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10.1007/s11606-021-06888-1

Multi-site, 2-arm (1:1), non-blinded randomized clinical trial.

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10.1002/mpr.1887

METHODS A non-blinded randomized controlled trial was conducted.

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10.1007/s00192-021-04904-w

This was a non-blinded randomized trial comparing methenamine hippurate with trimethoprim for the prevention of recurrent urinary tract infections 12 months after starting treatment [1].

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10.1016/j.ajog.2020.12.113

STUDY DESIGN: A pragmatic non-blinded randomized controlled non-inferiority trial performed at two medical sites.

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10.1016/j.cmpb.2020.105892

METHODS A non-blinded randomized controlled trial was conducted.

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10.21203/RS.3.RS-404662/V1

Design:A non-blinded randomized controlled trial.

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10.7759/cureus.15510

Materials and methods This is a prospective, non-blinded randomized controlled trial conducted in newly diagnosed PCOS women aged 18 to 45 years.

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10.21203/RS.3.RS-455096/V1

Methods: The feasibility study follows a two-part design owing to Covid-19 related adaptations to project design: a) A non-blinded randomized controlled trial (RCT) of 12 weeks of bicycle-based HIIT, delivered twice weekly in a face-to-face, one-to-one setting, compared to treatment as usual (TAU).

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10.3389/fvets.2021.664112

Design: A prospective, non-blinded randomized study design was used.

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10.1007/s00192-021-04849-0

We present a non-blinded randomized trial comparing methenamine hippurate with trimethoprim for the prevention of recurrent UTI at 12 months after starting treatment.

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10.21203/rs.3.rs-534437/v1

Design: Multicentre, superiority, non-blinded randomized controlled trial.

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10.1007/s00464-020-08277-x

This prospective non-blinded randomized controlled trial allocated 51 patients, who were candidates for a LRYGB, into DEP+SVC (intervention, n = 26) or SVC (control, n = 25) groups.

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10.1016/J.RASD.2021.101804

Method We conducted a non-blinded randomized trial to compare the effect of the PTR to a business as usual, less intensive intervention (i.

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10.1158/1538-7445.SABCS20-PS12-06

This non-blinded randomized phase II trial of neoadjuvant fulvestrant with or without enzalutamide was performed in women with T2 or greater ER+/Her2- primary breast cancer.

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Non Blinded Randomized

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Aug 11, 2022

What is/are Non Blinded Randomized?

Non Blinded Randomized - Multi-site, 2-arm (1:1), non-blinded randomized clinical trial. ^[1] METHODS A non-blinded randomized controlled trial was conducted. ^[2] This was a non-blinded randomized trial comparing methenamine hippurate with trimethoprim for the prevention of recurrent urinary tract infections 12 months after starting treatment [1]. ^[3] STUDY DESIGN: A pragmatic non-blinded randomized controlled non-inferiority trial performed at two medical sites. ^[4] METHODS A non-blinded randomized controlled trial was conducted. ^[5] Design:A non-blinded randomized controlled trial. ^[6] Materials and methods This is a prospective, non-blinded randomized controlled trial conducted in newly diagnosed PCOS women aged 18 to 45 years. ^[7] Methods: The feasibility study follows a two-part design owing to Covid-19 related adaptations to project design: a) A non-blinded randomized controlled trial (RCT) of 12 weeks of bicycle-based HIIT, delivered twice weekly in a face-to-face, one-to-one setting, compared to treatment as usual (TAU). ^[8] Design: A prospective, non-blinded randomized study design was used. ^[9] We present a non-blinded randomized trial comparing methenamine hippurate with trimethoprim for the prevention of recurrent UTI at 12 months after starting treatment. ^[10] Design: Multicentre, superiority, non-blinded randomized controlled trial. ^[11] This prospective non-blinded randomized controlled trial allocated 51 patients, who were candidates for a LRYGB, into DEP+SVC (intervention, n = 26) or SVC (control, n = 25) groups. ^[12] Method We conducted a non-blinded randomized trial to compare the effect of the PTR to a business as usual, less intensive intervention (i. ^[13] This non-blinded randomized phase II trial of neoadjuvant fulvestrant with or without enzalutamide was performed in women with T2 or greater ER+/Her2- primary breast cancer. ^[14]