Examples of using Active controlled in English and their translations into Romanian
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Active controlled studies.
Imprida HCT was studied in a double-blind, active controlled study in hypertensive patients.
A randomized, active controlled, long term study demonstrated that efficacy was maintained throughout a 1-year treatment period.
The safety and efficacy of dulaglutide was investigated in a placebo and active controlled(sitagliptin 100 mg daily) study of 104 weeks duration, all in combination with metformin.
In the active controlled studies, all patients were aged> 6years old(range 6-66 years) with an FEV1% predicted at screening of between 24% and 76%.
Dulaglutide was studied in a 52 week active controlled monotherapy study in comparison to metformin.
In this active controlled clinical trial, the most common reasons for discontinuation of therapy with Copalia HCT were dizziness and hypotension(0.7%).
The incidence of any adverse reactions potentially related to hypotension in a short-term active controlled study was 4.9% with Rasitrio versus up to 3.7% with dual combinations.
In the 2 active controlled a DVT/PE treatment trials, RE-COVER and RE-COVER II, a total of 2,553 patients were included in the safety analysis for dabigatran etexilate.
The safety and efficacy of dulaglutide was investigated in a placebo and active controlled(sitagliptin 100 mg daily) study of 104 weeks duration, all in combination with metformin.
An active controlled clinical trial(rosiglitazone up to 8 mg daily or metformin up to 2,000 mg daily) of 24 weeks duration was performed in 197 children(10-17 years of age) with type 2 diabetes.
Table 3: Results of a 104 week placebo and active controlled study with two doses of dulaglutide in comparison to sitagliptin.
Four multicenter studies with either Pravafenix 40 mg/160 mg or Pravastatin 40 mg or Simvastatin 20 mg were conducted: 3 studies included a 12 week randomized,double-blind, active controlled period with an open-label extension phase and one was a 24-week open-label study.
Table 5: Results of a 78 week active controlled study with two doses of dulaglutide in comparison to insulin glargine.
The safety and efficacy of Pixuvri as single-agent therapy were evaluated in a multicentre, randomised, active controlled trial in patients with relapsed or refractory aggressive NHL after receiving at least two prior therapies(PIX301).
Study E2100 was an open-label,randomised, active controlled, multicentre clinical trial evaluating Avastin in combination with paclitaxel for locally recurrent or metastatic breast cancer in patients who had not previously received chemotherapy for locally recurrent and metastatic disease.
The effect of age on the immune response to IXIARO and JE-VAX was assessed as a secondary endpoint in this active controlled study, comparing subjects aged≥ 50 years of age(N=262, mean age 59.8) with those below 50 years of age(N=605, mean age 33.9).
Table 2: Results of a 52 week active controlled monotherapy study with two doses of dulaglutide in comparison to metformin.
Table 4: Efficacy results at 104 week in an active controlled study comparing empagliflozin to glimepiride as add on to metformina.
Adverse reactions observed during the 1-year(long term) active controlled(muscarinic antagonist) study were similar in type and severity to those observed in the three 12-week phase 3 double blind, placebo controlled studies.
Immunogenicity was evaluated in randomised,multicenter, active controlled clinical trials that enrolled children(2-10 years of age), adolescents(11-18 years of age), adults(19-55 years of age) and older adults(56-65 years of age).
Trial E2100 was an open-label,randomised, active controlled, multicentre clinical trial evaluating Avastin in combination with paclitaxel for locally recurrent or metastatic breast cancer in patients who had not previously received chemotherapy for locally recurrent and metastatic disease.
Study GS-US-174-0108 is a randomised,double-blind, active controlled study evaluating the safety and efficacy of tenofovir disoproxil fumarate(n= 45), emtricitabine plus tenofovir disoproxil fumarate(n= 45), and entecavir(n= 22), in patients with decompensated liver disease.
Immunogenicity of the vaccine was evaluated in a randomized, active controlled, observer blinded, multicenter Phase 3 clinical trial including 867 healthy male and female subjects given IXIARO or the US licensed JEV vaccine JE VAX(on a 0, 7 and 28 day schedule by subcutaneous injection).
Active control track.
Active Control optimizes picture quality whatever the source.
Fixed crash during search after active control on find panel has been hidden.
The ACR8 Active Control Retractor.
Active Control+ Light sensor.
Active Control(a).