Minimal invasive knee surgery; is it less traumatic? A pilot study

Minimal invasive knee surgery; is it less traumatic? A pilot study - Minimal invasive knee surgery; is it less traumatic?

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON30180

Enrollment

Registered

2006-07-06

Start date

2006-10-30

Completion date

Unknown

Last updated

2024-06-18

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

Conditions

artrosis total knee arthroplasty

Interventions

During the trial blood will be collected from the patients pre and postoperative (2, 4 and 6 hours and day 2 and 4 after surgery)

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - patients receiving a primary total knee arthroplasty - patients with osteoarthritis or avascular necrosis

Exclusion criteria

Exclusion criteria: - pregnancy - clinical relevant disorders, like rheumatoid arthritis, previous knee surgery, standard use of anticoagulantia - unwilling and unable to cooperate in the study

Design outcomes

Primary

Measure	Time frame
Hemoglobin will be determined in terms of blood loss. Blood loss is also measured during the operation and post-operatively in terms of drainporduction. H-FABP tissue damage and IL-6 inflammation reactions Furthermore the patient will be standard evaluated in terms of range of motion, prothesis alignement and pain	—

Secondary

Measure	Time frame
None	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)