Arthroplasty Complications Clinical Trial
— REVISITSOfficial title:
REVISITS Trial: Revision Single or Two Stage Surgery for Periprosthetic Hip Infection - a Multicentre Randomized Clinical Trial
Hip replacement surgery is common, with over 60,000 cases in Canada annually. After hip
replacement, about 1-2% patients develop a deep infection in their artificial hip implant,
called a periprosthetic joint infection (PJI). It can results in severe pain, disability and
death.
There are two types of surgical treatment: a single-stage revision that involves removing the
joint, thoroughly cleaning the infected area and implanting a new joint, all in the same
surgical procedure; a two-stage revision involves removing the joint, waiting at least 8
weeks while treating the patients with antibiotics and then doing re-implantation of the
joint.
Status | Not yet recruiting |
Enrollment | 110 |
Est. completion date | December 2022 |
Est. primary completion date | September 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Male or female patients aged 18 years or above - A clinical diagnosis of deep hip periprosthetic joint infection according to the Musculoskeletal Infection Society criteria - Require revision surgery (either single-or two-stage revision) for hip periprosthetic joint infection in the opinion of the treating consultant orthopaedic surgeon - The patient is not a candidate for Debridement, Antibiotics and Implant Retention (DAIR) treatment with retention of the implant - Willing and able to sign the written consent, follow the protocol and attend follow-up - Able to read and understand English Exclusion Criteria: - Culture-negative infection (organism not identified) - Patients with systemic sepsis who require emergent surgery - Resistant organisms not sensitive to available intravenous antibiotics - Revision surgery or previous two-stage reimplant - Unable or unwilling to undergo either single-or two-stage revision surgery - Cognitive impairment (dementia, Alzheimer, etc.) which will prevent patients from completing the primary outcome measure - Medical contra-indication to surgery |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
St. Michael's Hospital, Toronto |
Blom AW, Taylor AH, Pattison G, Whitehouse S, Bannister GC. Infection after total hip arthroplasty. The Avon experience. J Bone Joint Surg Br. 2003 Sep;85(7):956-9. — View Citation
Chen SY, Hu CC, Chen CC, Chang YH, Hsieh PH. Two-Stage Revision Arthroplasty for Periprosthetic Hip Infection: Mean Follow-Up of Ten Years. Biomed Res Int. 2015;2015:345475. doi: 10.1155/2015/345475. Epub 2015 Apr 29. — View Citation
Dale H, Fenstad AM, Hallan G, Havelin LI, Furnes O, Overgaard S, Pedersen AB, Kärrholm J, Garellick G, Pulkkinen P, Eskelinen A, Mäkelä K, Engesæter LB. Increasing risk of prosthetic joint infection after total hip arthroplasty. Acta Orthop. 2012 Oct;83(5):449-58. doi: 10.3109/17453674.2012.733918. — View Citation
Kapadia BH, Berg RA, Daley JA, Fritz J, Bhave A, Mont MA. Periprosthetic joint infection. Lancet. 2016 Jan 23;387(10016):386-394. doi: 10.1016/S0140-6736(14)61798-0. Epub 2015 Jun 28. Review. — View Citation
Kunutsor SK, Whitehouse MR, Blom AW, Beswick AD; INFORM Team. Re-Infection Outcomes following One- and Two-Stage Surgical Revision of Infected Hip Prosthesis: A Systematic Review and Meta-Analysis. PLoS One. 2015 Sep 25;10(9):e0139166. doi: 10.1371/journal.pone.0139166. eCollection 2015. Review. — View Citation
Kunutsor SK, Whitehouse MR, Blom AW, Board T, Kay P, Wroblewski BM, Zeller V, Chen SY, Hsieh PH, Masri BA, Herman A, Jenny JY, Schwarzkopf R, Whittaker JP, Burston B, Huang R, Restrepo C, Parvizi J, Rudelli S, Honda E, Uip DE, Bori G, Muñoz-Mahamud E, Darley E, Ribera A, Cañas E, Cabo J, Cordero-Ampuero J, Redó MLS, Strange S, Lenguerrand E, Gooberman-Hill R, Webb J, MacGowan A, Dieppe P, Wilson M, Beswick AD; Global Infection Orthopaedic Management Collaboration. One- and two-stage surgical revision of peri-prosthetic joint infection of the hip: a pooled individual participant data analysis of 44 cohort studies. Eur J Epidemiol. 2018 Oct;33(10):933-946. doi: 10.1007/s10654-018-0377-9. Epub 2018 Apr 5. — View Citation
Kunutsor SK, Whitehouse MR, Lenguerrand E, Blom AW, Beswick AD; INFORM Team. Re-Infection Outcomes Following One- And Two-Stage Surgical Revision of Infected Knee Prosthesis: A Systematic Review and Meta-Analysis. PLoS One. 2016 Mar 11;11(3):e0151537. doi: 10.1371/journal.pone.0151537. eCollection 2016. Review. — View Citation
Lenguerrand E, Whitehouse MR, Beswick AD, Jones SA, Porter ML, Blom AW. Revision for prosthetic joint infection following hip arthroplasty: Evidence from the National Joint Registry. Bone Joint Res. 2017 Jun;6(6):391-398. doi: 10.1302/2046-3758.66.BJR-2017-0003.R1. — View Citation
Lopez D, Leach I, Moore E, Norrish AR. Management of the Infected Total Hip Arthroplasty. Indian J Orthop. 2017 Jul-Aug;51(4):397-404. doi: 10.4103/ortho.IJOrtho_307_16. — View Citation
Phillips JE, Crane TP, Noy M, Elliott TS, Grimer RJ. The incidence of deep prosthetic infections in a specialist orthopaedic hospital: a 15-year prospective survey. J Bone Joint Surg Br. 2006 Jul;88(7):943-8. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Patient-reported hip function | Measured by means of the Oxford Hip Score - A short questionnaire consists of 12 questions ranging from 0 to 48 points, designed to assess function and pain after hip replacement surgery. Higher values represent a better outcome. Scores between 40-48 indicate satisfactory joint function | Questionnaire will be completed by patients at 9 months after surgery | |
Secondary | Health status and quality of life | EuroQol-5D (EQ-5D-5L) is a questionnaire where patients self-rate their level of severity of health status and health-related quality of life. Consists of 5 dimensions (mobility, self care, usual activities, pain/discomfort, anxiety/depression) and each one of them has 5 levels (no problems, slight problems, moderate problems, severe problems, and extreme problems) where patients will indicate how they feel regarding their health status and quality of life. | Questionnaire will be completed by patients before the surgery and at 6, 9, 12 and 24 months after surgery | |
Secondary | Reinfection rates | Recurrence of infection by the same organism or reinfection with a new organism as determined by the criteria using the Musculoskeletal Infection Society criteria. There is a sinus tract communicating with the prosthesis; or A pathogen is isolated by culture from at least two separate tissue or fluid samples obtained from the affected prosthetic joint; or Four of the following six criteria exist: Elevated serum erythrocyte sedimentation rate (ESR) and serum C-reactive protein (CRP) concentration Elevated synovial leukocyte count, Elevated synovial neutrophil percentage (PMN%) Presence of purulence in the affected joint Isolation of a microorganism in one culture of periprosthetic tissue or fluid Greater than five neutrophils per high-power field in five high-power fields observed from histologic analysis of periprosthetic tissue at 400x magnification |
will be assessed at 6 weeks, 3, 6, 9,12 and 24 months after surgery | |
Secondary | Patient-reported hip function | Measured by means of the Oxford Hip Score - A short questionnaire consists of 12 questions ranging from 0 to 48 points, designed to assess function and pain after hip replacement surgery. Higher values represent a better outcome. Scores between 40-48 indicate satisfactory joint function | Questionnaire will be completed by patients at 12 and 24 months after surgery | |
Secondary | Visual Analog Pain Scale | Assess pain from a visual scale that ranges from 0 to 10. Straight line with the endpoints defining extreme limits such as 'no pain at all' (zero) and 'pain as bad as it could be' (ten) | Pain scale will be assessed before the surgery and at 24 and 48 hours, 6 weeks, 3,6, 9, 12 and 24 months after surgery | |
Secondary | Hospital readmission | If patients who were discharged after surgery have an unplanned readmission for any cause to an hospital, the reason for readmission being related or not to the surgery | Will be assessed within 30 days of discharge | |
Secondary | Hospital length of stay | The duration of a single episode of hospitalization (in days) | Will be assessed from admission to discharge (up to 30 days) |
Status | Clinical Trial | Phase | |
---|---|---|---|
Active, not recruiting |
NCT05181566 -
Metal Ion Levels in Total Hip Arthroplasty (THA) With Modular Dual Mobility Cup Compared to Conventional THA
|
N/A | |
Completed |
NCT04490304 -
The Analysis of Posterior Soft Tissue Repair Durability
|
N/A | |
Completed |
NCT05974501 -
Pre vs Post Block in Total Knee Arthroplasty (TKA)
|
Phase 4 | |
Completed |
NCT04565093 -
Efficacy of iPACK After Unilateral TKA
|
N/A | |
Recruiting |
NCT05845021 -
Surgeon-Initiated Bone Health Referral Pathway in Patients Undergoing Lower Extremity Arthroplasty
|
N/A | |
Recruiting |
NCT03306810 -
Recognition and Treatment of Dysglycemia. AGS - Acute Glucose Service
|
N/A | |
Completed |
NCT04289025 -
Modelling and AI Using Sensor Data to Personalise REHABilitation Following Joint Replacement
|
N/A | |
Not yet recruiting |
NCT06469177 -
Patient Centered Post-Op Pain Management Software Tool Interventional Study Verses Standard of Care
|
N/A | |
Not yet recruiting |
NCT05014932 -
Evaluation of Noise Induced by Ceramic-ceramic Friction Torques of Total Hip Prostheses With Customized Femoral Stem
|
||
Active, not recruiting |
NCT04437888 -
Intraoperative Ketamine for Patients Undergoing Total Joint Arthroplasty
|
Early Phase 1 | |
Completed |
NCT05420194 -
Assessment of Postural Stability in Patients With Total Knee Arthroplasty
|
||
Completed |
NCT03269760 -
Multimodal Sleep Pathway for Shoulder Arthroplasty
|
Phase 1 | |
Completed |
NCT03289247 -
Tissue Adhaesive in Wound Closure Following Primary Total Knee Arthroplasty
|
N/A | |
Completed |
NCT04433962 -
Investigation of the Effects of Balance Training on Balance and Functional Status Patients With Total Hip Arthroplasty
|
N/A | |
Recruiting |
NCT06025448 -
Is MIO-RSA Noninferior to BIO-RSA When it Comes to Mechanical Implant Stability?
|
N/A | |
Recruiting |
NCT05459259 -
Physiotherapy for Arthrofibrosis Following Knee Replacement.
|
||
Not yet recruiting |
NCT05736666 -
Treadmill Perturbation Training for Fall Prevention After Total Knee Replacement
|
N/A | |
Active, not recruiting |
NCT03692364 -
Evaluation of Metal-on-conventional-polyethylene vs Ceramic-on-ceramic Articulating Surfaces in Total Hip Arthroplasty
|
N/A | |
Completed |
NCT05013879 -
Kinesiotape for Edema After Bilateral Total Knee Arthroplasty
|
N/A | |
Completed |
NCT04120324 -
Incidence of 30 Day Return to Hospital Following Same Day Discharge Total Hip Arthroplasty
|