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Macroscopic and Molecular Changes in Knee Muscular-tendon Unit in Response to Acute Resistant Load

H

Hillel Yaffe Medical Center

Status

Unknown

Conditions

Quadriceps Muscle

Treatments

Diagnostic Test: Ultrasound
Other: Acute resistant load exercises
Behavioral: Background Questionnaire
Diagnostic Test: Percutaneous Needle Core Biopsy
Genetic: DNA and RNA test
Other: Pain Questionnaire

Study type

Interventional

Funder types

Other

Identifiers

NCT03950596
HYMC-58-16

Details and patient eligibility

About

The aim of this study is to determine the influence of acute resistance exercises on anatomical and biological changes in the quadriceps muscle and tendons of the knee

Enrollment

300 estimated patients

Sex

All

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Non-professional athletes
  • Pass heart/lung endurance tests
  • Pass ergometrics testing

Exclusion criteria

  • Have been injured
  • Had physiotherapy for back or lower limbs in past 6 months
  • Orthopedic surgery in lower limbs

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

300 participants in 3 patient groups

One acute resistance load exercise
Active Comparator group
Description:
One hundred volunteers will participate in one acute resistance load exercises to their quadriceps
Treatment:
Diagnostic Test: Ultrasound
Other: Pain Questionnaire
Behavioral: Background Questionnaire
Other: Acute resistant load exercises
Diagnostic Test: Percutaneous Needle Core Biopsy
Genetic: DNA and RNA test
Three acute resistance load exercises
Active Comparator group
Description:
One hundred volunteers will participate in three acute resistance load exercises to their quadriceps
Treatment:
Diagnostic Test: Ultrasound
Other: Pain Questionnaire
Behavioral: Background Questionnaire
Other: Acute resistant load exercises
Diagnostic Test: Percutaneous Needle Core Biopsy
Genetic: DNA and RNA test
Control Group
Active Comparator group
Description:
One hundred volunteers will participate in study as a control group
Treatment:
Diagnostic Test: Ultrasound
Other: Pain Questionnaire
Behavioral: Background Questionnaire
Diagnostic Test: Percutaneous Needle Core Biopsy
Genetic: DNA and RNA test

Trial contacts and locations

1

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Central trial contact

Eias Kassem, MD

Data sourced from clinicaltrials.gov

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