Arthropathy of KneePhase 4DEXA_PERIOPNCT06715709
How Many Dexamethasone Doses Should Be Given Perioperatively?
A Phase 4 study testing Dexamethasone IV, Dexamethasone IV+Oral and Dexamethasone IV+Oral 2 Day in people with Arthropathy of Knee, run by Mayo Clinic at 1 site in United States.
Trial summary
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 Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Arthropathy of Knee
- What is being tested?
- Dexamethasone IV, Dexamethasone IV+Oral and Dexamethasone IV+Oral 2 Day
- Type of treatment
- Pill or oral medicine, Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 339 participants
- Where
- 1 siteUnited States
- Study dates
- 25 Mar 2025to 1 Jan 2027
- Phase
- Phase 4
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Age > 18 years
- Primary total knee arthroplasty
Who cannot join
- 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
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
United States1 site
Mayo Clinic in Rochester
Rochester, Minnesota, 55905
About this study
Official title: Corticosteroids in Total Knee Arthroplasty: How Many Dexamethasone Doses Should Be Given Perioperatively? A Randomized Controlled Trial
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
Read the detailed description
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
- Arthropathy of Knee
- Being tested
- Dexamethasone IV, Dexamethasone IV+Oral, Dexamethasone IV+Oral 2 Day
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Dexamethasone IVDrug
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.
Dexamethasone IV+OralDrug
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.
Dexamethasone IV+Oral 2 DayDrug
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.
| Study group | Role | What they receive |
|---|---|---|
| (1) dexamethasone administered intraoperatively at the time of anesthesia | Other | (1) dexamethasone administered intraoperatively at the time of anesthesia Receives: Drug: Dexamethasone IV |
| (2) dexamethasone administered intraoperatively and on the morning of the first postoperative day, | Experimental | (2) dexamethasone administered intraoperatively and on the morning of the first postoperative day, Receives: Drug: Dexamethasone IV+Oral |
| (3) dexamethasone administered intraoperatively, the morning of the first& second postoperative day | Experimental | (3) dexamethasone administered intraoperatively, the morning of the first postoperative day, and the morning of the second postoperative day. Receives: Drug: Dexamethasone IV+Oral 2 Day |
What is being measured
The primary outcome is the main question the study is designed to answer.
Opioid consumption
Cumulative opioid consumption within 72 hours after Total Knee Arthroplasty, measured in oral morphine milligram equivalents.
Measured: 72 hours
Secondary outcomes (1)
Sleeplesssness
Sleeplessness will be measured by recording the number of hours slept in a 24-hour period for 7 days postoperatively.
Measured: 7 days
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted4 Dec 2024
- Study start25 Mar 2025
- Primary completion1 Jan 2027 (estimated)
- Study completion1 Jan 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Arthropathy of KneeStudies of the same condition, open and under way.
- More trials run by Mayo ClinicThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 4
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Care provider
- Enrolment
- 339 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Mayo Clinic
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Charles P. Hannon, Mayo Clinic
- Investigators
- Charles Hannon, Principal investigator, Mayo Clinic
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06715709
- Sponsor's protocol ID
- 24-008239
- Acronym
- DEXA_PERIOP
- Status last verified
- Feb 2026
- First submitted
- 29 Nov 2024
- Last updated
- 6 Feb 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 6 Feb 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Corticosteroids in Total Knee Arthroplasty: How Many Dexamethasone Doses Should Be Given Perioperatively? A Randomized Controlled Trial
- ClinicalTrials.gov ID
- NCT06715709
- Acronym / sponsor ID
- DEXA_PERIOP / 24-008239
- Conditions
- Arthropathy of Knee
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Enrolling by invitation
- Enrolment
- 339 participants (estimated)
- Lead sponsor
- Mayo ClinicUniversity, hospital or other
- Study start
- 25 Mar 2025 (actual)
- Primary completion
- 1 Jan 2027 (estimated)
- Study completion
- 1 Jan 2027 (estimated)
- First posted
- 4 Dec 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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
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.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (care provider)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| (1) dexamethasone administered intraoperatively at the time of anesthesia | Other | Drug: Dexamethasone IV(1) dexamethasone administered intraoperatively at the time of anesthesia |
| (2) dexamethasone administered intraoperatively and on the morning of the first postoperative day, | Experimental | Drug: Dexamethasone IV+Oral(2) dexamethasone administered intraoperatively and on the morning of the first postoperative day, |
| (3) dexamethasone administered intraoperatively, the morning of the first& second postoperative day | Experimental | Drug: Dexamethasone IV+Oral 2 Day(3) dexamethasone administered intraoperatively, the morning of the first postoperative day, and the morning of the second postoperative day. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (2 listed)
- Age > 18 years
- Primary total knee arthroplasty
Key exclusion criteria (8 listed)
- Age < 18 year
- Revision or unicompartmental knee arthroplasty
- Corticosteroid use within 3 months prior to TKA
- Inflammatory arthritis
- Current systemic fungal infection
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Dexamethasone IVPatients 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. | Drug | (1) dexamethasone administered intraoperatively at the time of anesthesia |
| Dexamethasone IV+OralPatients 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. | Drug | (2) dexamethasone administered intraoperatively and on the morning of the first postoperative day, |
| Dexamethasone IV+Oral 2 DayPatients 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. | Drug | (3) dexamethasone administered intraoperatively, the morning of the first& second postoperative day |
Primary outcome
Opioid consumption
Time frame: 72 hours
Cumulative opioid consumption within 72 hours after Total Knee Arthroplasty, measured in oral morphine milligram equivalents.
1 secondary outcome
Sleeplesssness
Time frame: 7 days
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 Feb 2026.
- Individual participant dataSharing planned: No
Related trials for Arthropathy of Knee
RecruitingPhase 3
Phase 3 Pivotal Trial Comparing CARTISTEM® and Surgical Comparator for Knee Cartilage Lesions and Osteoarthritis
Knee Cartilage Defects
Recruiting
The Effect of Different Exercise Training Programs on Muscle Oxygenation in Individuals With Knee Osteoarthritis
Osteoarthritis of Knee
Not yet recruiting
Comparison of Telerehabilitation and Usual Rehabilitation After Knee or Hip Surgery
Orthopedic Surgery, Rehabilitation
Not yet recruiting
Comparison of High-Intensity and Conventional Physical Therapy in Musculoskeletal Disorders
Low Back Pain, Radicular Syndrome
Recruiting
Exploration of Appropriate BIS Range and Propofol Effect-site Concentration During Total Intravenous Anesthesia With Concomitant Adjuvants.
Knee Osteoarthritis, Replacement, Knee
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Charles Hannon principal investigator
Mayo Clinic
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 4 study testing Dexamethasone IV, Dexamethasone IV+Oral and Dexamethasone IV+Oral 2 Day in people with Arthropathy of Knee, run by Mayo Clinic at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: enrolling by invitation, as of the sponsor's last update on 6 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Opioid consumption (time frame: 72 hours). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Feb 2026.