How Many Dexamethasone Doses Should Be Given Perioperatively?

NCT ID: NCT06715709

Last Updated: 2025-04-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Clinical Phase

PHASE4

Total Enrollment

339 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-03-25

Study Completion Date

2027-01-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The purpose of this study is to determine the most efficient and safest dexamethasone dose given perioperatively during total knee arthroplasty that reduces postoperative option consumption and pain, improves postoperative nausea and vomiting, and minimizes postoperative complications

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Perioperative multimodal analgesia and anesthesia regimens have become the standard of care in modern total joint arthroplasty. This has been driven in part by an emphasis on decreasing postoperative opiate use, a growing trend towards shorter inpatient hospital stays and outpatient TKAs, and motivation to improve patient satisfaction after TKA. Acute postoperative pain not only decreases patient satisfaction,1 but can also lead to associated complications including chronic opioid use,2 disrupted sleep,3 and impaired early mobilization, which can prolong recovery and increase the risk of medical complications such as venous thromboembolism (VTE).4,5 Previously, opioids were the basis of pain management regimens, however, opioids may cause significant adverse events including nausea, vomiting, ileus, sedation, urinary retention, respiratory depression, and others, in addition to a risk of addiction.6 Conversely, contemporary arthroplasty relies on minimizing opiate use by administering multimodal analgesia and anesthesia that target various pain and inflammatory pathways7,8 to improve postoperative outcomes and facilitate rapid discharge postoperatively.

Corticosteroids are potent anti-inflammatory medications with anti-emetic properties,9,10 with previous studies demonstrating their effectiveness in reducing postoperative pain, nausea, and vomiting.9 Therefore, corticosteroids are commonly used in current multimodal pain management regimens. Dexamethasone is one of the most well-studied corticosteroids in the total joint arthroplasty literature. Previous randomized controlled trials evaluated the administration of multiple perioperative dexamethasone doses compared to one dose of perioperative dexamethasone and reported that multiple doses were associated with reduced opioid consumption and pain in the early postoperative period after TKA,11-13 while another reported no significant differences.14 Furthermore, while Xu et al. did not demonstrate a difference in postoperative nausea and vomiting between patients receiving one perioperative dexamethasone dose versus three doses,13 other RCTs reported that additional doses of dexamethasone was associated with significantly decreased postoperative nausea.11,12 This is important because postoperative nausea is a commonly cited adverse effect of anesthesia. The RCT by Xu et al. compared one dose to three doses of dexamethasone,13 while the RCTs by Backes et al., Wu et al., and Gasbjerg et al. compared one dose to two doses of dexamethasone in the setting of TKA.11,12,14 Following total hip arthroplasty, Lei et al. evaluated two doses of perioperative dexamethasone to three doses and reported that the three dose treatment arm had greater reductions in postoperative pain and nausea, greater range of motion, and shorter length of hospital stays, without any increase in adverse events.15 To our knowledge, there is no randomized controlled trial directly comparing multiple-dose treatment arms (i.e. one versus two versus three or more perioperative dexamethasone doses) in the setting of TKA. Therefore, the standard number of doses of dexamethasone that should be administered in the perioperative period has not been established.

Furthermore, concern remains regarding the theoretical adverse events that may be associated with corticosteroid administration, including decreased wound healing, increased risk of infection, or gastrointestinal hemorrhage.16,17 Previous studies investigating dexamethasone may have excluded patients with diabetes mellitus or poorly controlled diabetes mellitus due to concern that corticosteroids would increase blood glucose levels, thereby increasing the risk of medical complications or periprosthetic joint infection. However, while some studies have demonstrated corticosteroid use may lead to transient increases in blood glucose levels, recent studies have reported no difference in postoperative complication rates.13,18,19 Heterogeneity between studies, small sample sizes, and exclusion of at-risk groups, such as diabetic patients, limit many previous studies that reported on complications associated with corticosteroid use in total joint arthroplasty. Further research is required to characterize the safety profile of dexamethasone in patients receiving TKA.

The previous literature is heterogenous in the dose, number of doses, and timing of perioperative dexamethasone that was administered, in addition to a lack of standardization in the multimodal analgesia and anesthesia regimen. Therefore, the purpose of this study is to perform a multicenter randomized controlled trial to determine the optimal number of dexamethasone doses to be administered in the TKA perioperative period by comparing postoperative outcomes in patients receiving one, two, or three doses of intravenous dexamethasone.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Arthropathy of Knee

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Caregivers

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

(1) dexamethasone administered intraoperatively at the time of anesthesia

(1) dexamethasone administered intraoperatively at the time of anesthesia

Group Type OTHER

Dexamethasone IV

Intervention Type DRUG

Patients will receive dexamethasone administered intraoperatively at the time of anesthesia. The dose of dexamethasone will be 16mg intravenous (IV) if you do not have a prior diagnosis of diabetes mellitus, or 8mg IV if you do have a previous diagnosis of diabetes mellitus.

(2) dexamethasone administered intraoperatively and on the morning of the first postoperative day,

(2) dexamethasone administered intraoperatively and on the morning of the first postoperative day,

Group Type EXPERIMENTAL

Dexamethasone IV+Oral

Intervention Type DRUG

Patients will receive dexamethasone administered intraoperatively and on the morning of the first postoperative day. The dose of dexamethasone will be 16mg intravenous (IV) if you do not have a prior diagnosis of diabetes mellitus, or 8mg IV if you do have a previous diagnosis of diabetes mellitus. The medication will be intravenously administered while inpatient, and via oral route when discharged.

(3) dexamethasone administered intraoperatively, the morning of the first& second postoperative day

(3) dexamethasone administered intraoperatively, the morning of the first postoperative day, and the morning of the second postoperative day.

Group Type EXPERIMENTAL

Dexamethasone IV+Oral 2 Day

Intervention Type DRUG

Patients will receive dexamethasone administered intraoperatively, the morning of the first postoperative day, and the morning of the second postoperative day. The dose of dexamethasone will be 16mg intravenous (IV) if you do not have a prior diagnosis of diabetes mellitus, or 8mg IV if you do have a previous diagnosis of diabetes mellitus. The medication will be intravenously administered while inpatient, and via oral route when discharged.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Dexamethasone IV

Patients will receive dexamethasone administered intraoperatively at the time of anesthesia. The dose of dexamethasone will be 16mg intravenous (IV) if you do not have a prior diagnosis of diabetes mellitus, or 8mg IV if you do have a previous diagnosis of diabetes mellitus.

Intervention Type DRUG

Dexamethasone IV+Oral

Patients will receive dexamethasone administered intraoperatively and on the morning of the first postoperative day. The dose of dexamethasone will be 16mg intravenous (IV) if you do not have a prior diagnosis of diabetes mellitus, or 8mg IV if you do have a previous diagnosis of diabetes mellitus. The medication will be intravenously administered while inpatient, and via oral route when discharged.

Intervention Type DRUG

Dexamethasone IV+Oral 2 Day

Patients will receive dexamethasone administered intraoperatively, the morning of the first postoperative day, and the morning of the second postoperative day. The dose of dexamethasone will be 16mg intravenous (IV) if you do not have a prior diagnosis of diabetes mellitus, or 8mg IV if you do have a previous diagnosis of diabetes mellitus. The medication will be intravenously administered while inpatient, and via oral route when discharged.

Intervention Type DRUG

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Age \> 18 years
* Primary total knee arthroplasty

Exclusion Criteria

* Age \< 18 year
* Revision or unicompartmental knee arthroplasty
* Corticosteroid use within 3 months prior to TKA
* Inflammatory arthritis
* Current systemic fungal infection
* Renal or liver failure
* Prior adverse reaction to corticosteroid
* Primary TKA requiring hardware removal
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Mayo Clinic

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Charles P. Hannon

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Charles Hannon

Role: PRINCIPAL_INVESTIGATOR

Mayo Clinic

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Mayo Clinic in Rochester

Rochester, Minnesota, United States

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

United States

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Erin Hennessey

Role: CONTACT

507-284-1975

Gabe Schouten

Role: CONTACT

507-266-5895

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Erin Hennessey

Role: primary

507-284-1975

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

24-008239

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Steroids in Total Knee Arthroplasty
NCT02219581 TERMINATED PHASE4
Antibiotic Prophylaxis in High-Risk Arthroplasty Patients
NCT04297592 ENROLLING_BY_INVITATION PHASE4