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Evaluating Knee Function and Recovery in Patients After Anterior Cruciate LigamentL Reconstruction

Functional Analysis of Patients Undergoing Anterior Cruciate Ligament Reconstruction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-2ttqd58
Enrollment
18
Registered
2026-04-14
Start date
2022-01-01
Completion date
Unknown
Last updated
2026-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anterior Cruciate Ligament Injuries

Interventions

This study is a randomized controlled trial. Participants were randomly assigned to one of two study arms using a computer-generated randomization sequence. Regarding blinding, the study was double-bl

Sponsors

Universidade Federal de Juiz de Fora
Lead Sponsor
Universidade Federal de Juiz de Fora
Collaborator

Eligibility

Age
16 Years to 40 Years

Inclusion criteria

Inclusion criteria: Age between 16 and 40 years; both sexes; patients from the Knee Surgery outpatient clinic at Hospital Universitário da Universidade Federal de Juiz de Fora; indication for elective knee surgeries (ligament or meniscal repair).

Exclusion criteria

Exclusion criteria: Presence of concomitant pathologies (previous muscle alterations, morbid obesity, or autoimmune diseases); cardiovascular or metabolic diseases; smoking; use of illicit drugs or anabolic steroids; use of supplements that accelerate metabolism or affect vascular dilation; indication for total or partial knee arthroplasty.

Design outcomes

Primary

MeasureTime frame
It’s expected to observe: Assessment of postoperative pain; evaluation of edema; range of motion (ROM) in early recovery

Secondary

MeasureTime frame
Analysis of muscle tissue damage caused by the tourniquet; assessment of cellular and tissue-level integrity using optical and electron microscopy

Countries

BR

Contacts

Public ContactBruno do Nascimento

Universidade Federal de Juiz de Fora

bruno_fajardo@yahoo.com.br+55-32-99997-2112

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: May 1, 2026