Trial · NCT07107581
Exactech Knee Systems Post Market Clinical Follow-up
NCT07107581, Enrolling by invitation, Exactech
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Exactech Knee Systems Post Market Clinical Follow-up. Trials, record NCT07107581. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07107581
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Exactech Knee Systems Post Market Clinical Follow-up
- NCT number
- NCT07107581
- Status
- Enrolling by invitation
- Enrollment
- 1,879 participants, estimated
- Lead sponsor
- Exactech
- Conditions
- Knee Arthroplasty, Total, Partial Knee Replacement
- Interventions
- Prospective / Subjects Knee Arthroplasty, Retrospective to Prospective, Retrospective Only Subjects
- First posted
- 2025-08-06
- Last updated
- 2025-08-06
Source ClinicalTrials.gov
Registered outcomes2
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Primary Objective | 10 Years | The objective of this study is to assess the safety and performance of Exactech Knee System devices. Data will be collected to provide objective evidence of safety and performance of Exactech Knee Systems used in primary knee arthroplasty. Data may be analyzed to support future presentations and publications of an Exactech Knee System and may be used to provide clinical evidence of the post market outcomes of Exactech Knee Systems to regulatory authorities when required. The following data will be collected: Demographics (e.g., height, weight, age, and gender), Preoperative information (e.g., indication for surgery, comorbidities, pre-surgical assessments of knee function), Operative details (e.g., intra-operative findings, surgical approach, length of surgery), Product information (components used in the knee surgery), Adverse events (e.g., infection, device failure, revision), Implant survivorship, \& Patient Reported Outcomes (KOOS, KSS, HSS, OKS and/or VAS) |
| Secondary | Secondary Objective | 10 Years | Collect radiographic data when available to examine radiographic outcomes. Analyze safety and performance of Exactech Knee System components when used in revision cases. Appropriate radiographs should be obtained to allow proper evaluation of the knee(s) by the investigator. The evaluation of the radiographs should be documented on the appropriate case report form for each applicable visit. 1. Radiographic views include: 1. AP View (weight bearing) 2. Lateral View 3. Patellar Skyline or Merchant View 2. Radiographic evaluations include: 1. Preoperative visit 2. Immediate postoperative visit 3. Post-operative follow-up visits 3. Radiographic assessments include: 1. Knee alignment 2. Patellofemoral evaluation 3. Radiolucent lines 4. Subsidence |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers3
The papers the trial lists on ClinicalTrials.gov.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07107581
GET https://conductscience.org/api/trials/v1/NCT07107581/registered