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Enrolling by invitation NCT06972914

Effect of Different Wearing Duration of Braces on Short-term Functional Recovery After Anterior Cruciate Ligament Reconstruction

Observational Anterior Cruciate Ligament Reconstruction Rehabilitation

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Anterior Cruciate Ligament Reconstruction Rehabilitation. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

To evaluate the correlation between wearing time of different braces and short-term functional changes such as knee functional score, knee circumference and postoperative recovery Angle after ACL reconstruction, and provide preliminary evidence and key data for subsequent research on whether and how long it is necessary to wear braces after ACL reconstruction.

Primary outcome measures

  • Thigh circumference [Time frame: Preoperative, postoperative 3 weeks, 6 weeks, 3 months, 6 months, 9 months]
  • Degree of Joint range of motion [Time frame: Preoperative, postoperative 3 weeks, 6 weeks, 3 months, 6 months, 9 months]

Eligibility criteria

Inclusion criteria

-Patients with acute anterior cruciate ligament injury undergoing anterior cruciate ligament reconstruction

Exclusion criteria

-Refused to sign the informed consent

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Study design

Observational model
Cohort

Study locations

China · 1 center
  • Peking University Third Hospital of Chongli — Chongli

Identifiers

NCT: NCT06972914 · M2024001

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗