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临床试验/NCT02051296
NCT02051296已完成2 期

A Trial of Minocycline for Pain After Carpal Tunnel and Trigger Release

VA Palo Alto Health Care System1 个研究点 分布在 1 个国家目标入组 131 人开始时间: 2012年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
131
试验地点
1
主要终点
Time to Pain Resolution

研究概览

简要总结

The investigators are looking at whether peri-operative minocycline will reduce the duration of pain after minor hand surgery: carpal tunnel release and trigger finger release.

The investigators' hypothesis is that minocycline will reduce post-operative pain.

详细描述

This is a double blinded randomized controlled trial. Patients are given 100mg of minocycline 2 hours prior to their procedure and then 100mg two times a day for 5 days. The subjects are then contacted daily to check their level of pain. The investigators' outcome of interest is time to pain resolution.

The investigators will perform a futility analysis to assess if a larger trial would be a reasonable next step after this pilot study.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult, Veteran,

排除标准

  • Kidney failure, Liver failure, thrombocytopenia, ALS, SLE, Frailty, unable to understand survery

研究组 & 干预措施

minocycline

Experimental

perioperative minocycline for 5 days, starting 2 hours prior to surgery then 100mg BID

干预措施: Minocycline (Drug)

Placebo

Placebo Comparator

PLacebo

干预措施: placebo (Drug)

结局指标

主要结局

Time to Pain Resolution

时间窗: up to 365 days

the time until patient answers no pain at surgical site for three consecutive days

次要结局

未报告次要终点

研究者

发起方
VA Palo Alto Health Care System
申办方类型
Fed
责任方
Principal Investigator
主要研究者

Catherine Curtin

Staff Physician

VA Palo Alto Health Care System

研究点 (1)

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