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1 ts, tortuous vessels, and blood vessels with blind ends.
3 sively branched relative to controls, formed blind-ended 'bulbs' filled with mitochondria, and were s
5 d primarily in the suprachoroidea, and their blind-ended capillary branches enter the choriocapillari
6 /+) retinas displayed an increased number of blind-ended capillary sprout tips (P < 0.02) and endothe
8 ened and/or curly tail, no genital tubercle, blind-ended colons, hydronephrotic kidneys, and no bladd
9 ne with a large-diameter cell body, a large, blind-ending dendrite, and a giant ovoid, axon measuring
11 unanticipated finding was the influence of a blind-end microvessel on model convergence, indicating a
12 ureters and hence absent homolateral kidney; blind ending (obstructed) ipsilateral hemivagina and ces
14 open-label, randomized, crossover study with blind end point evaluation to compare the efficacy and s
15 uster (hospital-level) randomized open-label blinded end point (PROBE) clinical trial using a multice
16 open-label, randomized-controlled trial with blinded end point adjudication in intensive care unit-le
17 randomized, single-blind, 24-week study with blinded end point assessment among anemic (average hemog
21 PARTICIPANTS: Prospective, randomized, open-blinded end point clinical trial in 7 hospitals across A
23 t, pragmatic, prospective, randomized, open, blinded end point controlled trial conducted in 12 Spani
24 enter clinical trial of parallel groups with blinded end point design conducted in 24 teaching hospit
25 p, open-label randomized clinical trial with blinded end point evaluation conducted at 19 centers in
26 al was a multicenter randomized, open-label, blinded end point evaluation that enrolled 408 patients
27 llel-group, open-label treatment trials with blinded end point evaluation that met inclusion criteria
28 SETTING, AND PARTICIPANTS: This open-label, blinded end point randomized clinical trial was conducte
29 multicenter, prospective, randomized, open, blinded end point superiority clinical trial conducted a
31 ulticentre prospective randomized open-label blinded end point trial of combination beta-adrenergic r
32 -group, prospective, randomized, open-label, blinded end point trial, consenting patients with type 2
33 In this prospective, randomized, open-label, blinded end point trial, in a single UK hospital, 220 wo
34 open-label randomized clinical trial with a blinded end point was conducted from August 10, 2019, to
35 initiated PROBE (prospective randomized open blinded end point) outcome assessment trial, randomized
36 linical trial, with open-label treatment and blinded end point, conducted from February 2, 2018, to J
37 hrough May 31, 2018, this prospective, open, blinded end point, parallel-group randomized clinical tr
38 G, AND PARTICIPANTS: Randomized, open-label, blinded end point, phase 2, futility clinical trial that
39 ternational, multicentre, prospective, open, blinded end point, randomised controlled trials of patie
40 CIPANTS: This was a multicenter, open-label, blinded end point, randomized clinical trial conducted a
42 G, AND PARTICIPANTS: Randomized, open-label, blinded, end point trial set in a single hospital in the
43 SIGN, SETTING, AND PARTICIPANTS: Open-label, blinded-end point, bayesian-adaptive randomized trial wi
45 (ASTER) study was a randomized, open-label, blinded end-point clinical trial conducted in 8 comprehe
46 G, AND PARTICIPANTS: Randomized, open-label, blinded end-point clinical trial including 160 patients
49 hase 2, prospective, randomised, open-label, blinded end-point evaluation study, adults with supraten
50 lel-group, open-label treatment trial with a blinded end-point evaluation to compare GA with CS for t
54 sed, randomized, noninferiority, open-label, blinded end-point study at 34 stroke units using the Swe
55 center, prospective, randomized, open-label, blinded end-point trial, patients with breast cancer and
56 ) was an investigator-initiated, open-label, blinded end-point, randomized clinical trial with a 2 x
57 NG, AND PARTICIPANTS: Randomized, open-label blinded-end-point trial enrolling 788 patients hospitali
58 This trial was a prospective, randomized, blinded end-points study in patients >=75 years of age w
61 epithelium mimicking geographic atrophy, the blinding end-stage condition characteristic of the dry f
64 surface by a radial channel which becomes a blind-ended tunnel in the tetramer, and probably acts as
65 (pre-existing vessels, angiogenic plexus and blind-ended vessels (BEVs)) was quantified using in vivo