anterior cruciate ligament tear.
Conditions
Interventions
Intervention 1: Intervention group: First: 21 patients undergo anterior cruciate ligament surgery with patellar tendon. Intervention 2: Intervention group: The second group: 21 patients undergo hamstr
Sponsors
Artesh University of Medical Sciences
Eligibility
Sex/Gender
Male
Inclusion criteria
Inclusion criteria: 1. Patients who undergo anterior cruciate ligament resection surgery 2. Over 18 years of age 3. BMI = 35 Willingness and ability to prepare a written consent form 4. Willingness and ability to perform subjective evaluations and have the ability to understand written questionnaires 5, Suffering from rupture 6. Present May he not take any medicine that changes knee symptoms throughout the study until the end. 7. Willingness and ability to agree to the conditions related to the study and procedures and visits.
Exclusion criteria
Exclusion criteria: 1. Injuries associated with ACL such as torn meniscus or posterior cruciate ligament 2. Follow-up of patients under 12 months 3, Patients who had complications such as thrombosis or embolism during or immediately after surgery 4, Patients who do not come for follow-up 5, Diseases High-risk medical condition such as kidney, liver and heart failure 6, History of addiction 7, A history of any surgery related to the knee 8. Contraindications for imaging and MRI 9. Mental disorders 10. Progressive neurological disorders 11. Having pain in another place that causes disturbance in the assessment of shoulder pain
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Army employees and soldiers who have ruptured the anterior cruciate ligament, their demographic information is obtained by interviewing and completing a questionnaire, then after randomization, random allocation, and concealment, they are randomly divided into 3 groups, and each group undergoes a type of surgery by They are placed by a surgeon and with a fixation method, and immediately after the operation, as well as the follow-up periods of 3, 6, and 12 months, they are examined and asked about function (Lee Scholem questionnaire), pain level, and clinical examinations of ligament laxity, and at the end, the patient information is provided by the program. SPSS is subjected to statistical analysis. Timepoint: Immediately after the operation, as well as the follow-up periods of 3, 6, and 12 months. Method of measurement: They are examined and questioned in terms of function (Lee Scholem questionnaire), pain level and clinical examinations for ligament laxity. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactNima hoseinizare
Artesh University of Medical Sciences
Outcome results
None listed