Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT04432259

Oral Dexamethasone as an Intervention for Postoperative Pain and Nausea Management in Total Knee Arthroplasty

Status
Not Yet Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
300 (estimated)
Sponsor
Henry Ford Health System · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study aims to determine if oral dexamethasone provides clinically significant improvement in postoperative outcomes, specifically nausea and pain scores.

Detailed description

Protocols in perioperative pain management during total joint arthroplasty (TJA) have contributed to early discharge after surgery. As practices move to favor ambulatory surgery in total joint arthroplasty changes must be made to postoperative pain and nausea management. Spinal anesthesia has been essential in managing associated ambulatory TJA, however, nausea and vomiting are known detrimental side effects. The use of systemic steroids has also been shown in the literature to reduce pain scores, length of stay, the need for antiemetics, and increase the distance of ambulation without increasing the rate of surgical site infection or prosthetic joint infection. As more same-day total joint replacement is incorporated into practice, an oral alternative may prove beneficial.

Conditions

Interventions

TypeNameDescription
DRUGDexamethasone4 mg bid for 4 days
DRUGPlacebooral placebo

Timeline

Start date
2020-07-01
Primary completion
2022-06-01
Completion
2022-12-01
First posted
2020-06-16
Last updated
2020-06-16

Source: ClinicalTrials.gov record NCT04432259. Inclusion in this directory is not an endorsement.