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Comparison of two different approaches to knee replacement surgery

Knee Incision Trial: a randomised controlled trial to compare wound ooze after midline vs curved medial para-patellar skin incisions in knee replacement

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN13723185
Enrollment
60
Registered
2020-03-16
Start date
2020-03-02
Completion date
Unknown
Last updated
2023-05-08

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

Conditions

Conditions requiring knee replacement Musculoskeletal Diseases Conditions requiring knee replacement

Interventions

All patients recruited to the study will have a routine Total Knee Replacement as they would normally on the NHS in Weston General Hospital. On admission they will be randomised into one of the two st

Sponsors

Weston Area Health NHS Trust
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 18 years or older 2. Undergoing planned primary Total Knee Replacement surgery in Weston General Hospital

Exclusion criteria

Exclusion criteria: 1. Patients for revision procedures 2. Previous open procedures on the knee 3. Bleeding disorders or medical conditions/complications requiring therapeutic anticoagulation (eg DVT, PE, MI), even if these complications occur post-operatively 4. History of previous trauma to the knee 5. Known allergy to skin adhesives 6. Deviation from post-operative protocol 7. Significant medical condition which has an effect on wound healing (eg diabetes or rheumatological disease) 8. Obesity

Design outcomes

Primary

MeasureTime frame
Wound ooze on day 1 to day 4, using graph paper printed onto acetate sheets which can by laid onto the dressing, allowing the size of dressing marking to be measured by counting the number of squares on the graph paper which are involved

Secondary

MeasureTime frame
1. The length of inpatient stay (days) following the surgery 2. Whether or not an expensive 'PICO' dressing is required (only if the patient has persistent wound ooze more than 2x2cm at day 4) 3. Patient satisfaction with the appearance and function of the scar as assessed by means of a validated wound scoring system, the Patient and Observer Scar Assessment Scale (POSAS) (the patient assessment part of this questionnaire) at week 4 and week 6 post-operatively

Countries

England, United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026