Common use of Outline of Study Clause in Contracts

Outline of Study. This will be a prospective, multi-site, randomized, parallel-group, open-label study comparing 2 daily disposable contact lenses. The expected duration of subject participation in the study is approximately 4 weeks, with 3 scheduled visits. The study is expected to be completed in approximately 8 weeks. 4 TREATMENTS ADMINISTERED Subjects will be randomized in a 1:1 manner to receive treatment with DAILIES TOTAL1 or Acuvue Oasys 1-Day.

Appears in 1 contract

Samples: classic.clinicaltrials.gov

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Outline of Study. This will be a prospective, multi-site, prospective, randomized, parallelsubject-group, open-label masked study comparing 2 daily disposable contact lenses. The expected duration of subject participation in the study is approximately 4 weeksup to 64 days, with 3 5 scheduled visits. The study is expected to be completed in approximately 8 weeks3 months. 4 TREATMENTS ADMINISTERED Subjects will be randomized in a 1:1 manner to receive treatment with DAILIES TOTAL1 in crossover sequence: Test product then Control product or Acuvue Oasys 1-DayControl product then Test product, respectively.

Appears in 1 contract

Samples: Investigator Agreement

Outline of Study. This will be a prospective, multi-site, prospective, randomized, parallelparallel crossover, double-group, open-label masked study comparing 2 daily disposable 4 contact lenses. The expected duration of subject participation in the study is approximately 4 weeks20 days, with 3 scheduled visits. The study is expected to be completed in approximately 8 7 weeks. 4 TREATMENTS ADMINISTERED Subjects will be randomized in a 1:1 manner to receive treatment with DAILIES TOTAL1 or Acuvue Oasys 1-Day.

Appears in 1 contract

Samples: classic.clinicaltrials.gov

Outline of Study. This will be a prospective, multi-site, randomizedprospective, parallel-groupsingle arm, open-label study comparing 2 daily disposable examining 1 type of contact lenseslens. The expected duration of subject participation in the study is approximately 4 weeks7 days, with up to 3 scheduled visits. The study is expected to be completed in approximately 8 6 weeks. 4 TREATMENTS ADMINISTERED Subjects All subjects will be randomized in a 1:1 manner receive the test lens to receive treatment with DAILIES TOTAL1 or Acuvue Oasys 1-Daywear bilaterally throughout the study duration.

Appears in 1 contract

Samples: Investigator Agreement

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Outline of Study. This will be a prospective, multi-site, randomized, parallelcrossover, double-group, open-label masked study comparing 2 daily disposable contact lenses. The expected duration of subject participation in the study is approximately 4 weeks20 days, with 3 scheduled visits. The study is expected to be completed in approximately 8 5 weeks. 4 TREATMENTS ADMINISTERED Subjects will be randomized in a 1:1 manner to receive treatment with DAILIES TOTAL1 or Acuvue Oasys 1-Day.

Appears in 1 contract

Samples: clinicaltrials.gov

Outline of Study. This will be a prospective, multi-site, randomizedprospective, parallel-groupsingle arm, open-label study comparing 2 daily disposable examining 1 type of contact lenseslens. The expected duration of subject participation in the study is approximately 4 2 weeks, with up to 3 scheduled visits. The study is expected to be completed in approximately 8 5 weeks. 4 TREATMENTS ADMINISTERED Subjects All subjects will be randomized in a 1:1 manner receive the test lens to receive treatment with DAILIES TOTAL1 or Acuvue Oasys 1-Daywear bilaterally throughout the study duration.

Appears in 1 contract

Samples: Investigator Agreement

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