ライフサイエンスコーパス: study protocol

1 t baseline shock (for whom fluid balance was managed by the study protocol).

2 virus vaccine, and provided a blood sample according to the study protocol).

3 All analyses were prespecified in the study protocol.

4 up at 6 months (LTFU) was listed as the main outcome in the study protocol.

5 Thirty-six patients completed the study protocol.

6 Safety analyses included all treated patients, as per study protocol.

7 This study analysis was specified in the study protocol.

8 Of 174 patients, 144 completed the study protocol.

9 atients were examined by the same team following a detailed study protocol.

10 eam successfully refined and implemented a patient-centered study protocol.

11 Ethics Committee at Hopital Albert Schweitzer approved the study protocol.

12 We describe the study protocol.

13 All participants completed the study protocol.

14 and established antimicrobial susceptibility using standard study protocols.

15 A standardized study protocol, 150 Nocardia isolates, and NIH and OSU Nocard

16 ts were followed for 3.1 +/- 1.5 years and 82 completed the study protocol 5-year visit.

17 8%) patients completed the prophylaxis, 10 discontinued the study protocol: 6 for infusion-related AE, 4 for suspected IF

18 Patients completed prescribed study protocol and follow-up.

19 n on study design, recruitment procedures and outcomes from study protocols and annual reports, and in-depth interviews w

20 The institutional review board approved the study protocol, and informed consent was obtained from all pa

21 Analyses were powered according to the original study protocol, and we analysed FKSI-DRS and EQ-5D data for a

22 Each institutional review board approved the prospective study protocol, and written informed consent was obtained.

23 In accordance with the retrospective study protocol approved by the institutional review board, 22

24 This study protocol describes the design of the first randomized c

25 Lack of experience in study protocol development and/or data analysis was associate

26 Inclusion of nurses in study protocol development, improved communication of study p

27 he methods and results of health research are documented in study protocols, full study reports (detailing all analyses),

28 The study protocol has been registered with PROSPERO, number CRD4

29 /- 2.2 years, BMI 25.1 +/- 1.0 kg/m(2)) participated in two study protocols in random order over two consecutive days.

30 subjects; n=14) complex ventricular arrhythmias underwent a study protocol including contrast-enhanced cardiac magnetic r

31 All participants were followed through the initial study protocol of 24 months and were approached to enter an e

32 The Lithuanian Regional Ethics Committee approved the study protocol (permission No.

33 We discuss the study protocol regarding pediatric CTU examinations.

34 Current clinical study protocols rely on the ex vivo expansion of donor T reg

35 The study protocol specified preinjection preparation to include

36 A surgeon feedback form was recorded as part of the study protocol to answer specific questions regarding intraop

37 nt at the primary endpoint, timing of delivery based on the study protocol using late changes in the DV waveform might pr

38 On May 30, 2012, the study protocol was amended to allow crossover from control to

39 On Sept 12, 2012, the study protocol was amended to allow patients with disease pro

40 en informed consent was obtained from all patients, and the study protocol was approved by the committee on human researc

41 en informed consent was obtained from all patients, and the study protocol was approved by the institutional committee on

42 en informed consent was obtained from all patients, and the study protocol was approved by the institutional ethical comm

43 Materials and Methods The study protocol was approved by the institutional review board

44 This study protocol was approved by the institutional review board

45 Materials and Methods The study protocol was approved by the local ethics committee.

46 The study protocol was completed by 51% of enrolled patients.

47 A study protocol was finalized before data collection.

48 Using a laboratory study protocol, we show that SD individuals can maintain info

49 approach to determining eligibility criteria for individual study protocols, which may help guide future investigators an

50 irty-seven eyes of 37 patients were enrolled in the initial study protocol, with 19 eyes randomized to fresh and 18 to fr