Introduction to Subjects Randomized

Subjects randomized to nutraceutical treatment experienced a significant improvement in triglycerides (TG= -32.

Patients were randomized in two groups: group 1 took Frinozol nasal spray 2 sprays per each nostril three times a day for 7 days, subjects randomized to the group 2 took Vibrocil at the same dose and treatment regimen.

Of 72 subjects randomized, 59 completed treatment.

Subjects randomized for delayed provision did not use an AFO in the first eight weeks of the study.

MethodsA two center trial of 104 hemodialysis subjects randomized to lower range LRG 0.

Having subjects randomized to a placebo group helps determine whether side effects are due to a drug or not.

This was not seen in subjects randomized to TCT (r=-0.

One large randomized trial (CHAMPION) proved that a direct pulmonary pressure monitor system (CardioMEMS) substantially reduced heart failure hospitalizations in subjects randomized to active pulmonary pressure-guided management.

Patients were randomized in two groups: group 1 took Frinozol nasal spray 2 sprays per each nostril three times a day for 7 days, subjects randomized to the group 2 took Vibrocil at the same dose and treatment regimen.

SUBJECTS Seventy-one subjects randomized (95.

3 of six subjects randomized to medical therapy.

Subjects randomized to the BPS intervention were 7.

Subjects randomized to the intervention arm will undergo percutaneous, ultrasound- (or MRI-) guided cryoablation with concurrent research core biopsy 7-10 days prior to surgery, and will receive a pre-operative infusion with ipilimumab at the dose of 1mg/kg IV, and nivolumab 240mg flat dose IV (1 to 5 days prior to cryoablation).

The mandated MPP parameters (eg, MPP‐AS) are programmed to subjects randomized to the MPP arm.

Results Among subjects randomized to BDET + MM, the overall number with normalized tympanograms and ETDQ-7 scores (Eustachian Tube Dysfunction Questionnaire–7) remained comparable to those reported at 6- versus 52-week follow-up: tympanograms, 73 of 143 (51.

MethodsA randomized, prospective, open-label, four-arm pilot study was conducted on 60 healthy adult subjects randomized to different fish oil supplement administration methods with (1) milk, (2) food, (3) an empty stomach, and (4) frozen capsules prior to ingestion.

Subjects randomized to sham had their devices activated after the primary endpoint at 12 weeks.

Results: Thirty-two subjects randomized, 30 completed the study (n = 11 control, n = 19 intervention), 57% female.

Subjects randomized to CAR switched to DTG+RPV at Week 52 (Late Switch (LS) DTG+RPV group) and change from LS Baseline (i.

Subjects randomized to the treatment arm were discharged home with the ReDS fluid monitor system and managed using ReDS measurements, according to protocol-defined algorithms.

This study aimed to compare self‐reported with objective measurements of energy intake changes (∆EI) during a 1‐year weight‐loss intervention with subjects randomized to low‐carbohydrate versus low‐fat diets.

METHODS Novel proteomic technologies were applied to examine 188 serum and plasma proteins from 40 CF subjects randomized to azithromycin in the AZ0004 trial.

We studied alanine and aspartate aminotransferase (ALT and AST) in subjects randomized to placebo who completed assessments over 36 mo in a cardiovascular outcome trial [the Stabilisation of Atherosclerotic Plaque by Initiation of Darapladib Therapy ("STABILITY") trial; n = 4,264; mean age: 64.

Phase two included 9 subjects randomized to 5-day supply of once-daily oral esomeprazole 20 mg, lansoprazole 15 mg, or omeprazole 20 mg.

RESULTS Subjects randomized were 39:13:39:13:38:13 in the respective groups, and 1 subject in the 8-weeks fluorometholone group was withdrawn.

Results: Of the 30 subjects randomized, 29 completed all 3 treatment periods.

Methods Twenty-two SCI subjects randomized into either a TRT + RT (n = 11) or TRT (n = 11) intervention for 16 wk.

Subjects randomized to the resistance training groups were required to perform whole-body strength training exercises 3-5 days a week for 12 weeks.

METHODS In a laboratory setting, healthy participants were assigned to one of four conditions in a between-subjects randomized factorial trial.

Four single ascending‐dose cohorts (10 mg, 30 mg, 60 mg, and 120 mg) and 3 multiple ascending‐dose cohorts (30 mg, 60 mg, and 120 mg once weekly for 4 weeks) each comprised 6 subjects randomized to GSK3389404 and 2 subjects randomized to placebo.

Healthy 14–17-year-olds underwent a within-subjects randomized protocol including 5-night spans of extended versus short sleep.

ResultsOf 130 subjects randomized, 118 had evaluable data (55 in the control and 63 in the treatment groups), 89% in both groups were adjudicated to have primarily AHF.

The trial was initiated on August 14, 2017, with 195 subjects randomized by October 5, 2018.

Subjects randomized to statin were significantly more likely to experience a rise in plasma interleukin-18 levels.

More subjects randomized to the ERAS protocol reported breastfeeding at discharge, 67.

Results Of 220 subjects randomized, 103 patients in each arm had sufficient data for analysis.

GLOW was a multicenter, double-blind, placebo-controlled pivotal study with subjects randomized to 2.

This study utilized a one-group within-subjects randomized design.

Subjects randomized to postconditioning experienced more favorable remodeling over 1 year (LV end-diastolic volume =157±34 to 150±38 mL) compared with the control group (157±40 to 165±45 mL; P<0.

Methods: We compared echocardiographic indices of RV, neoaortic, and tricuspid valve size and function at 14 months, pre-Fontan, and 6 years in 241 subjects randomized to a Norwood procedure using either the modified Blalock-Taussig shunt or RV-to-pulmonary-artery shunt.

For subjects randomized to T-DM1, the treatment will be in accordance with the approved label.

Four randomized, controlled, open-label, three-arm parallel group reduced exposure clinical studies have been conducted with subjects randomized to three arms: switching from cigarettes to THS 2.

Two between-subjects randomized controlled experiments were conducted with 42 and 34 participants.