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Synovectomy in Primary Total Knee Arthrplasty

Synovectomy Versus no Synovectomy in Primary Total Knee Arthrplasty : A Randomized Control Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03778463
Enrollment
70
Registered
2018-12-19
Start date
2018-12-31
Completion date
2020-12-31
Last updated
2018-12-19

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

Conditions

Arthroplasty, Replacement, Knee, Synovectomy

Brief summary

The aim of total knee arthroplasty is to achieve best patient functional outcomes, improve patient pain score and satisfaction. Synovial proliferation is a common finding in arthritic knees. Surgeons can't decide if synovectomy is a crucial step in the operation. Studies didn't prove the clear benefits of synovectomy. We are aiming to perform a randomized clinical trial trying to reach the best evidence in that matter.

Interventions

OTHERSynovectomy

Removal of the synovium during total knee arthroplasty

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* patients with primary osteoarthritis undergoing primary total knee arthroplasty

Exclusion criteria

* Inflammatory arthritis * Revision knee arthroplasty

Design outcomes

Primary

MeasureTime frame
Range of motionimmediate postoperative
Functional outcome scores. e.g. knee society score (KSS)one year
knee pain e.g. visual analogue score (VAS) scoreimmediate postoperative
Health related quality of life e.g. short form (SF12) scaleone year
Revision rateone year
Reoperation rateone year

Secondary

MeasureTime frameDescription
Postoperative hemoglobin levelimmediate postoperativegram/dl
Infection ratein first three month
Wound complicationsin first 3 months
Number of patients requiring transfusionimmediate postoperative
Postoperative blood lossimmediate postoperative

Countries

Egypt

Contacts

Primary ContactAhmed Saeed Younis, Dr.
ahmed.s.younis@med.asu.edu.eg201012370677

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026