the Manuka honey provided for this trial is not allowed",
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}
}
}
},
{
"identified_line": {
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"criterions": [
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"expected_value": true
}
},
{
"exact_snippets": "avoid ... sugary, viscous substances",
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"requirement": {
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}
]
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}
]
}
},
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"criterions": []
},
"logical_structure": {
"and_criteria": []
}
},
{
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"criterions": []
},
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}
}
],
"failed_inclusion": [],
"failed_exclusion": [],
"failed_miscellaneous": [
{
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{
"exact_snippets": "No patients with metastatic disease",
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}
}
]
},
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"expected_value": true
}
}
}
},
{
"identified_line": {
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"criterions": [
{
"exact_snippets": "No patients with poorly controlled diabetes",
"criterion": "diabetes",
"requirement": {
"requirement_type": "control",
"expected_value": "not poorly controlled"
}
}
]
},
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}
}
}
},
{
"identified_line": {
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"criterions": [
{
"exact_snippets": "No known hypersensitivity to honey",
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"requirement": {
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}
]
},
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}
}
},
{
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"expected_value": {
"operator": "<=",
"value": 1,
"unit": "times per day"
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}
}
]
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"unit": "times per day"
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}
}
}
},
{
"identified_line": {
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}
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}
]
}