- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04453592
Adductor Longus Tenotomy & the BKFO Test
The Effect of an Adductor Longus Tenotomy on the Bent Knee Fall Out Test
The bent knee fall out test (BKFO) is a common test for hip adductor flexibility. It is unknown whether the BKFO actually tests the the adductors or potentially hip range of motion instead.
In this study, the BKFO test is performed in the operating theater before and after an adductor longus tenotomy.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Adductor-related groin pain is the most common type of groin pain in athletes, and pain at the proximal adductor longus insertion is a key finding in the diagnosis of longstanding groin pain. "Tightness" or "shortening" of the adductor longus is considered both a cause and effect of pain, that can lead to increased tension at the proximal insertion, thus playing a role in the persistence of longstanding adductor-related pain. For patients who do not respond sufficiently to non-surgical procedures, an adductor longus tenotomy is a surgical option that is considered to reduce tension at the proximal adductor longus insertion assisting in reduction of pain and return to sport.
The bent knee fall out test (BKFO) is one of the most commonly used tests to test adductor flexibility. This test involves a combined hip movement with hip flexion, abduction, and external rotation, and a high result is generally considered to be related to adductor muscle "tightness", specifically that of the adductor longus. It is uncertain whether the BKFO test is actually measuring adductor muscle flexibility or hip joint range of motion, as the test results may also be affected by a femoral head cam morphology. A slightly different test, called the Patrick FABER's test, involves a similar movement and is mainly used as a hip joint pain provocation test.
By cutting the adductor longus tendon, thereby removing the effect of potential adductor longus "tightness", it will be possible to show if and how much the flexibility of this muscle affects the BKFO test results. This will assist in future considerations of what this test is actually testing.
The aim of this study is to investigate the immediate effect of an adductor longus tenotomy on the results of the bent knee fall out test.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Merignac, France, 33700
- Clinique du sport Bordeaux - Mérignac
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- adults (>18 years old)
- athletes (recreational or elite)
- clinical diagnosis of adductor-related groin pain
- patients undergoing unilateral or bilateral adductor longus tenotomy by one general surgeon.
Exclusion Criteria:
- No specific exclusion criteria were present other than refusal to participate in the study.
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Only
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in the Bent Knee Fall Out test
Time Frame: Baseline pre-surgery and immediately after the surgery.
|
The patient lies supine on the surgical table with app.
90° knee flexion, 45° hip flexion, and the feet together and the hips in external rotation (also known as the frog-leg position.
Standardization of position is achieved by flexing one leg first, so the medial malleolus is placed next to the medial knee joint line of the contra-lateral leg.
The knee is then moved laterally, externally rotating the hip with the plantar surface placed towards the contra-lateral leg.
The contra-lateral leg is then flexed, and the plantar surfaces of the feet are aligned.
The distance between the most distal point on the head of the fibula and the surface of the surgical table is measured using a rigid tape measure and distance is recorded in cm to the nearest 0.5 cm
|
Baseline pre-surgery and immediately after the surgery.
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ALTBKFO
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Adductor Tendinitis
-
AspetarUniversity College DublinCompletedHip Pain Chronic | Inguinal Hernia | Groin Injury | Iliopsoas Syndrome | Adductor TendinitisQatar
-
Dublin City UniversityNot yet recruitingAdductor StrainIreland
-
Cairo UniversityNot yet recruitingAdductor Canal Block
-
Women's College HospitalCompletedAnesthesia | Adductor Canal BlockCanada
-
Assiut UniversityCompletedSingle-shot Adductor Canal Block With Levobupivacaine and Dexmedetomidine in Total Knee ArthroplastyDexmedetomidine | Levobupivacaine | Adductor Canal BlockEgypt
-
University of Colorado, DenverUniversity of Newcastle, AustraliaWithdrawnBicep Tendinitis | Biceps; Tenosynovitis | Bicipital Tendinitis, Left Shoulder | Bicipital Tendinitis, Right Shoulder | Bicipital Tendinitis, Unspecified Shoulder | Biceps Tendon DisorderUnited States
-
University of IowaCompletedAdductor Canal Block | Postop Analgesia for KneeUnited States
-
National Cheng-Kung University HospitalRecruitingArthroplasty, Replacement, Knee | Adductor Canal BlockTaiwan
-
Poitiers University HospitalCompletedObservation of Neuromuscular Block | Flexor Hallucis | Adductor PollicisFrance
-
University of MiamiWithdrawnArthroplasty Complications | Opioid Use | Peripheral Nerve Block | Adductor Canal Block
Clinical Trials on No intervention assigned as part of this study.
-
University of Colorado, DenverCompleted
-
Biosplice Therapeutics, Inc.Completed
-
University of AberdeenRecruitingLichen Planus, Oral | Lichen Planus of VulvaUnited Kingdom
-
Aga Khan University Hospital, PakistanCompleted
-
Kardium Inc.St. Paul's Hospital, CanadaCompletedAtrial FibrillationCanada
-
German Cancer Research CenterCompletedMyocardial Infarction | Stroke | Cardiovascular MortalityGermany
-
Chinese University of Hong KongNot yet recruiting
-
Xuanwu Hospital, BeijingActive, not recruiting
-
Nicoline LøkkenCompleted
-
Usona InstituteTerminatedMajor Depressive DisorderUnited States