ClinicalTrials.Veeva

Menu

The Influence of Running to ACL Deficiency

G

Guangzhou General Hospital of Guangzhou Military Command

Status

Completed

Conditions

ACL Injury
Gait

Treatments

Procedure: Procedure

Study type

Interventional

Funder types

Other

Identifiers

NCT03135600
GuangzhouGH008

Details and patient eligibility

About

The aim of this study is to investigate the influence of running to kinematic parameters of patients with anterior cruciate ligament.

Enrollment

60 patients

Sex

All

Ages

20 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. 20< age < 30.
  2. Body mass index < 30.
  3. For controls, no history of major injury or surgery in lower limbs; no symptoms of lower limbs; physical examination to test the lower limbs to be healthy.
  4. For ACLD group, history of knee injury for at least 2 weeks and able to walk and run; confirmed to be unilateral ACL injury by MRI; knee pain in the knee (ACL injury).
  5. The habit of moderate exercise (e.g. Jogging) at least once a week for at least 30 minutes.

Exclusion criteria

  1. Body mass index >30.
  2. For controls, injury or surgery in hip/knee/ankle.
  3. For ACLD group, injury or surgery in hip/ankle; confirmed to be no ACL injury by arthroscopy.
  4. Neuropathic disease.
  5. Muscular disease.
  6. Lack ability to finish the procedure physically or mentally.
  7. Easy to fall.
  8. Any other conditions that can influence gait parameters of the lower limbs.

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Single Blind

60 participants in 2 patient groups

Normal
Experimental group
Description:
The participants from this group are healthy people.
Treatment:
Procedure: Procedure
ACLD
Experimental group
Description:
The participants from this group suffer from anterior cruciate ligament injury.
Treatment:
Procedure: Procedure

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems