{
"info": {
"nct_id": "NCT00062231",
"official_title": "Oral Empirical Therapy of Fever in Low-Risk Neutropenic Cancer Patients: A Prospective, Double-Blind, Randomized, Multicenter Trial Comparing Monotherapy (Single Daily Dose Moxifloxacin) With Combination Therapy (Ciprofloxacin Plus Amoxicillin/Clavulanic Acid)",
"inclusion_criteria": "Healthy volunteers allowed\nMust have minimum age of 18 Years",
"exclusion_criteria": "",
"miscellaneous_criteria": "DISEASE CHARACTERISTICS:\n\n* Diagnosis of cancer with developing febrile neutropenia\n\n * Neutropenia defined as an absolute granulocyte count of less than 1,000/mm^3, expected to fall to less than 500/mm^3 within 24 hours, secondary to administration of chemotherapy and/or radiotherapy within the past 30 days\n * Fever defined as an oral temperature greater than 38.5ºC once, or 38°C or greater on 2 or more occasions at least 1 hour apart during a 12-hour period, and suspected to be due to infection\n* Expected low risk of serious medical complications as predicted by a Multinational Association for Supportive Care in Cancer risk-index score of greater than 20\n* No obvious signs of exit-site or tunnel intravascular catheter infection\n* No known or suspected CNS infection\n* No known or highly suspected bacterial, viral, or fungal infection\n\nPATIENT CHARACTERISTICS:\n\nAge\n\n* 18 and over\n\nPerformance status\n\n* Not specified\n\nLife expectancy\n\n* No high probability of death within 48 hours before study enrollment (i.e., patients who are moribund or comatose for any reason with little hope of recovery OR patients in danger of, or in hepatic stupor or coma)\n\nHematopoietic\n\n* See Disease Characteristics\n* No signs or symptoms of uncontrolled bleeding\n\nHepatic\n\n* Bilirubin no greater than 3 times upper limit of normal (ULN)\n* Alkaline phosphatase no greater than 3 times ULN\n* AST and ALT no greater than 5 times ULN\n* No severe hepatic dysfunction\n\nRenal\n\n* Creatinine no greater than 3.4 mg/dL\n* Creatinine clearance at least 25 mL/min\n* No renal failure requiring hemodialysis or peritoneal dialysis\n\nCardiovascular\n\n* No prior symptomatic arrhythmias\n* No clinically relevant bradycardia\n* No QTc interval prolongation\n* No uncorrected hypokalemia\n* No signs or symptoms of hypotension (systolic less than 90 mm Hg)\n\nPulmonary\n\n* No signs or symptoms of respiratory insufficiency\n\nOther\n\n* Not pregnant or nursing\n* Fertile patients must use effective contraception\n* Able to swallow oral medication\n* No contraindication for oral drug intake\n* No condition likely to severely impair drug absorption\n* No prior immediate or accelerated reaction to penicillin, cephalosporin, or fluoroquinolone antibiotics\n* No known allergy or hypersensitivity to any antibiotics in this study or other quinolones\n* No signs or symptoms of severe dehydration\n* No signs or symptoms of shock\n* No other signs or symptoms at presentation that would necessitate IV supportive therapy\n\nPRIOR CONCURRENT THERAPY:\n\nBiologic therapy\n\n* Not specified\n\nChemotherapy\n\n* See Disease Characteristics\n\nEndocrine therapy\n\n* Not specified\n\nRadiotherapy\n\n* See Disease Characteristics\n\nSurgery\n\n* Not specified\n\nOther\n\n* More than 4 days since prior antibacterial agents except for the following:\n\n * A single (oral or parenteral therapeutic) dose after initial diagnosic work-up and within the last 8 hours\n * Low-dose cotrimoxazole (i.e., no more than 480 mg daily or 960 mg 3 times per week) prophylaxis of Pneumocystis carinii pneumonia\n* More than 30 days since prior investigational drugs\n* No prior randomization in this study\n* No other concurrent antimicrobial agents\n* No class IA or class III antiarrhythmic drugs or other concurrent drugs that prolong the QTc interval"
},
"inclusion_lines": [
{
"identified_line": {
"line": "Healthy volunteers allowed",
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}
}
]
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},
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}
}
]
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],
"exclusion_lines": [],
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}
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}
}
]
},
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}
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}
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{
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"operator": "<",
"value": 1000,
"unit": "mm^3"
}
}
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"unit": "mm^3"
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},
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}
},
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}
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}
},
{
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}
}
]
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]
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}
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]
}
},
{
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}
]
},
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}
]
}
},
{
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"criterion": "class IA or class III antiarrhythmic drugs",
"requirement": {
"requirement_type": "presence",
"expected_value": false
}
},
{
"exact_snippets": "other concurrent drugs that prolong the QTc interval",
"criterion": "drugs that prolong the QTc interval",
"requirement": {
"requirement_type": "presence",
"expected_value": false
}
}
]
}
},
{
"identified_line": {
"line": "DISEASE CHARACTERISTICS:",
"criterions": []
},
"logical_structure": {
"and_criteria": []
}
},
{
"identified_line": {
"line": "PATIENT CHARACTERISTICS:",
"criterions": []
},
"logical_structure": {
"and_criteria": []
}
},
{
"identified_line": {
"line": "* Not specified",
"criterions": []
},
"logical_structure": {
"and_criteria": []
}
},
{
"identified_line": {
"line": "Other",
"criterions": []
},
"logical_structure": {
"and_criteria": []
}
},
{
"identified_line": {
"line": "* Not pregnant or nursing",
"criterions": [
{
"exact_snippets": "Not pregnant",
"criterion": "pregnancy",
"requirement": {
"requirement_type": "status",
"expected_value": false
}
},
{
"exact_snippets": "not ... nursing",
"criterion": "nursing",
"requirement": {
"requirement_type": "status",
"expected_value": false
}
}
]
},
"logical_structure": {
"and_criteria": [
{
"exact_snippets": "Not pregnant",
"criterion": "pregnancy",
"requirement": {
"requirement_type": "status",
"expected_value": false
}
},
{
"exact_snippets": "not ... nursing",
"criterion": "nursing",
"requirement": {
"requirement_type": "status",
"expected_value": false
}
}
]
}
},
{
"identified_line": {
"line": "* Not specified",
"criterions": []
},
"logical_structure": {
"and_criteria": []
}
},
{
"identified_line": {
"line": "* Not specified",
"criterions": []
},
"logical_structure": {
"and_criteria": []
}
},
{
"identified_line": {
"line": "* Not specified",
"criterions": []
},
"logical_structure": {
"and_criteria": []
}
},
{
"identified_line": {
"line": "Other",
"criterions": []
},
"logical_structure": {
"and_criteria": []
}
}
],
"failed_inclusion": [],
"failed_exclusion": [],
"failed_miscellaneous": [
{
"identified_line": {
"line": "* No known or suspected CNS infection",
"criterions": [
{
"exact_snippets": "No known or suspected CNS infection",
"criterion": "CNS infection",
"requirement": {
"requirement_type": "presence",
"expected_value": false
}
}
]
},
"logical_structure": {
"not_criteria": {
"exact_snippets": "No known or suspected CNS infection",
"criterion": "CNS infection",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
}
}
},
{
"identified_line": {
"line": "* No signs or symptoms of uncontrolled bleeding",
"criterions": [
{
"exact_snippets": "No signs or symptoms of uncontrolled bleeding",
"criterion": "uncontrolled bleeding",
"requirement": {
"requirement_type": "presence",
"expected_value": false
}
}
]
},
"logical_structure": {
"not_criteria": {
"exact_snippets": "No signs or symptoms of uncontrolled bleeding",
"criterion": "uncontrolled bleeding",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
}
}
},
{
"identified_line": {
"line": "* No clinically relevant bradycardia",
"criterions": [
{
"exact_snippets": "No clinically relevant bradycardia",
"criterion": "bradycardia",
"requirement": {
"requirement_type": "severity",
"expected_value": "not clinically relevant"
}
}
]
},
"logical_structure": {
"not_criteria": {
"exact_snippets": "No clinically relevant bradycardia",
"criterion": "bradycardia",
"requirement": {
"requirement_type": "severity",
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}
}
}
},
{
"identified_line": {
"line": "* No QTc interval prolongation",
"criterions": [
{
"exact_snippets": "No QTc interval prolongation",
"criterion": "QTc interval",
"requirement": {
"requirement_type": "prolongation",
"expected_value": false
}
}
]
},
"logical_structure": {
"not_criteria": {
"exact_snippets": "No QTc interval prolongation",
"criterion": "QTc interval",
"requirement": {
"requirement_type": "prolongation",
"expected_value": true
}
}
}
},
{
"identified_line": {
"line": "* No contraindication for oral drug intake",
"criterions": [
{
"exact_snippets": "No contraindication for oral drug intake",
"criterion": "contraindication for oral drug intake",
"requirement": {
"requirement_type": "presence",
"expected_value": false
}
}
]
},
"logical_structure": {
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"exact_snippets": "No contraindication for oral drug intake",
"criterion": "contraindication for oral drug intake",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
}
}
},
{
"identified_line": {
"line": "* No prior randomization in this study",
"criterions": [
{
"exact_snippets": "No prior randomization in this study",
"criterion": "prior randomization",
"requirement": {
"requirement_type": "presence",
"expected_value": false
}
}
]
},
"logical_structure": {
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"exact_snippets": "No prior randomization in this study",
"criterion": "prior randomization",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
}
}
}
]
}