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NCT03577730 · ClinicalTrials.gov registry record · Early Phase 1
Caffeine and Neurologic Recovery Following Surgery and General Anesthesia
A Early Phase 1 study of Pain, Postoperative, sponsored by University of Michigan.
- Completed
- Registry status
- Early Phase 1
- Development phase
- 71
- Enrollment target
- 1
- Study location
NCT03577730 is a Early Phase 1 study of Pain, Postoperative that has completed, run by University of Michigan. The registered enrollment target is 71 participants, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (74% lower). The trial reports 1 study location across 1 state.
The verdict
NCT03577730, a Early Phase 1 study of Pain, Postoperative, has completed, sponsored by University of Michigan.
- COMPLETED
- Registry status
- Early Phase 1
- Development phase
- 71 participants
- Enrollment target
- 1
- Study location
Study Summary
The ongoing opioid epidemic is a public health crisis, and surgical patients are particularly vulnerable to opioid-dependency and related risks. Emerging data suggest that caffeine may reduce pain after surgery. Thus, the purpose of this study is to test whether caffeine reduces pain and opioid requirements after surgery. The investigators will also test whether caffeine improves mood and brain function (e.g., learning, memory) after surgery.
Conditions Studied
Interventions
- DRUG Dextrose Water
- DRUG Caffeine Citrate
Study Locations (1)
Michigan
- Michigan Medicine - Ann Arbor
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 71 participants |
| Start Date | 2018-07-10 |
| Est. Completion | 2020-01-17 |
| Phase | Early Phase 1 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03577730
The ClinicalTrials.gov registry entry for NCT03577730 describes a study currently listed as completed, categorized as Early Phase 1. The registered enrollment target is 71 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (74% lower). The listed sponsor is University of Michigan, which has 1,327 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Pain, Postoperative appearing as the primary indexed condition, and to 2 interventions - of which Dextrose Water is the first listed.
NCT03577730 reports 1 study location spanning 1 distinct geographic area - top geographies include Michigan.
Frequently Asked Questions
What is clinical trial NCT03577730 about?
NCT03577730 is a clinical study titled "Caffeine and Neurologic Recovery Following Surgery and General Anesthesia". The ongoing opioid epidemic is a public health crisis, and surgical patients are particularly vulnerable to opioid-dependency and related risks. Emerging data suggest that caffeine may reduce pain after surgery. Thus, the purpose of this study is to test whether caffeine reduces pain and opioid requ...
What is the current status of trial NCT03577730?
This trial is currently completed. It is a Early Phase 1 study. The enrollment target is 71 participants. The study started on 2018-07-10. Estimated completion is 2020-01-17.
What conditions does trial NCT03577730 study?
This clinical trial studies the following conditions: Pain, Postoperative.
What interventions are being tested in trial NCT03577730?
The interventions under investigation include: Dextrose Water (DRUG), Caffeine Citrate (DRUG).
Who is sponsoring clinical trial NCT03577730?
This trial is sponsored by University of Michigan, which has 1,327 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03577730 being conducted?
This trial has 1 study location across Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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