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Property:Exclusion criteria

From CAMIH

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Showing 20 pages using this property.
M
N
Oral candidiasis or other oral lesions (e.g., stomatitis, necrosis, and ulcers), cranial nerve injuries, and metabolic/endocrine disorders that may have effects on taste perception  +
Scleroderma, large breast with an inter-field of more than 25cm, or prior radiotherapy to the same breast, indication to lymph node irradiation  +
Receiving prior treatment for advanced or metastatic disease; taking 2000 IU/d or greater of vitamin D<sub>3</sub>, had symptomatic genitourinary stones within the past year, or were taking thiazide diuretics.  +
Drank tea regularly within 1 month of enrollment (more than 6 servings of hot tea or 12 servings of iced tea or equivalent combination per week); receiving other investigational agents; history of allergic reactions attributed to compounds of similar chemical to polyphenon E; uncontrolled intercurrent illness  +
Aromatase inhibitor therapy in the last 6 weeks, history of kidney stones, hypercalcemia at baseline, history of symptomatic hypercalcemia or hyperparathyroidism, baseline 25-OH Vitamin D level >50 ng/mL, currently taking phenytoin or phenobarbital, currently taking cholestyramine or orlistat, malabsorption syndrome, or chronic granulomata forming disorders, such as sarcoidosis or tuberculosis  +
O
* Previous liver surgery. * Body weight loss >10% during the 6 months before surgery. * Presence of distant metastases. * Seriously impaired function of vital organs due to respiratory, renal, or heart disease. * Biliary cancer, due to the need for biliary resection, bilioenteric anastomosis, and lymphadenectomy during hepatectomy for this condition.   +
Pregnant or lactating, or planning to become pregnant; history of hypersensitivity or severe adverse reaction to fluoropyrimidines; serious concurrent disease (including interstitial pneumonia, pulmonary fibrosis, intestinal paralysis, ileus, poorly controlled diabetes, liver cirrhosis or hepatitis (type B or C), poorly controlled hypertension, history of myocardial infarction or unstable angina within past 6 months); active multiple primary cancer (disease-free less than 5 years); concurrent infectious disease; judged to be unsuitable for participation in the clinical study by the investigator for any other reason  +
P
Previous chemotherapeutic treatment or regimens including other neurotoxic drugs associated with cisplatin  +
Previous chemotherapeutic treatment or regimens including other neurotoxic drugs associated with cisplatin  +
Participation in another study with different drugs; history of bone marrow or stem cell transplantation; presence of respiratory, cardiovascular, liver, renal, metabolic, or gastrointestinal diseases; and history of motion sickness  +
White blood cells outside normal reference window; Hb < 11 g/dL; prior endocrine treatment; <5 year life-expectancy; ECOG score >1; incontinence/urinary retention; critical comorbidity (e.g. cardiovascular disease, chronic obstructive pulmonary disease, insulin dependent diabetes mellitus, vasculitis, inflammatory bowel syndrome or other conditions with potential influence on radiation therapy)  +
Patients receiving long-term methadone therapy for pain; major psychiatric or cardiovascular disorder; epilepsy; significant renal or hepatic impairment; pregnant, lactating or not using adequate contraception; patients, who had received or who were due to receive therapies expected to change the pain (such as radiotherapy, or chemotherapy or hormonal therapy); marijuana use, cannabinoid-based medications or rimonabant within 30 days of study entry, and unwilling to abstain for the duration of the study  +
R
With baseline serum corrected total calcium >10.5 mg/dl, phosphorous >4.5 mg/dl, magnesium >2.5 mg/dl, nephrolithiasis in the past 5 years, calcitriol therapy in the previous 30 days, hypersensitivity or inability to take oral calcitriol  +