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Knee Exam

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121. A Prospective Radiostereometric Analysis (RSA) and Clinical Evaluation of the Triathlon Tritanium Total Knee Replacement

Tritanium components. The investigators expect to see a correlation between radiolucent lines and migration characteristics using RSA. The investigators expect that inducible displacement exams taken at 2 years post-operative will be able to distinguish between patients identified by RSA measurements as having inadequate fixation. The investigators expect to see a significant difference in health status and functional outcomes before and after total knee replacement using the Triathlon Tritanium knee (...) A Prospective Radiostereometric Analysis (RSA) and Clinical Evaluation of the Triathlon Tritanium Total Knee Replacement A Prospective Radiostereometric Analysis (RSA) and Clinical Evaluation of the Triathlon Tritanium Total Knee Replacement - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum

2015 Clinical Trials

122. Diagnosis and classification of chondral knee injuries: comparison between magnetic resonance imaging and arthroscopy. (PubMed)

Diagnosis and classification of chondral knee injuries: comparison between magnetic resonance imaging and arthroscopy. To compare the magnetic resonance imaging (MRI) findings of patients undergoing knee arthroscopy for chondral lesions. The hypothesis was that MRI displays low sensitivity in the diagnosis and classification of chondral injuries.A total of 83 knees were evaluated. The MRIs were performed using the same machine (GE SIGNA HDX 1.45 T). The MRI results were compared (...) with the arthroscopy findings, and an agreement analysis was performed. Thirty-eight of the 83 MRI exams were evaluated by another radiologist for inter-observer agreement analysis. These analyses were performed using the kappa (κ) coefficient.The highest incidence of chondral injury was in the patella (14.4 %). The κ coefficient was 0.31 for the patellar surface; 0.38 for the trochlea; 0.46 for the medial femoral condyle; 0.51 for the lateral femoral condyle; and 0.19 for the lateral plateau. After dividing

2015 Knee Surgery, Sports Traumatology, Arthroscopy

123. Repeat Injection of Cingal® for Osteoarthritis of the Knee

Repeat Injection of Cingal® for Osteoarthritis of the Knee Repeat Injection of Cingal® for Osteoarthritis of the Knee - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Repeat Injection of Cingal® (...) for Osteoarthritis of the Knee The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT02381652 Recruitment Status : Completed First Posted : March 6, 2015 Last Update Posted : June 22, 2015 Sponsor: Anika Therapeutics, Inc. Information provided by (Responsible Party): Anika Therapeutics, Inc. Study Details Study

2015 Clinical Trials

124. Validation of quantitative magnetic resonance imaging-based apparent bone volume fraction in peri-articular tibial bone of cadaveric knees. (PubMed)

Validation of quantitative magnetic resonance imaging-based apparent bone volume fraction in peri-articular tibial bone of cadaveric knees. In the knee, high-resolution magnetic resonance (MR) imaging has demonstrated that increased apparent bone volume fraction (trabecular bone volume per total volume; BV/TV) in the peri-articular proximal medial tibia is associated with joint space narrowing and the presence of bone marrow lesions. However, despite evidence of construct validity, MR-based (...) apparent BV/TV has not yet been cross-validated in the proximal medial tibia by comparison with a gold standard (e.g., micro-computed tomography [microCT]). In this cadaveric validation study we explored the association between MR-based apparent BV/TV and microCT-based BV/TV in the proximal peri-articular medial tibia.Fresh cadaveric whole knee specimens were obtained from individuals 51 to 80 years of age with no knee pathology other than osteoarthritis. Ten knees were collected from five cadavers

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2014 BMC Musculoskeletal Disorders

125. Bariatric Lap Band Surgery as a Treatment for Knee Osteoarthritis

)37. It is the application of this approved procedure that constitutes the research question should LAGB surgery be considered as a treatment option to improve pain and physical disability in patients with knee OA? During the pre-operative process patients will be given study questionnaires to evaluate knee pain and function, have a musculoskeletal exam and blood/urine will be collected.These procedures will be repeated at post-operative intervals to track response of the knees to the LAGB (...) Bariatric Lap Band Surgery as a Treatment for Knee Osteoarthritis Bariatric Lap Band Surgery as a Treatment for Knee Osteoarthritis - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Bariatric Lap Band Surgery

2014 Clinical Trials

126. An Open-label, Single Arm, Multi-center, Phase 3 Study to Evaluate the Safety and Efficacy of Retreatment With Intra-articular LBSA0103 Injections in the Patients With Osteoarthritis of the Knee

An Open-label, Single Arm, Multi-center, Phase 3 Study to Evaluate the Safety and Efficacy of Retreatment With Intra-articular LBSA0103 Injections in the Patients With Osteoarthritis of the Knee A Clinical Trial to Evaluate the Safety and Efficacy of Retreatment With Intra-articular LBSA0103 Injections in the Patients With Osteoarthritis of the Knee - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information (...) . Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. A Clinical Trial to Evaluate the Safety and Efficacy of Retreatment With Intra-articular LBSA0103 Injections in the Patients With Osteoarthritis of the Knee The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been

2014 Clinical Trials

127. Phase 1, Dose Escalation Study Evaluating the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of SM04690 in Moderate to Severe Knee Osteoarthritis (OA)

for this study will include adverse events, dose limiting toxicity (DLT), physical exams, vital signs, ECGs, and clinical laboratory tests [ Time Frame: during 24 weeks ] Additional safety assessment of bone loss as measured by CT of the knee [ Time Frame: during 24 weeks ] The following PK parameters will be determined from the plasma of SM04690; Cmax, Tmax, AUC0-t, AUC0-∞, and t1/2 [ Time Frame: during 12 weeks ] Secondary Outcome Measures : Change from baseline pain over the last 48 hours using a Visual (...) Phase 1, Dose Escalation Study Evaluating the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of SM04690 in Moderate to Severe Knee Osteoarthritis (OA) Phase 1, Dose Escalation Study Evaluating the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of SM04690 in Moderate to Severe Knee Osteoarthritis (OA) - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x

2014 Clinical Trials

128. Study of Suture Repair of Torn Meniscus in the Knee

Study of Suture Repair of Torn Meniscus in the Knee Study of Suture Repair of Torn Meniscus in the Knee - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Study of Suture Repair of Torn Meniscus in the Knee (...) Study Description Go to Brief Summary: Horizontal meniscus tears meeting specified criteria will be repaired by any commonly used suture technique. Subjects will be followed for 2 years to evaluate the effectiveness of the repair, by assessing the re-operation rate, and by assessing improvements in knee pain and knee function. Condition or disease Intervention/treatment Phase Meniscal Tear Meniscus Tear Device: Suture-based meniscal repair Not Applicable Detailed Description: Potential subjects

2014 Clinical Trials

129. Tack Optimized Balloon Angioplasty Below the Knee (TOBA

Tack Optimized Balloon Angioplasty Below the Knee (TOBA Tack Optimized Balloon Angioplasty Below the Knee (TOBA - BTK) Study - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Tack Optimized Balloon (...) Angioplasty Below the Knee (TOBA - BTK) Study (TOBABTK) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT02235675 Recruitment Status : Completed First Posted : September 10, 2014 Last Update Posted : March 8, 2017 Sponsor: Intact Vascular Information provided by (Responsible Party): Intact Vascular Study

2014 Clinical Trials

130. Effectiveness of Aquatic Physical Therapy for Knee Osteoarthritis Patients

Effectiveness of Aquatic Physical Therapy for Knee Osteoarthritis Patients Effectiveness of Aquatic Physical Therapy for Knee Osteoarthritis Patients - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more (...) . Effectiveness of Aquatic Physical Therapy for Knee Osteoarthritis Patients (RCT-OA) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT02247882 Recruitment Status : Completed First Posted : September 25, 2014 Last Update Posted : May 25, 2017 Sponsor: Universidade Estadual de Londrina Collaborators: Ministry

2014 Clinical Trials

131. Pilot Study of PEMF Therapy in Treatment of Post-operative Pain Following Total Knee Arthroplasty

investigational drug or device within 30 days prior to the Screening Visit or is enrolled in another clinical trial. Subjects consuming an average of > 100 mg oral Morphine Sulfate equivalents per day during the run-in phase. Subject has evidence on physical or radiological exam of joint instability or infection involving the index knee. Passive range of motion demonstrates maximal flexion of the index knee < 90 degrees or maximal extension of the index knee < -10 degrees. Body Mass Index (BMI) < 19 kg/m2 (...) Pilot Study of PEMF Therapy in Treatment of Post-operative Pain Following Total Knee Arthroplasty Pilot Study of PEMF Therapy in Treatment of Post-operative Pain Following Total Knee Arthroplasty - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove

2014 Clinical Trials

132. Persona Total Knee Arthroplasty Outcomes Study

the contacts provided below. For general information, Layout table for eligibility information Ages Eligible for Study: 18 Years to 75 Years (Adult, Older Adult) Sexes Eligible for Study: All Accepts Healthy Volunteers: No Criteria Inclusion Criteria: Patient 18-75 years of age, inclusive Patient qualifies for primary total knee arthroplasty based on physical exam and medical history, including diagnosis of severe knee pain and disability due to at least one of the following: a) rheumatoid arthritis (...) Persona Total Knee Arthroplasty Outcomes Study Persona Total Knee Arthroplasty Outcomes Study - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Persona Total Knee Arthroplasty Outcomes Study The safety

2014 Clinical Trials

133. Non-Ablative Fractional Resurfacing of Total Knee Replacement Scars

groups. Additionally, any data collected at routine follow-ups will be collected and analyzed. This includes baseline demographic information as well as physical exam findings, including pre-operative and post-operative knee range of motion (ROM). The KOOS adopted the Western Ontario and McMaster Universities Arthritis Index and added two additional subscales to evaluate knee function after ligament, articular cartilage, or meniscal injury, and their respective treatments. The KOOS proved (...) Non-Ablative Fractional Resurfacing of Total Knee Replacement Scars Non-Ablative Fractional Resurfacing of Total Knee Replacement Scars - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Non-Ablative

2014 Clinical Trials

134. Outcome Study of Highly-cross Linked Polyethylene vs. Standard Polyethylene for Primary Posterior Stabilized (PS) Total Knee

or disease Intervention/treatment Arthroplasty, Replacement, Knee Device: knee arthroplasty, standard polyethylene Device: knee arthroplasty, XLP polyethylene Detailed Description: This prospective, randomized study will seek to enroll patients undergoing primary total knee arthroplasty. Preoperative evaluation will include a detailed history and physical exam with clinical data collection (SF-36, WOMAC, and Knee Society Scores), a complete description of the procedure, a demonstration of the actual (...) Outcome Study of Highly-cross Linked Polyethylene vs. Standard Polyethylene for Primary Posterior Stabilized (PS) Total Knee Outcome Study of Highly-cross Linked Polyethylene vs. Standard Polyethylene for Primary Posterior Stabilized (PS) Total Knee - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached

2014 Clinical Trials

135. Study to Evaluate Safety/Efficacy of a Single Pre-Op Dose of AYX1 Injection to Treat Pain After Knee Replacement Surgery

Study to Evaluate Safety/Efficacy of a Single Pre-Op Dose of AYX1 Injection to Treat Pain After Knee Replacement Surgery Study to Evaluate Safety/Efficacy of a Single Pre-Op Dose of AYX1 Injection to Treat Pain After Knee Replacement Surgery - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum (...) number of saved studies (100). Please remove one or more studies before adding more. Study to Evaluate Safety/Efficacy of a Single Pre-Op Dose of AYX1 Injection to Treat Pain After Knee Replacement Surgery The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT02081703 Recruitment Status : Completed First

2014 Clinical Trials

136. Knee, Anterior Cruciate Ligament Injuries (MRI)

Knee, Anterior Cruciate Ligament Injuries (MRI) MRI for Anterior Cruciate Ligament Injury: Overview, Anatomy, Mechanism of Injury Edition: No Results No Results Please confirm that you would like to log out of Medscape. If you log out, you will be required to enter your username and password the next time you visit. https://profreg.medscape.com/px/getpracticeprofile.do?method=getProfessionalProfile&urlCache=aHR0cHM6Ly9lbWVkaWNpbmUubWVkc2NhcGUuY29tL2FydGljbGUvNDAwNTQ3LW92ZXJ2aWV3 processing (...) > MRI for Anterior Cruciate Ligament Injury Updated: Jan 24, 2016 Author: Anton M Allen, MD; Chief Editor: Felix S Chew, MD, MBA, MEd Share Email Print Feedback Close Sections Sections MRI for Anterior Cruciate Ligament Injury Overview Overview The (ACL) is the most commonly injured of the major knee ligaments. These injuries plague both athletes and nonathletes. The ACL is a vital ligamentous stabilizer of the knee that resists anterior translation and secondarily resists varus and valgus forces

2014 eMedicine Radiology

137. Clinical examination of the knee: know your tools for diagnosis of knee injuries (PubMed)

Clinical examination of the knee: know your tools for diagnosis of knee injuries The clinical evaluation of the knee is a fundamental tool to correctly address diagnosis and treatment, and should never be replaced by the findings retrieved by the imaging studies carried on the patient.Every surgeon has his own series of exams with whom he is more confident and on whom he relies on for diagnosis. Usually, three sets of series are used: one for patello-femoral/extensor mechanism pathologies; one (...) for meniscal and chondral (articular) lesions; and one for instability evaluation.This review analyses the most commonly used tests and signs for knee examination, outlining the correct way to perform the test, the correct interpretation of a positive test and the best management for evaluating an injured knee both in the acute and delayed timing.

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2011 Sports Medicine, Arthroscopy, Rehabilitation, Therapy & Technology: SMARTT

138. Ultrasound Findings of Finger, Wrist and Knee Joints in Mucopolysaccharidosis

: Power Doppler [ Time Frame: one time exam ] The primary objective is to determine whether patients with various types of MPS and at various stages of the disease exhibit abnormalities of the finger, wrist and knee joints as assessed by grey scale and Power Doppler ultrasonography. Secondary Outcome Measures : Ultrasound scanning technique [ Time Frame: one time scan ] To determine the optimal ultrasound scanning technique for MPS patients given the potentially advanced joint contractures Findings (...) Ultrasound Findings of Finger, Wrist and Knee Joints in Mucopolysaccharidosis Ultrasound Findings of Finger, Wrist and Knee Joints in Mucopolysaccharidosis - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more

2013 Clinical Trials

139. Amniotic Membrane in Total Knee Replacements to Reduce Scarring

staff using the contacts provided below. For general information, Layout table for eligibility information Ages Eligible for Study: 18 Years and older (Adult, Older Adult) Sexes Eligible for Study: All Accepts Healthy Volunteers: No Criteria Inclusion Criteria: Are adults ages 18 or older. Are diagnosed with advanced osteoarthritis as determined by clinical exam and necessitate total knee replacement. Have a willingness to comply with follow-up examination. Have ability to give full written consent (...) Amniotic Membrane in Total Knee Replacements to Reduce Scarring Amniotic Membrane in Total Knee Replacements to Reduce Scarring - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Amniotic Membrane in Total

2013 Clinical Trials

140. Feasibility Trial Using Imaging and Biochemical Technologies to Measure Knee Cartilage Composition in Acute ACL Injury

requiring surgical intervention Have cartilage resurfacing procedures performed at the time of injury Inability to undergo the standard pre- and post-injury/operative rehabilitation Varus or valgus instability requiring ligament repair or reconstruction (from clinical exam at time of injury) History of osteoarthritis and inflammatory arthritis Women who are pregnant are excluded Previous injury and/or surgery on either knee Contacts and Locations Go to Information from the National Library of Medicine (...) Feasibility Trial Using Imaging and Biochemical Technologies to Measure Knee Cartilage Composition in Acute ACL Injury Feasibility Trial Using Imaging and Biochemical Technologies to Measure Knee Cartilage Composition in Acute ACL Injury - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum

2013 Clinical Trials

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