PHASE I TRIAL OF QUINAPRIL IN PEDIATRIC HYPERTENSION

$0M01FY2001RRNIH

Baylor College Of Medicine, Houston TX

Investigators

Linked publications & trials

Paper 33526606 Paper 33381925 Paper 33328537 Paper 33234943 Paper 33055522 Paper 33035237 Paper 32582596 Paper 31876611 Paper 31744891 Paper 31303264 Paper 30206298 Paper 30201514 Paper 29724670 Paper 29557247 Paper 29470286 Paper 29315015 Paper 29311357 Paper 29048210 Paper 28943110 Paper 28918882 Paper 28868529 Paper 28825123 Paper 28736735 Paper 28486640 Paper 28399055 Paper 28383538 Paper 28209771 Paper 28012151 Paper 27929698 Paper 27916618 Paper 27567561 Paper 27238578 Paper 27238356 Paper 27196378 Paper 27018579 Paper 26851065 Paper 26807434 Paper 26802570 Paper 26586473 Paper 26544725 Paper 26296711 Paper 26241705 Paper 26226992 Paper 26075429 Paper 25999776 Paper 25915190 Paper 25906753 Paper 25753424 Paper 25742612 Paper 25730293 Paper 25714579 Paper 25670824 Paper 25641242 Paper 25635121 Paper 25556022 Paper 25503497 Paper 25488688 Paper 25431212 Paper 25376399 Paper 25301036 Paper 25171870 Paper 25144778 Paper 25086207 Paper 25068253 Paper 25042691 Paper 25020112 Paper 24978596 Paper 24965231 Paper 24746253 Paper 24654704 Paper 24635646 Paper 24630270 Paper 24535626 Paper 24530202 Paper 24496312 Paper 24491361 Paper 24467569 Paper 24463451 Paper 24406073 Paper 24360992 Paper 24311632 Paper 24253285 Paper 24189578 Paper 24184574 Paper 24144944 Paper 24115918 Paper 24081740 Paper 24050698 Paper 24030379 Paper 24002093 Paper 23992748 Paper 23956055 Paper 23885357 Paper 23880316 Paper 23796525 Paper 23775211 Paper 23750510 Paper 23718573 Paper 23712984 Paper 23690521

Abstract

a.) Objective of this Research: The purpose of this study is to investigate the safety, efficacy and dose response of quinapril, an ACE inhibitor, in the treatment of children ages 5 to 16 with hypertension. b.) Study Design: This is a double-blind, placebo-controlled, parallel group, randomized design. A 10 to 14 day, single-blind, placebo lead-in phase followed by stratification, based on weight into 1 of 2 strata. Each stratum will include 4 treatment groups, a 2-week blinded treatment phase and a 6-week blinded extension. The study medication will be dispensed in pill form.

View original record on NIH RePORTER →