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临床试验/NCT01862406
NCT01862406已完成不适用

The Impact of Generic Labels on Consumption Dosage and Medication Compliance

Universidade Federal de Santa Catarina0 个研究点目标入组 101 人开始时间: 2010年10月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
101
主要终点
Non-Compliance

研究概览

简要总结

Although generic drugs are pharmacologically equivalent to their brand-name counterparts, prejudices against the former remain strong among patients and doctors. In a randomized controlled field experiment, this research assesses the extent to which generic (versus brand-name) labels affect patients' consumption dosage, medication compliance and reported pain.

详细描述

One hundred one patients scheduled to undergo invasive dental surgeries (i.e., dental implants) participated in the experiment. After dental surgery, patients were prescribed a once-daily analgesic regimen for up to 7 days. The intervention consisted of label manipulation. Patients were randomly assigned to either the brand-name analgesic or to its (purportedly) cheaper generic version. In reality, all participants obtained the same brand-name medication. The medication was provided at no cost, and patients were instructed to take the first pill while at the clinic. They were informed that they could (a) increase the dosage of the prescribed analgesic to twice daily if necessary and (b) stop taking the medication when no longer needed. Any other changes to the regimen were discouraged, and patients were instructed to consult with the dentist before any such changes. Telephone follow-ups were conducted at 24 hours, 4 days, and 7 days after surgery. Two main dependent variables were obtained: the number of prescribed analgesics consumed and the number of non-prescribed analgesics consumed. The patients also reported the pain felt during the period.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients scheduled to undergo dental implants and/or bone graft surgeries at the UFSC dental clinic

排除标准

  • •Patients not scheduled to undergo these treatments

研究组 & 干预措施

Brand-name Label

Active Comparator

actual brand-name analgesic presented

干预措施: Label (Other)

Generic Label

Experimental

Purportedly generic version of the analgesic presented

干预措施: Label (Other)

结局指标

主要结局

Non-Compliance

时间窗: 4 days after the intervention

Number of patients who consumed at least one non-prescribed analgesic pill during the period (from day 2 to day 4)

Non-compliance

时间窗: 7 days after the intervention

Number of patients who consumed at least one non-prescribed analgesic pill during the period (from day 5 to day 7)

Non-Compliance

时间窗: 1 day after the intervention

Number of patients who consumed at least one non-prescribed analgesic pill during the first 24 hours

次要结局

  • Consumption Dosage(4 days after the intervention)
  • Consumption dosage(7 days after the intervention)
  • Consumption Dosage(1 day after the intervention)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Marco Aurelio Bianchini

Associate Professor of Dentistry

Universidade Federal de Santa Catarina

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