Comparison of the Functional Outcome of Site Peroneus Longus Graft Donors With and Without Distal Stump Suturing of Peroneus Tendon Brevis on ACL Reconstruction Case in Cipto Mangunkusumo Hospital in Jakarta With 24 Patient as Subject Who Will Divide Into 2 Group.
1 other identifier
interventional
24
1 country
1
Brief Summary
Injury of the Anterior Cruciate Ligament (ACL) is one of the most common sports injuries. The incidence rate reaches 68.6 cases per 100,000 people per year. Management of ACL injuries for individuals who want to return to the level of exercise activity as before, mostly in the form of reconstructive surgery. As many as 60,000 to 175,000 cases of ACL reconstruction per year are carried out in the United States At present, many reconstructive surgeries are performed by taking tendon grafts on the patient's own body (autograft) to then be used instead of the ACL. The most widely used graft sources are Hamstring and Bone-Patellar Tendon-Bone (BPTB) grafts. Other alternative grafts are Quadriceps tendon, Fascia Lata, Iliotibial Band, and Peroneus Longus Tendon. Each graft retrieval technique has advantages and disadvantages. BPTB graft has the best tensile strength and bone union with bone, but the complications of anterior knee pain are also quite common (5-55%). Hamstring grafts and Quadriceps grafts minimize the complications of anterior knee pain, with fairly good tensile strength, but the union of grafts with bone takes longer. The loss of Hamstring tendons also causes a decrease in muscle strength in Hamstring, where Hamstring has an important role in preventing the anterior translation of the tibia Peroneus Longus Tendon graft is an alternative graft developed to minimize complications associated with graft use from the area around the knee. Peroneus Longus tendons also have tensile strength similar to Hamstring tendons. As with other graft extracts, Peroneus Longus tendon graft is also accompanied by complications in the donor site. Possible complications arising from the loss of the Peroneus Longus tendon include ankle instability and decreased flexion strength of the 1st ray and ankle eversion. Research carried out by Bancha et al showed a reduction in flexion strength of 1st ray and ankle eversion significantly, without any instability in the ankle. Peroneus longus provides 5.5% strength for moderate dorsiflexion for ankle eversion movements, peroneus longus is the main muscle. But in other studies it is said that the use of peroneus longus graft does not interfere with the stability of the ankle and ROM. Does not even affect the functional outcome of the ankle However, in a study conducted by Bancha et al and Kerimoglu et al., The technique used for taking Peroneus Longus graft tendons did not include suturing in the distal stump of Peroneous Longus. So with this study, researchers wanted to find out whether different results would be found related to donor site complications if the technique used included suturing the distal stump of the Peroneus Longus tendon against the peroneus brevis tendon
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Dec 2018
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 1, 2018
CompletedFirst Submitted
Initial submission to the registry
June 3, 2020
CompletedFirst Posted
Study publicly available on registry
June 16, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
June 30, 2022
CompletedMay 23, 2023
May 1, 2023
3 years
June 3, 2020
May 20, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (12)
Preoperative hand dynamometer value
Value of objective measurement of the strength of the medial part of the plantarflexion in the one metatarsal head with the hand of the Dynamometer when the patient is supine. The measurement is done 3 times and the value used is the average of the 3 times the measurement. Healthy ankles were also examined as a comparison with the same measurement method. There is no minimum and maximum value, and the higher value the better the outcome
This measurement was carried out at the preoperative setting
Three-months postoperative hand dynamometer value
Value of objective measurement of the strength of the medial part of the plantarflexion in the one metatarsal head with the hand of the Dynamometer when the patient is supine. The measurement is done 3 times and the value used is the average of the 3 times the measurement. Healthy ankles were also examined as a comparison with the same measurement method. There is no minimum and maximum value, and the higher value the better the outcome
This measurement was carried out at 3 months postoperatively
Six-months postoperative hand dynamometer value
Value of objective measurement of the strength of the medial part of the plantarflexion in the one metatarsal head with the hand of the Dynamometer when the patient is supine. The measurement is done 3 times and the value used is the average of the 3 times the measurement. Healthy ankles were also examined as a comparison with the same measurement method. There is no minimum and maximum value, and the higher value the better the outcome
This measurement was carried out at 6 months postoperatively
Preoperative Clark's Angle Value
the value of the objective angle measurement on the footprint by drawing a line from the medial side of the one metatarsal head and the heel against the second line which is connecting the one metatrsal head and the peak of the medial longitudinal arch. Clarke Angle of \< 31° means there is tendency to flatness and/or pronation. angle of 31° to \< 45° is the normal range. Clarke Angle of \> 45° means there is tendency to cavus foot
This measurement was carried out at the preoperative setting
Three-months Clark's Angle Value
the value of the objective angle measurement on the footprint by drawing a line from the medial side of the one metatarsal head and the heel against the second line which is connecting the one metatrsal head and the peak of the medial longitudinal arch. Clarke Angle of \< 31° means there is tendency to flatness and/or pronation. angle of 31° to \< 45° is the normal range. Clarke Angle of \> 45° means there is tendency to cavus foot
This measurement was carried out at the 3 months postoperatively
Six-months Clark's Angle Value
the value of the objective angle measurement on the footprint by drawing a line from the medial side of the one metatarsal head and the heel against the second line which is connecting the one metatrsal head and the peak of the medial longitudinal arch. Clarke Angle of \< 31° means there is tendency to flatness and/or pronation. angle of 31° to \< 45° is the normal range. Clarke Angle of \> 45° means there is tendency to cavus foot
This measurement was carried out at the 6 months postoperatively
Preoperative the American Orthopedic Foot and Ankle Score (AOFAS)
the questionnaire for assessing the function of both injured feet and ankles and the knee that is in the process of healing. AOFAS score has the range of value of 0 to 100. 0 is the worst value and 100 is the best value possible
Examination carried out 4 times for each patient in preoperative setting
Three months postoperative the American Orthopedic Foot and Ankle Score (AOFAS)
the questionnaire for assessing the function of both injured feet and ankles and the knee that is in the process of healing. AOFAS score has the range of value of 0 to 100. 0 is the worst value and 100 is the best value possible
Examination carried out 4 times for each patient in 3 months postoperatively
Six months postoperative the American Orthopedic Foot and Ankle Score (AOFAS)
the questionnaire for assessing the function of both injured feet and ankles and the knee that is in the process of healing. AOFAS score has the range of value of 0 to 100. 0 is the worst value and 100 is the best value possible
Examination carried out 4 times for each patient in 6 months postoperatively
Preoperative visual analogue scale foot and ankle (VAS-FA)
the questionnaire for assessing the function of both injured feet and ankles and the knee that is in the process of healing. VAS-FA score has the range of value of 0 to 100. 0 is the worst value and 100 is the best value possible
Examination carried out 4 times for each patient at preoperative setting
Three-months postoperative visual analogue scale foot and ankle (VAS-FA)
the questionnaire for assessing the function of both injured feet and ankles and the knee that is in the process of healing. AS-FA score has the range of value of 0 to 100. 0 is the worst value and 100 is the best value possible
Examination carried out 4 times for each patient at 3 months postoperatively
Six-months postoperative visual analogue scale foot and ankle (VAS-FA)
the questionnaire for assessing the function of both injured feet and ankles and the knee that is in the process of healing. AS-FA score has the range of value of 0 to 100. 0 is the worst value and 100 is the best value possible
Examination carried out 4 times for each patient at 6 months postoperatively
Study Arms (2)
Sutured Stump
EXPERIMENTALThe group consist of subject with distal stump suturing of perobeus longus agains peroneus brevis in ACL Reconstruction Case
Unsutured Stump
NO INTERVENTIONThe group consist of subject without distal stump suturing of peroneus longus agains peroneus brevis in ACL Reconstruction Case
Interventions
in ACL Reconstruction case , Group A consist of subject with operation procedure suturing the distal stump peroneus longus against the peroneus brevis in ACL reconstruction using the peroneus longus autograft.
Eligibility Criteria
You may qualify if:
- Patients with total ACL rupture using peroneus longus graft
- The suturing procedure for the distal stump peroneus longus against the peroneus brevis tendon is performed by orthopedic specialists or resident chiefs who have been given training in advance.
You may not qualify if:
- Osteoarthtis Knee Kellgren-Lawrence III and IV
- Osteoarthtis Knee Kellgren-Lawrence III and IV
- Flatfoot as evidenced by physical examination and footprinting
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Cipto Mangunkusumo Hospital
Jakarta, DKI Jakarta, 14250, Indonesia
Related Publications (31)
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PMID: 26920430RESULT
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- QUADRUPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Orthopaedic Surgeon
Study Record Dates
First Submitted
June 3, 2020
First Posted
June 16, 2020
Study Start
December 1, 2018
Primary Completion
December 1, 2021
Study Completion
June 30, 2022
Last Updated
May 23, 2023
Record last verified: 2023-05