• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Planning the duration of a comparative clinical trial with loss to follow-up and a period of continued observation.

作者信息

Rubinstein L V, Gail M H, Santner T J

出版信息

J Chronic Dis. 1981;34(9-10):469-79. doi: 10.1016/0021-9681(81)90007-2.

DOI:10.1016/0021-9681(81)90007-2
PMID:7276137
Abstract
摘要

相似文献

1
Planning the duration of a comparative clinical trial with loss to follow-up and a period of continued observation.规划一项存在失访及持续观察期的比较性临床试验的持续时间。
J Chronic Dis. 1981;34(9-10):469-79. doi: 10.1016/0021-9681(81)90007-2.
2
Planning the duration of accrual and follow-up for clinical trials.
J Chronic Dis. 1985;38(12):1009-18. doi: 10.1016/0021-9681(85)90099-2.
3
Sample size estimation for non-inferiority trials of time-to-event data.事件发生时间数据非劣效性试验的样本量估计
Pharm Stat. 2008 Oct-Dec;7(4):236-44. doi: 10.1002/pst.292.
4
Planning the size of survival time clinical trials with allowance for stratification.考虑分层因素来规划生存时间临床试验的规模。
Stat Med. 1988 May;7(5):559-69. doi: 10.1002/sim.4780070503.
5
Nonparametric estimation of duration of accrual and total study length for clinical trials.临床试验中累积期和总研究时长的非参数估计
Biometrics. 1987 Dec;43(4):903-12.
6
Logistics and management of clinical trials.临床试验的后勤保障与管理
Br J Clin Pharmacol. 1982 Jul;14(1):25-30. doi: 10.1111/j.1365-2125.1982.tb04930.x.
7
Adequacy of 6-month follow-up in chemotherapy trials.
Int J Tuberc Lung Dis. 2010 Jul;14(7):927; author reply 928.
8
Long-term follow-up of lipid-lowering trials.降脂试验的长期随访
Curr Opin Lipidol. 2015 Dec;26(6):572-9. doi: 10.1097/MOL.0000000000000230.
9
How to design a clinical in cardiology. The main issues.
Rev Port Cardiol. 2006 Jan;25(1):105-18.
10
Drug trials in myocardial infarction. Lessons to be learned from the Anturane Reinfarction Trial.
Eur J Clin Pharmacol. 1980 Jun;17(6):401-7. doi: 10.1007/BF00570155.

引用本文的文献

1
Using non-inferiority test of proportions in design of randomized non-inferiority trials with time-to-event endpoint with a focus on low-event-rate setting.在具有事件发生时间终点的随机非劣效性试验设计中,使用比例的非劣效性检验,重点关注低事件率情况。
Clin Trials. 2025 Apr;22(2):131-141. doi: 10.1177/17407745241284786. Epub 2024 Oct 12.
2
Freely accessible software for recruitment prediction and recruitment monitoring of clinical trials: A systematic review.用于临床试验招募预测和招募监测的免费软件:一项系统综述。
Contemp Clin Trials Commun. 2024 Apr 22;39:101298. doi: 10.1016/j.conctc.2024.101298. eCollection 2024 Jun.
3
Predicting Phase 1 Lymphoma Clinical Trial Durations Using Machine Learning: An In-Depth Analysis and Broad Application Insights.
使用机器学习预测1期淋巴瘤临床试验持续时间:深入分析与广泛应用洞察
Clin Pract. 2023 Dec 29;14(1):69-88. doi: 10.3390/clinpract14010007.
4
Clinical course of non-alcoholic fatty liver disease and the implications for clinical trial design.非酒精性脂肪性肝病的临床病程及其对临床试验设计的影响。
J Hepatol. 2022 Nov;77(5):1237-1245. doi: 10.1016/j.jhep.2022.07.004. Epub 2022 Jul 16.
5
On the design and the analysis of stratified biomarker trials in the presence of measurement error.存在测量误差时分层生物标志物试验的设计与分析。
Stat Med. 2021 May 30;40(12):2783-2799. doi: 10.1002/sim.8928. Epub 2021 Mar 16.
6
Concept and development of an interactive tool for trial recruitment planning and management.交互式试验招募规划和管理工具的概念和开发。
Trials. 2021 Mar 6;22(1):189. doi: 10.1186/s13063-021-05112-z.
7
Group sequential design for historical control trials using error spending functions.基于误差消耗函数的历史对照试验的分组序贯设计。
J Biopharm Stat. 2020 Mar;30(2):351-363. doi: 10.1080/10543406.2019.1684305. Epub 2019 Nov 12.
8
Milestone prediction for time-to-event endpoint monitoring in clinical trials.临床试验中事件发生时间终点监测的里程碑预测。
Pharm Stat. 2019 Jul;18(4):433-446. doi: 10.1002/pst.1934. Epub 2019 Feb 26.
9
Development of a genetic sensor that eliminates p53 deficient cells.开发一种能消除 p53 缺陷细胞的遗传传感器。
Nat Commun. 2017 Nov 13;8(1):1463. doi: 10.1038/s41467-017-01688-w.
10
Group Sequential Survival Trial Design and Monitoring Using the Log-Rank Test.使用对数秩检验的序贯生存试验设计与监测
Stat Biopharm Res. 2017;9(1):35-43. doi: 10.1080/19466315.2016.1189355. Epub 2017 Mar 2.