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ACTION IMPACT XXIV Pragmatic and Comparative Effectiveness Clinical Trials of Pain Treatments October 23, 2020A Matter of Record (301) 8904188MinUScript with Word Indexation IMPACT XXIV Pragmatic
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01
Determine the research question and objectives of the pragmatic trial.
02
Define the eligibility criteria for participants in the trial.
03
Decide on the intervention and comparator to be used in the trial.
04
Develop a protocol outlining the study design, methods, and procedures.
05
Obtain ethical approval and any necessary regulatory permissions for the trial.
06
Recruit and enroll participants according to the eligibility criteria.
07
Randomize participants to the intervention and comparator groups.
08
Collect data on outcomes and analyze the results to draw conclusions.
09
Publish and disseminate the findings of the pragmatic trial.

Who needs pragmatic trials of pain?

01
Researchers looking to evaluate the real-world effectiveness of pain treatments.
02
Healthcare providers seeking evidence-based guidelines for treating patients with pain.
03
Policymakers interested in implementing cost-effective interventions for pain management.
04
Patients and advocacy groups advocating for improved access to effective pain relief options.
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Pragmatic trials of pain are clinical trials designed to evaluate the real-world effectiveness of pain management interventions.
Researchers and sponsors conducting clinical trials related to pain management are required to file pragmatic trials of pain.
Pragmatic trials of pain are typically filled out using standardized forms provided by regulatory authorities or ethics committees.
The purpose of pragmatic trials of pain is to provide evidence on the effectiveness and safety of pain management interventions in real-world clinical settings.
Information such as study objectives, methods, participants, interventions, outcomes, and adverse events must be reported on pragmatic trials of pain.
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