Hässleholm Hospital
Hässleholm, Sweden
NCT Number: NCT00436982
The objective is to investigate the Clinical, Radiographic, Roentgen Stereophotogrammetric behaviour and patient outcome when using the Triathlon total knee prosthesis in a prospective randomized clinical trial.
Looking for future studies?
Notify Me18 year–85 year
All sexes
Interventional
Not applicable
Hässleholm, Sweden
The evaluation is carried out by a prospective randomised RSA-study with Triathlon cemented knee prosthesis versus Duracon cemented knee prosthesis.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Orthopaedic implant
Orthopaedic implant
Time frame: 2 years
To compare the maximum total point motion (MTPM) of the Triathlon and Duracon tibial components at two years assessed by means of RSA.
Time frame: 3 months, 1, 5, 7 and 10 years
To compare the maximum total point motion (MTPM) of the Triathlon and Duracon tibial components by means of RSA.
Time frame: [Time Frame: pre-operative, 3 months, 1, 2, 5, 7 and 10 years]
The Knee Society Clinical Rating System is comprised of two distinct sub-scores: one for pain, ROM and joint stability, and one for functional parameters. Sub-scores range from a potential minimum score of 0 to a maximum score of 100 points. Although the specific scores are not distinguished as "excellent," "good," "fair," or "poor," a higher value represents a better outcome.
Time frame: pre-operative, 3 months, 1, 2, 5, 7 and 10 years
KOOS consists of 5 subscales; Pain, other Symptoms, Activities of Daily Living (ADL), Sport and Recreation Function (Sport/Rec) and knee-related Quality of Life (QOL). The previous week is the time period considered when answering the questions. Standardized answer options are given (5 Likert boxes) and each question is assigned a score from 0 to 4. A normalized score (100 indicating no symptoms and 0 indicating extreme symptoms) is calculated for each subscale.
[taken from User Guide] http://www.koos.nu/
Time frame: pre-operative, 3 months, 1, 2, 5, 7 and 10 years
The EQ-5D is a subject-completed questionnaire designed to assess subject health state values. The EQ-5D consists of 2 areas; the EQ visual analogue scale (EQ VAS) and EQ-5D descriptive system. The EQ VAS collects health state values using a 20 cm visual analogue scale with the endpoints labeled best imaginable health state at the top and worst imaginable health state at the bottom, having numeric values of 100 to 0 respectively. The EQ-5D Time Trade-off (TTO) descriptive system comprises the following five dimensions: mobility, self-care, usual activities, pain/comfort and anxiety/depression. Each dimension has three levels: no problems, some problems and extreme problems, where an overall score of 1 represents full health.
NOTE: While the protocol includes pre-operative, 3 months, and 1 year, this data was not collected.
Time frame: intra-operative
Skin to skin operative time
Time frame: preoperative to discharge
Time frame: intra-operative
Blood loss during surgery
Stryker Orthopaedics
Industry
Evaluation of Triathlon - a New Total Knee Prosthesis System. Prospective, Comparative, Randomised, Roentgen Stereophotogrammetric Analysis (RSA) Series
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT04828083
Arthroplasty, Replacement, Knee, Total Knee Arthroplasty
Providence, Rhode Island, United States
View Trial DetailsNCT03965897
Anxiety, Anxiety Disorders
Iowa City, Iowa, United States
View Trial DetailsNCT07231692
Arthroplasty, Replacement, Knee, Neurologic Manifestations
Karabük, Karabük Province, Turkey (Türkiye)
View Trial DetailsNCT07124819
Arthroplasty, Replacement, Hip, Arthroplasty, Replacement, Knee
Bryansk, Russia
View Trial Details