Trials / Completed
CompletedNCT01355900
Comparison of Three Tourniquet Application Methods in Primary Total Knee Arthroplasty Surgery
Influence of the Intraoperative Tourniquet Application Method on the Perioperative Blood Loss, Frequency of Transfusion and Close Postoperative Outcomes in Primary Total Knee Arthroplasty Patients
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 120 (actual)
- Sponsor
- Vilnius University · Academic / Other
- Sex
- All
- Age
- 50 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
Different strategies of tourniquet application during elective primary total knee arthroplasty are thought to be associated with different outcomes. In that context, the study investigates different tactics in the search of optimal application of the tourniquet and the related fluid management during 24 perioperative hours.
Detailed description
The optimal application of tourniquet should reduce perioperative blood loss, create bloodless operative field, improve cementing technique and shorten surgery time. Meanwhile, inadequate application may increase the risk of deep vein thrombosis and pulmonary thromboembolism. Previous attempts to compare the tourniquet strategies in respect to the perioperative blood loss did not show significant difference. The investigators use the volume loading test aiming to optimize the fluid status and obtain the hemoglobin concentration in the conditions of standardized plasma dilution. The test is deployed just before the surgery and after postoperative 24 hrs in ICU. Functional outcomes and possible length of hospital stay is also evaluated.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Total knee arthroplasty performed under tourniquet | Comparison of the different tourniquet tactics. |
Timeline
- Start date
- 2010-01-01
- Primary completion
- 2014-01-01
- Completion
- 2014-01-01
- First posted
- 2011-05-18
- Last updated
- 2014-03-04
Locations
1 site across 1 country: Lithuania
Source: ClinicalTrials.gov record NCT01355900. Inclusion in this directory is not an endorsement.