Patient Controlled Administration of Liquid Acetaminophen
Recruiting
Phase 1
Interventional Study
Pain
Pain, Postoperative
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Trial phase
- Phase 1
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 24 (estimated)
- Sponsor
- Yale University · Other
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About This Trial
This is a proof of concept pilot study investigating the feasibility and acceptability of patient controlled oral medication administration, using the commonly used and low risk medication in the hospital, oral acetaminophen.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
Participants
* Adult patients older than 18 years old admitted to SRC for total shoulder and reverse total shoulder arthroplasty
Nurses
* The nurse who will administer acetaminophen to a study patient.
Exclusion Criteria:
Participants
* Pregnant patient
* Patients that can…
Contacts