Back to Authors

Chaturvedi, Seemant

https://orcid.org/0000-0001-8660-7644

Mayo Clinic

University of Maryland, Baltimore

Citations 26

Factors Associated With Time to Site Activation, Randomization, and Enrollment Performance in a Stroke Prevention Trial
Brown, Robert D. , Roubin, Gary S., Howard, Virginia J. , Cesko, Eldina, Barrett, Kevin M. , Longbottom, Mary, Voeks, Jenifer H. , Brott, Thomas G. , Lal, Brajesh K. , Howard, George , Longbottom, Mary E, Demaerschalk, Bart M. , Chaturvedi, Seemant , Meschia, James F. , Howard, Virginia J , Howard, George

Stroke | August 3, 2017 | Volume: 48 | Issue: 9 | Pages: 2511-2518

10.1161/strokeaha.117.016976 Get It

Background and Purpose— Multicenter clinical trials attempt to select sites that can move rapidly to randomization and enroll sufficient numbers of patients. However, there are few assessments of the success of site selection. Methods— In the CREST-2 (Carotid Revascularization and Medical Management for Asymptomatic Carotid Stenosis Trials), we assess factors associated with the time between site selection and authorization to randomize, the time between authorization to randomize and the first randomization, and the average number of randomizations per site per month. Potential factors included characteristics of the site, specialty of the principal investigator, and site type. Results— For 147 sites, the median time between site selection to authorization to randomize was 9.9 months (interquartile range, 7.7, 12.4), and factors associated with early site activation were not identified. The median time between authorization to randomize and a randomization was 4.6 months (interquartile range, 2.6, 10.5). Sites with authorization to randomize in only the carotid endarterectomy study were slower to randomize, and other factors examined were not significantly associated with time-to-randomization. The recruitment rate was 0.26 (95% confidence interval, 0.23–0.28) patients per site per month. By univariate analysis, factors associated with faster recruitment were authorization to randomize in both trials, principal investigator specialties of interventional radiology and cardiology, pre-trial reported performance >50 carotid angioplasty and stenting procedures per year, status in the top half of recruitment in the CREST trial, and classification as a private health facility. Participation in StrokeNet was associated with slower recruitment as compared with the non-StrokeNet sites. Conclusions— Overall, selection of sites with high enrollment rates will likely require customization to align the sites selected to the factor under study in the trial. Clinical Trial Registration— URL: http://www.clinicaltrials.gov . Unique identifier: NCT02089217.
Carotid revascularization and medical management for asymptomatic carotid stenosis: Protocol of the CREST-2 clinical trials
Howard, Virginia J. , Lal, Brajesh K. , Turan, Tanya N. , Roubin, Gary S., Brown, Robert D. , Voeks, Jenifer H. , Barrett, Kevin M. , Lazar, Ronald M. , Moore, Wesley S. , Wadley, Virginia G. , Moy, Claudia S., Chimowitz, Marc I. , Howard, George , Brott, Thomas G. , Meschia, James F. , Demaerschalk, Bart M. , Huston, John , Chaturvedi, Seemant , Howard, Virginia J , Howard, George

International Journal of Stroke | May 2, 2017 | Volume: 12 | Issue: 7 | Pages: 770-778

10.1177/1747493017706238 Get It

Rationale Trials conducted decades ago demonstrated that carotid endarterectomy by skilled surgeons reduced stroke risk in asymptomatic patients. Developments in carotid stenting and improvements in medical prevention of stroke caused by atherothrombotic disease challenge understanding of the benefits of revascularization. Aim Carotid Revascularization and Medical Management for Asymptomatic Carotid Stenosis Trial (CREST-2) will test whether carotid endarterectomy or carotid stenting plus contemporary intensive medical therapy is superior to intensive medical therapy alone in the primary prevention of stroke in patients with high-grade asymptomatic carotid stenosis. Methods and design CREST-2 is two multicenter randomized trials of revascularization plus intensive medical therapy versus intensive medical therapy alone. One trial randomizes patients to carotid endarterectomy plus intensive medical therapy versus intensive medical therapy alone; the other, to carotid stenting plus intensive medical therapy versus intensive medical therapy alone. The risk factor targets of centrally directed intensive medical therapy are LDL cholesterol <70 mg/dl and systolic blood pressure <140 mmHg. Study outcomes The primary outcome is the composite of stroke and death within 44 days following randomization and stroke ipsilateral to the target vessel thereafter, up to four years. Change in cognition and differences in major and minor stroke are secondary outcomes. Sample size Enrollment of 1240 patients in each trial provides 85% power to detect a treatment difference if the event rate in the intensive medical therapy alone arm is 4.8% higher or 2.8% lower than an anticipated 3.6% rate in the revascularization arm. Discussion Management of asymptomatic carotid stenosis requires contemporary randomized trials to address whether carotid endarterectomy or carotid stenting plus intensive medical therapy is superior in preventing stroke beyond intensive medical therapy alone. Whether carotid endarterectomy or carotid stenting has favorable effects on cognition will also be tested. Trial registration United States National Institutes of Health Clinicaltrials.gov NCT02089217
The urgent need for contemporary clinical trials in patients with asymptomatic carotid stenosis
Chimowitz, Marc I. , Brown, Robert D. , Lal, Brajesh K. , Chimowitz, Marc, Chaturvedi, Seemant , Meschia, James F.

Neurology | September 29, 2016 | Volume: 87 | Issue: 21 | Pages: 2271-2278

10.1212/wnl.0000000000003267 Get It

Carotid Endarterectomy for Asymptomatic Stenosis
Howard, George , Meschia, James, Chaturvedi, Seemant , Meschia, James F. , Howard, George

JAMA Internal Medicine | July 6, 2015 | Volume: 175 | Issue: 7 | Pages: 1241

10.1001/jamainternmed.2015.1118 Get It

Anticoagulants and antiplatelet agents in acute ischemic stroke [RETIRED]
Coull, Bruce M. , Williams, Linda S. , Heitzman, Daragh, Johnston, Karen C. , Starkman, Sidney , Wilterdink, Janet L., Goldstein, Larry B. , Meschia, James F. , Chaturvedi, Seemant , Morgenstern, Lewis B. , Levine, Steven R. , Saver, Jeffrey L.

Neurology | May 13, 2012 | Volume: 59 | Issue: 1 | Pages: 13-22

10.1212/wnl.59.1.13 Get It