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Effect of Methylprednisolone on Immune Signaling in Hip-arthroplasty Patients

Effect of Preoperative Intravenous High Dose Methylprednisolone on Immune Signaling in Patients Scheduled for Total Hip-arthroplasty

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02542592
Enrollment
64
Registered
2015-09-07
Start date
2015-09-30
Completion date
2017-01-31
Last updated
2017-01-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteoarthrosis

Keywords

Glucocorticoids, Immune Signaling, Recovery, Hip arthroplasty, total

Brief summary

The study evaluates the pathophysiological effects of a single dose Methylprednisolone administered prior to total hip-arthroplasty (THA) surgery. The investigators examine the effect on immune signaling and recovery after surgery. Half of participants will receive intravenous Solu-Medrol 125 mg, while the other half will receive placebo. The investigators hypothesize that the group receiving Methylprednisolone will experience a positive modulation of the immune response and an enhanced recovery.

Detailed description

The anti-inflammatory effects of glucocorticoids are well known. The beneficial effects on postoperative pain, postoperative nausea and vomiting are well-documented. Hip-arthroplasty surgery and the inflammatory stress response in general affect the potential of recovery. The basic physiological mechanisms behind restoration of recovery after surgery are still unresolved. The many different immune cells involved in the complex signal response enables wound healing and recovery, and the individual immune signal pattern might be able to predict recovery. The effects of glucocorticoids on this immune signal pattern is unknown and calls for further investigation. The study is to be considered as exploratory. This study is embedded in a primary study registrated as: NCT02445898 For further details please view the EudraCT registration: EudraCT nr.: 2015-000102-19

Interventions

DRUGMethylprednisolone

Comparison of preoperative single high dose of Methylprednisolone 125 mg iv. and isotonic Sodium Chloride (placebo)

Sponsors

Bispebjerg Hospital
CollaboratorOTHER
Rigshospitalet, Denmark
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
55 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Osteoarthrosis * Undergoing total unilateral hip-arthroplasty surgery * Speak and understand Danish * Have given informed content

Exclusion criteria

* Revision or bilateral hip-arthroplasty surgery * General anaesthesia * Allergy or intolerance towards Methylprednisolone * Local or systemic infection * Permanent systemic treatment with steroids within 30 days peroperatively * Insulin-dependent diabetes * Atrial fibrillation * Neurological disease incl. Parkinsons * Daily use of hypnotics or sedatives * Alcohol abuse \>35 units per week * Active treatment of ulcer within 3 months preoperatively * Cancer disease * Autoimmune disease incl. rheumatoid arthritis * Pregnant or breast feeding women * Menopause \<1 year

Design outcomes

Primary

MeasureTime frame
Change in concentration of plasma-STAT3 (Signal transducer and activator of transcription) from baseline to 48 hours after surgery48 hours after surgery

Secondary

MeasureTime frame
Change in concentration of plasma-STAT3 from baseline to 14 days after surgery14 days after surgery
Change in concentration of plasma-CREB (Adenosine 3',5'-monophosphate response element-binding protein) from baseline to 14 days after surgery14 days after surgery
Change in concentration of plasma-NF-kB (Nuclear factor kB) from baseline to 14 days after surgery14 days after surgery
Change in Surgical Recovery Scale score from baseline to 28 days after surgery28 days after surgery
Change in modified WOMAC (Western Ontario and McMaster Universities Arthritis Index) score from baseline to 28 days after surgery28 days after surgery

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026