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Smart Reasoning:

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Qaagi - Book of Why

Causes

Effects

The researchersdesigneda randomized , double arm , open label , active - controlled clinical trial

a factorcausingformation of a randomized , double - blind , active - control trial

The Labdesigneda randomized controlled trial for the rollout of body - worn cameras

so with the help of several colleaguesdesigneda study based on a randomized controlled trial

the help of several colleaguesdesigneda study based on a randomized controlled trial

the studywas ... designedto be a randomized controlled trial ( read more about randomized control trials

We attemptedto designa robust , quasi - experimental study : a non - randomised controlled trial

interventionsdesignedto promote physical activity by means of the Internet as evaluated by randomized controlled trials

by the disease(passive) caused byautonomic dysfunction ... : Results from a randomized controlled trial

Foodcausesinhibitory motor effects of randomized - controlled trial

to a team of Extension Specialists and researchers from Texas A&M University and the TAMU and University of Texas Schools of Public Health(passive) was designedA randomized , controlled trial study

a team of Extension Specialists and researchers from Texas A&M University and the TAMU and University of Texas Schools of Public Health(passive) was designed byA randomized , controlled trial study

Roy K. Greenberg , M.D.(passive) led byInd.--(HSMN NewsFeed)--A non - randomized , controlled study

Jon S. Matsumura , M.D.(passive) led byInd.--(HSMN NewsFeed)--A non - randomized , controlled study

by Jon S. Matsumura , M.D.(passive) led byInd.--(HSMN NewsFeed)--A non - randomized , controlled study

by Wennberg(passive) led bya randomized controlled trial study

Cambridge researcher Barak Ariel(passive) led byOne multi - site , transnational randomized controlled trial

various inclusion and exclusion criteriaare setin randomized controlled trials - designed comparative studies

to compare the clinical outcome of early surgical strategy versus a conservative approach(passive) is designedA randomized controlled trial

to evaluate the clinical and quality of life(passive) was designedA randomized controlled trial

The authors of this studydesigneda randomized controlled trial

to evaluate the efficacy of the medication in lowering cholesterol(passive) is designedA randomized controlled trial

Researchershave designeda randomized controlled trial

Dr. Hutchinson(passive) led byA randomized controlled trial

with participants being randomly placed under the treatment(passive) will be designedA randomized controlled trial

The investigatorshave designeda randomized controlled trial

to test a stage - based smoking cessation intervention on Facebook tailored for smokers aged 18 to 25(passive) has been designedA randomized controlled trial

The present protocoldesigneda randomized controlled trial

The research teamdesigneda randomized controlled trial

to assess the effectiveness of the EBP training program(passive) was designedA randomized controlled trial

The non - blinding design is knownto causeoverestimation in randomized controlled trials

to compare the MIPS technique to the linear incision technique with soft tissue preservation(passive) is designedA multicenter randomized controlled trial

to evaluate the effect of chiropractic treatment on crying time and other symptoms associated with infantile colic(passive) was designedA randomized controlled trial

Dr. Margaret Kemeny(passive) led byA randomized controlled trial

The choice of an adequate control group is criticalwhen designinga randomized controlled trial

Laura Steenbergen and her colleagues(passive) led byA randomized controlled trial

To prove that e - cigarettes can help you quit smoking , you haveto designa randomized controlled trial

Dr. Morrison - Beedy and recently published in the Journal of Adolescent Health(passive) led byA randomized controlled trial

doctoral student Shelley L. Patel that is currently underway(passive) led bya randomized controlled trial

Bente Stallknecht , Professor , Department of Biomedical Sciences , University of Copenhagen(passive) led bya randomized controlled trial

to evaluate the safety and tolerability of CD101 in women with moderate to severe episodes of VVCdesignedto evaluate the safety and tolerability of CD101 in women with moderate to severe episodes of VVC

to evaluate the efficacy and safety of the PDS in people with wet age - related macular degeneration ( AMDdesignedto evaluate the efficacy and safety of the PDS in people with wet age - related macular degeneration ( AMD

to compare thedesignedto compare the

to compare these regimenswas designedto compare these regimens

The study(passive) was designedThe study

to compare the safety ( including tolerability and immunogenicity ) , pharmacokinetics , and pharmacodynamics of three doses of weekly TransCon GH to daily growth hormone ( Omnitropedesignedto compare the safety ( including tolerability and immunogenicity ) , pharmacokinetics , and pharmacodynamics of three doses of weekly TransCon GH to daily growth hormone ( Omnitrope

Clinical Trial(passive) was designedClinical Trial

in the U. Patientscausedin the U. Patients

Rural settingsettingRural setting

to enroll approximately 100 patients with hemophilia A or B without inhibitors receiving prior on - demand therapydesignedto enroll approximately 100 patients with hemophilia A or B without inhibitors receiving prior on - demand therapy

of patients with stable coronary artery disease or acute coronarycomposedof patients with stable coronary artery disease or acute coronary

to enroll approximately 50 patients with hemophilia A or B with inhibitors receiving prior on - demand therapydesignedto enroll approximately 50 patients with hemophilia A or B with inhibitors receiving prior on - demand therapy

to evaluate the efficacy , safety and tolerability of oral androgen therapy in patients having testosterone deficiency and a randomized placebo - controlled clinical studydesignedto evaluate the efficacy , safety and tolerability of oral androgen therapy in patients having testosterone deficiency and a randomized placebo - controlled clinical study

to train attention for children , adolescents , and adultsdesignedto train attention for children , adolescents , and adults

to compare the safety ( including tolerability and immunogenicity ) , pharmacokinetics , and pharmacodynamics of three doses of weekly TransCon GH to daily growth hormone ( Omnitropedesignedto compare the safety ( including tolerability and immunogenicity ) , pharmacokinetics , and pharmacodynamics of three doses of weekly TransCon GH to daily growth hormone ( Omnitrope

to test this hypothesisdesignedto test this hypothesis

to compare treatment efficacy , functional outcomes , cost - effectiveness , and quality of life for 2100 patients suffering from CLIdesignedto compare treatment efficacy , functional outcomes , cost - effectiveness , and quality of life for 2100 patients suffering from CLI

to test this hypothesisdesignedto test this hypothesis

to study the impact of multiple micronutrient salt ( micronutrient group ) in comparison with nutrition education ( education group ) and no intervention ( control group ) on haemoglobin , serum ferritin , soluble transferrin receptor , body iron stores , serum retinol and urinary iodine outcomes over a period of 8 monthsdesignedto study the impact of multiple micronutrient salt ( micronutrient group ) in comparison with nutrition education ( education group ) and no intervention ( control group ) on haemoglobin , serum ferritin , soluble transferrin receptor , body iron stores , serum retinol and urinary iodine outcomes over a period of 8 months

to enroll approximately 50 patients with hemophilia A or B with inhibitors receiving prior on - demand therapydesignedto enroll approximately 50 patients with hemophilia A or B with inhibitors receiving prior on - demand therapy

in better outcomes than individualized drug therapy alonewould resultin better outcomes than individualized drug therapy alone

to investigate whether remote ischemic pre-designedto investigate whether remote ischemic pre-

to investigate whether remote ischemic pre- and/or post - conditioning of the arm reduce the incidence of AF following CABG surgerydesignedto investigate whether remote ischemic pre- and/or post - conditioning of the arm reduce the incidence of AF following CABG surgery

that drinking green smoothies may even contribute to improved blood pressure and general wellnesshas discoveredthat drinking green smoothies may even contribute to improved blood pressure and general wellness

to examine the feasibility and acceptability of mHealth tools ( electronic pill boxes and smartphones ) and communication feedback on medication adherence among people living with HIV ( PLH ) with cocaine use disordersdesignedto examine the feasibility and acceptability of mHealth tools ( electronic pill boxes and smartphones ) and communication feedback on medication adherence among people living with HIV ( PLH ) with cocaine use disorders

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Smart Reasoning:

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