Examples of using Randomized study in English and their translations into Bulgarian
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A double blind randomized study was carried out in 32 patients with alcoholic disease.
American scientist's drinking water to lose weight from the Virginia Polytechnic Institute in a randomized study found out how water helps to lose weight.
Efficacy results from randomized study in patients with pancreatic adenocarcinoma(Intent-to-treat population).
The safety and efficacy of docetaxel in the induction treatment of patients with squamous cell carcinoma of the head and neck(SCCHN) was evaluated in a phase III, multicenter,open-label, randomized study(TAX323).
The CHMP noted the submitted double blind,comparative, randomized study and considered it to be adequately designed.
In a randomized study involving men and women in their mid-60s, walking three times a week for a year….
That further research- a double-blind,placebo-controlled, randomized study- was recently published in the journal Parkinsonism& Related Disorders.6.
The randomized study involved 250 people considered at risk for developing colorectal cancer because of either risk factors or having a precancerous polyp removed.
Induction chemotherapy followed by radiotherapy(TAX323) The safety and efficacy of docetaxel in the induction treatment of patients with squamous cell carcinoma of the head and neck(SCCHN) was evaluated in a phase III, multicenter,open-label, randomized study(TAX323).
Of the 229 patients in the randomized study who received Abraxane monotherapy for breast cancer, 13% were at least 65 years of age and< 2% were 75 years and older.
When they launched the trial in 2015, the number of Ebola cases in Guinea had already declined, andthere were too few cases to run a meaningful traditional randomized study(giving the vaccine to a randomly selected group and comparing it with a control group that doesn't get the vaccine).
This comparison may be done in a randomized study of two treatment arms or by evaluating a single new treatment and comparing the results with those previously obtained with standard therapy.
The pharmacokinetics, safety and efficacy of Jivi for on demand treatment, prophylaxis with three regimens(two times per week 30-40 IU/kg, every 5-days 45-60 IU/kg and every 7-days 60 IU/kg) and haemostasis during major surgeries were evaluated in a multinational, open-label, uncontrolled,partially randomized study which was performed in compliance with the agreed Paediatric Investigation Plan.
The OMEGA trial was a large prospective,double blind, randomized study including a population highly representative of the target population including the use of standard of care treatment.
Randomized study with over 3000 human subjects for seven clinical years showed that cancer risk was cut by 60% for those with the highest intake of allium containing vegetables, including aged garlic.
Of the 421 patients with pancreatic adenocarcinoma in the randomized study who received Abraxane in combination with gemcitabine, 41% were 65 years and older and 10% were 75 years and older.
The randomized study was partially double-blinded so medical staff did not know what treatment each participating family received, when distributing their sealed syringe containing envelopes.
Patients with operable node-positive breast cancer(TAX 316) Data from a multicenter open label randomized study support the use of docetaxel for the adjuvant treatment of patients with operable node-positive breast cancer and KPS≥80%, between 18 and 70 years of age.
Phase III randomized study of concurrent tretinoin and chemotherapy with or without arsenic trioxide(As2O3) as initial consolidation therapy followed by maintenance with intermittent tretinoin therapy versus intermittent tretinoin plus mercaptopurine and methotrexate for patients with untreated acute promyelocytic leukemia.
Of the 514 patients with non-small cell lung cancer in the randomized study who received Abraxane in combination with carboplatin, 31% were 65 years or older and 3.5% were 75 years or older.
In a double-blind randomized study in 90 children aged 1 to 6 years, which was followed by a oneyear open-label extension, two deaths and isolated cases of marked liver transaminases elevations were observed.
Of the 421 patients with pancreatic adenocarcinoma in the randomized study who received human serum albumin-paclitaxel nanoparticles in combination with gemcitabine, 41% were 65 years and older and 10% were 75 years and older.
Of the 229 patients in the randomized study who received human serum albumin-paclitaxel nanoparticles monotherapy for breast cancer, 13% were at least 65 years of age and< 2% were 75 years and older.
Of the 514 patients with non-small cell lung cancer in the randomized study who received human serum albumin-paclitaxel nanoparticles in combination with carboplatin, 31% were 65 years or older and 3.5% were 75 years or older.
Linagliptin cardiovascular safety study(CAROLINA) CAROLINA was a randomized study in 6033 patients with early type 2 diabetes and increased CV risk or established complications who were treated with linagliptin 5 mg(3023) or glimepiride 1-4mg(3010) added to standard of care(including background therapy with metformin in 83% of patients) targeting regional standards for HbA1c and CV risk factors.
This comparison may be done in a randomized study of two treatment arms or by evaluating a single new treatment and comparing the results with those previously obtained with standard therapy.
Data from a multicenter open label randomized study support the use of docetaxel for the adjuvant treatment of patients with operable node-positive breast cancer and KPS≥ 80%, between 18 and 70 years of age.
Linagliptin cardiovascular and renal safety study(CARMELINA) CARMELINA was a randomized study in 6979 patients with type 2 diabetes with increased CV risk evidenced by a history of established macrovascular or renal disease who were treated with linagliptin 5 mg(3494) or placebo(3485) added to standard of care targeting regional standards for HbA1c, CV risk factors and renal disease.
A pivotal phase 3 randomized, crossover PK andPD study(which was also the first ever randomized study with immediate-release cysteamine bitartrate) demonstrated that at steady-state, patients receiving PROCYSBI every 12 hours(Q12H) maintained a comparable depletion of WBC cystine levels compared to immediate-release cysteamine bitartrate every 6 hours(Q6H).
Summary of key results from four phase III randomized studies evaluating the benefit of MabThera with different chemotherapy regimens in follicular lymphoma.