Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02050438
Other study ID # COTCSPT1JV
Secondary ID
Status Completed
Phase N/A
First received January 29, 2014
Last updated July 25, 2014
Start date January 2014

Study information

Verified date July 2014
Source Corporacion Parc Tauli
Contact n/a
Is FDA regulated No
Health authority Spain: Departament de Salut de la Generalitat de Catalunya
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine whether different kind of prostesis designs influences in the quality of life of patients


Description:

Objectiu Criteris d'inclusiĆ³ Mesura dels resultats


Recruitment information / eligibility

Status Completed
Enrollment 135
Est. completion date
Est. primary completion date July 2014
Accepts healthy volunteers No
Gender Both
Age group 65 Years to 80 Years
Eligibility Inclusion Criteria:

- Aged 65-80 years.

- Primary Ostheortritis

- Mechanical Axis 0+/- 7 degrees

Exclusion Criteria:

- Patients with any new important disease after the surgical procedure.

- Important complications related with the surgical procedure, as fractures, infections and vascular lesions.

- Patients not following a rehabilitation program

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Intervention

Procedure:
Total Knee Arthroplasty


Locations

Country Name City State
Spain Corporació Sanitària Parc Taulí Sabadell Barcelona

Sponsors (1)

Lead Sponsor Collaborator
Corporacion Parc Tauli

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Quality of Life 6 months No
Secondary Functional Results 6 months No
See also
  Status Clinical Trial Phase
Terminated NCT04040985 - Legion Primary Safety and Efficacy N/A
Recruiting NCT05279092 - Yale Steroid Enhanced Versus Exparel Nerveblock TKA RCT Study Phase 2
Completed NCT03286543 - Electrical Stimulation for the Treatment of Pain Following Total Knee Arthroplasty Using the SPRINT Beta System N/A
Not yet recruiting NCT04594447 - Physica System KR vs Physica System CR (K-20) N/A
Completed NCT02413996 - Effects of Virtual Reality Rehabilitation in Patients With Total Knee Arthroplasty N/A
Completed NCT01500252 - Patellar Resurfacing Versus Patellar Retention in Total Knee Arthroplasty - A Randomized Clinical Trial Phase 4
Completed NCT04081493 - The Efficacy of Low-load Blood Flow Restricted Resistance Before TKR N/A
Active, not recruiting NCT03339557 - Comparison of Three Knee Replacements N/A
Enrolling by invitation NCT04513145 - Adductor Canal Block Phase 2/Phase 3
Completed NCT06045078 - Aromatherapy in Total Knee Replacement N/A
Completed NCT02468934 - Electrical Stimulation for the Treatment of Pain Following Total Knee Arthroplasty (TKA) Using the SPRINT System N/A
Completed NCT02914210 - Virtual vs. Traditional Physical Therapy Following Total Knee Replacement N/A
Withdrawn NCT01523418 - Study to Observe Safety of Xarelto in VTE Prophlylaxis After Elective TKR (Total Knee Replacement) or THR (Total Hip Replacement) N/A
Completed NCT00795223 - Comparative Pain Control Between 0.2 or 0.3 Spinal Morphine and 0.25 or 0.5 % Bupivacaine for FNB After TKA Phase 4
Completed NCT01307202 - Morphine Consumption in Joint Replacement Patients, With or Without Gabapentin Treatment N/A
Completed NCT01522781 - 10 Year Outcome of Total Knee Replacement (TKR) Using Sigma Prosthesis N/A
Completed NCT01515449 - Predictors of Poor Outcomes in 1038 Sigma Knees N/A
Completed NCT04166539 - Neurotoxicity and Cardiotoxicity in Total Joint Arthroplasty
Completed NCT03454256 - Virtual Reality Rehabilitation in Patients With Total Knee Replacement N/A
Enrolling by invitation NCT06118073 - Effect of Mindfulness on Pain After Total Knee Arthroplasty N/A