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Trial · NCT07886463

Functional Biomechanical Analysis in Patients Who Underwent Lateral Ankle Ligament Repair With Augmentation

NCT07886463, Not applicable, Recruiting, Clinique du Sport, Bordeaux Mérignac

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Functional Biomechanical Analysis in Patients Who Underwent Lateral Ankle Ligament Repair With Augmentation. Trials, record NCT07886463. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07886463

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Functional Biomechanical Analysis in Patients Who Underwent Lateral Ankle Ligament Repair With Augmentation
NCT number
NCT07886463
Status
Recruiting
Phases
Not applicable
Enrollment
39 participants, estimated
Lead sponsor
Clinique du Sport, Bordeaux Mérignac
Conditions
Chronic Lateral Ankle Instability
Interventions
Biomechanical motion analysis
First posted
2026-10-21
Last updated
2026-10-21

Source ClinicalTrials.gov

Registered outcomes10

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryChange in biomechanical parameters derived from three-dimensional motion analysisFrom enrollement to 6 months after surgery
Change in Kinematic parameters derived from three-dimensional motion analysis between the preoperative assessment (T0), the 3-month postoperative assessment (T1), and the 6-month postoperative assessment (T2). Kinematic variables include ankle, knee, hip, trunk, and pelvic joint angles (°). Data will be collected using a 12-camera Qualisys MIQUS M3 optoelectronic motion capture system (Qualisys AB, Gothenburg, Sweden).
SecondaryChanges in Kinetic Moments MeasurementsFrom enrollement to 6 months after surgeryKinetic and inverse dynamics measures at T0, T1, and T2 include : * Ankle, knee, and hip extensor joint moments (N·m/kg) * Knee adduction moment (N·m/kg)
SecondaryChanges in Spatiotemporal ParametersFrom enrollement to 6 months after surgerySpatiotemporal parameters measured at T0, T1, and T2 include: * Ground contact time (s) * Stance phase duration (s) * Flight phase duration (s)
SecondaryLimb Symmetry Index (LSI) for selected biomechanical parametersFrom enrollement to 6 months after surgery
Inter-limb symmetry will be expressed as a Limb Symmetry Index (LSI), calculated as: LSI = (Operated limb value / Contralateral limb value) × 100 Values will be expressed as percentages (%). Separate analyses will be performed for each predefined biomechanical parameter.
SecondaryChange in Limb Symmetry Index over timeFrom inclusion to 6 months post-surgeryEvolution of the Limb Symmetry Index (LSI) between baseline (T0), 3 months (T1), and 6 months (T2) following surgery.
SecondaryCountermovement Jump (CMJ) HeightFrom Inclusion to 6 months post-surgeryVertical jump height measured during the Countermovement Jump (CMJ), expressed in centimeters.
SecondaryDrop Jump HeightFrom enrollement to 6 months after surgeryVertical jump height measured during the Drop Jump task, expressed in centimeters.
SecondaryChanges in Kinetic Joint Power MeasurementsFrom enrollement to 6 months after surgeryKinetic and inverse dynamics measures at T0, T1, and T2 include : Positive and negative joint power at the knee and ankle (W/kg)
SecondaryChanges in Kinetic Vertical ground reaction force MeasurementsFrom enrollement to 6 months after surgeryKinetic and inverse dynamics measures at T0, T1, and T2 include : Vertical ground reaction force (vGRF) (N)
SecondaryChanges in Kinetic Reaction Forces MeasurementsFrom enrollement to 6 months after surgeryKinetic and inverse dynamics measures at T0, T1, and T2 include : Anterior-posterior braking and propulsive ground reaction forces (N/kg)

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.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

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.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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/NCT07886463

GET https://conductscience.org/api/trials/v1/NCT07886463/registered