Anterior Cruciate Ligament InjuryROTORNCT02310854
Acute Anterior Cruciate Ligament Rupture; RecOnsTruction Or Repair?
A study testing ACL Repair and ACL reconstruction in people with Anterior Cruciate Ligament Injury, run by Orthopedisch Centrum Oost Nederland at 1 site in Netherlands.
Trial summary
To investigate the hypothesis that suture repair of a ruptured vkb, combined with a dynamic intraligamentary stabilization and microfracture of the femoral notch, results in at least equal effectiveness compared with an ACL reconstruction using autologous hamstring in terms of functional recovery one year… Read more about this study
- Who is it for?
- Ages 18 to 30 years
- Conditions the study is for
- Anterior Cruciate Ligament Injury
- What is being tested?
- ACL Repair and ACL reconstruction
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 48 participants
- Where
- 1 siteNetherlands
- Study dates
- Nov 2014to 17 Apr 2026
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 30 years
- All sexes
- No healthy volunteers
- Adult
Who may be able to join
- Sportive, active patient (Tegner score =/>5)
- Age above 18 untill 30 years at time of inclusion
- Primary rupture of the anterior cruciate ligament, evidence by history (acute trauma, clicking sensation, swelling within a few hours, instability) and physical examination (positive Lachman, anterior drawer test and/or Pivot shift)
- Primary rupture indicated by MRI
- No associated ligamentuous disorde of the knee, evidenced by history, physical examination, x-ray or MRI)
- Time span between anterior cruciate ligament rupture and operation no longer than 21 days
- Willingness to comply to advised rehabilitation protocol supervised by (NFVS registrated) sports physiotherapist
Who cannot join
- Infection
- Known hypersensitive response for materials used (Cobalt, chroom, nickel)
- Serieus pre-existing malaligment of leg indicated for surgery
- Tendency for excessive scar tisseu formation, such as arthrofibrosis
- History of previous surgery on leg indicated for surgery
- History of removal of tendon on leg indicated for surgery
Show all 12Show fewer
- Muscular, neurological or vascular disorders negatively affecting healing or rehabilitation
- Cartilage injury requiring (some kind of) cartilage repair surgery (such as microfracture or cell therapy)
- Arthrosis more dan ICRS grade 2 evidenced by x-ray
- Long(er) term use of relevant medication, such as prednisolon or cytostatica
- Pregnancy
- Know osteoporosis
Trial locations and contacts
1 site in 1 country.
About this study
To investigate the hypothesis that suture repair of a ruptured vkb, combined with a dynamic intraligamentary stabilization and microfracture of the femoral notch, results in at least equal effectiveness compared with an ACL reconstruction using autologous hamstring in terms of functional recovery one year postoperatively in terms of a patient self-reported outcome related to be able to conduct daily and sporting activities. Secondary, the evaluation of clinical outcomes, self-reported by the patient outcomes, osteoarthritis, rehabilitation time required for return to daily and sporting activities and levels of sporting activity which has returned in patients with status after an ACL rupture and suture repair augmented with a dynamic intraligamentary microfracture and stabilization of the femoral notch in comparison with an anterior cruciate ligament reconstruction with the ipsilateral hamstring graft.
Read the detailed description
Background of the study:
An anterior cruciate ligament rupture is a serious injury to the knee with high probability of the occurrence of dynamic instability, accompanying lesions and early post-traumatic arthrosis. Despite conservative treatment through rehabilitation or ACL reconstruction surgery not all patients do return to their previous activity levels. Moreover degenerative changes, especially early posttraumatic arthrosis, are not counteracted.
In order to optimize the clinical results after ACL surgery, a renewed interest has emerged in healing the patient's own ruptured ACL after attaching. Literature suggests that with the current innovations in surgical repair techniques of (natural) healing of a ruptured ACL may result in similar clinical outcomes in comparison to the gold standard, the ACL reconstruction. In addition, it may even reduce degenerative changes occur in relation to the gold standard. Moreover, the return to daily activities and sports level seems significantly faster than after ACL reconstruction.
The hypothesis is that a suture (suture repair) of a ruptured ACL, combined with a dynamic intraligamentary stabilization, as well as microfracture of the femoral notch, passes, at least equal efficacy in comparison with an anterior cruciate ligament reconstruction using autologous hamstrings in terms of functional recovery 1 years postoperatively.
The DIS bonding technique will be applied in the current study to surgically repair (suture) the ruptured ACL. DIS is an abbreviation and stands for intraligamentary dynamic stabilization (DIS). DIS has been used in humans and seems to provide a high patient satisfaction, favorable clinical and radiological results. However, to our knowledge, to date, no randomized comparative study has been conducted yet in which the DIS technique is compared with the gold standard, the ACL reconstruction.
Objective of the study:
Primary goal:
Investigate the hypothesis that suture repair of a ruptured vkb, combined with a dynamic intraligamentary stabilization and microfracture of the femoral notch, results in at least equal effectiveness compared with an ACL reconstruction using autologous hamstring in terms of functional recovery one year postoperatively in terms of a patient self-reported outcome related to be able to conduct daily and sporting activities.
Secondary objective:
Evaluation of clinical outcomes, self-reported by the patient outcomes, osteoarthritis, rehabilitation time required for return to daily and sporting activities and levels of sporting activity which has returned in patients with status after an ACL rupture and suture repair augmented with a dynamic intraligamentary microfracture and stabilization of the femoral notch in comparison with an anterior cruciate ligament reconstruction with the ipsilateral hamstring graft.
Study design:
This study is a single center stratified block randomized controlled trial. Patients with ACL rupture, confirmed by an orthopedic surgeon based on the outpatient history and radiographic images, will be randomized into an experimental ('repair' / DIS) group after inclusion and a control (reconstruction, regular care) group. Patients will be stratified on the level of sport/physical active practice, on the basis of the Tegner score. The Tegner score is an evaluative and inventory questionnaire on which the patient indicates the gravity of his work and/or sports activities. A higher score is associated with a higher level of physical strain/activity . On the basis of the Tegner score patients will be stratified into a 'moderate' physically active stratum (group Tegner score 5-6-7) and 'highly' physically active stratum (group Tegner score 8 -9-10). Stratification based on the degree of physical activity is considered to be important because the extent and severity of physical activity/strain in daily life poses a potential (difference) in risk of re-rupture between the two study arms. In order to minimize potential differences in 'exposure' or 'risk of re-rupture' between the two study groups stratification is relevant.Measurements take place at baseline, peri-operative / immediately after surgery, 6 weeks, 3,6,9 months and 1, 2, 5 and 10 years postoperatively.
Study population: (Physically) active patients from 18 untill 30 years, who has visited the outpatient clinic of the orthopedic surgeon because of a knee injury resulting in a ACL rupture, for whom surgery indication for an ACL reconstruction exists and who can be operated on within three weeks after the onset of the ACL rupture.
Intervention:
n=48 patients will participate in the current study. Patients will be assigned to a suture repair of the ruptured vkb complemented by a dynamic intraligamentary stabilization (DIS) and microfracture of the femoral notch or the gold standard, a ACL reconstruction.
Primary study parameters/outcome of the study:
Self-reported functional outcome at one-year follow post surgery measured by the IKDC 2000 subjective scale.
Secundary study parameters/outcome of the study (if applicable):
Secondaire eindpunten: Self-reported functional outcome at one-year follow post surgery measured by the IKDC 2000 subjective scale 6 weeks, 3,6 and 9 months, 2,5 and 10 years post surgery, self-reported disabilities (KOOS), level of physical activity (Tegner), satisfaction (VAS) as well as IKDC physical examination (clinimetretrics) 6 weeks, 3, 6 en 9 months, 1, 2, 5 and 10 years post surgery; instrumented anteroposterior laxity, leg symmetry index for jump tests as well as isokinetic quadriceps en hamstrings force 6 en 9 months, 1, 2, 5 en 10 years after surgery; radiologic signs of arthrosis 1,2 5 and 10 years post surgery; reruptures of the ACL within 10 years post surgery, classification rupture pattern peroperative.
- Conditions
- Anterior Cruciate Ligament Injury
- Being tested
- ACL Repair, ACL reconstruction
- Keywords
- anterior cruciate ligament rupture, autograft, reconstruction, orthopedic surgery, dynamic intraligament stabilization
- Medical subject headings
- Anterior Cruciate Ligament Injuries
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
ACL RepairProcedure or surgery
Also called Dynamic Intraligament Stabilization (DIS), Augmented suture
augmented suture of acute ACL rupture (<3 weeks after injury)
ACL reconstructionProcedure or surgery
Also called Primary ACL reconstruction, Autograft hamstring, All-inside
reconstruction hamstring autograft
| Study group | Role | What they receive |
|---|---|---|
| ACL Reconstruction | Active comparator | Primary reconstructive surgery of ACL with hamstring autograft (All-inside, Arthrex, Napels, Florida, USA) Receives: Procedure: ACL reconstruction |
| ACL Repair | Experimental | Primary augmented suture of ACL using Dynamic Intraligament Stabilization (DIS; Mathys Medical Bettlach, Switzerland) Receives: Procedure: ACL Repair |
What is being measured
The primary outcome is the main question the study is designed to answer.
IKDC 2000 subjective knee evaluation form
questionniare/self-reported functional limitations in activitities of daily living and/or sports activities
Measured: baseline, 12 months post surgery
Secondary outcomes (6)
IKDC 2000 subjective knee evaluation form
questionnaire/self-reported functional limitations in activitities of daily living and/or sports
Measured: baseline, 6 weeks, 3-6-9-12 months, 2-5-10 years post surgery
IKDC 2000 objective knee evaluation form
knee physical examination form / clinimetrics
Measured: baseline, 6 weeks, 3-6-9-12 months, 2-5-10 years post surgery
Knee Injury and Osteoarthritis Outcome Score (KOOS)
questionnaire designed to assess short and long term patient-related ouctome following knee injury on pain, symptoms, activities of daily living, sport and recreation, knee-related quality of life
Measured: baseline, 6 weeks, 3-6-9-12 months, 2-5-10 years post surgery
Tegner Activity Level Scale
Rating scale to determine the type and intensity of sports/activities
Measured: baseline, 6 weeks, 3-6-9-12 months, 2-5-10 years post surgery
Instrumented anteroposterior laxity
Measured: baseline, 6 weeks, 3-6-9-12 months, 2-5-10 years post surgery
LSI jump-force testing
leg symmetry index for jump tests as well as isokinetic quadriceps and hamstring force tests
Measured: 6-9-12 months, 2-5-10 years post surgery
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 Dec 2014 (estimated)
- Study startNov 2014
- Primary completionApr 2026
- Study completion17 Apr 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Anterior Cruciate Ligament InjuryStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 48 participants (actual)
Sponsor and investigators
- Lead sponsor
- Orthopedisch Centrum Oost Nederland
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Judith olde Heuvel, Orthopedisch Centrum Oost Nederland
- Investigators
- R.A.G Hoogeslag, MD, Principal investigator, OCON
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02310854
- Sponsor's protocol ID
- NL5011604414
- Acronym
- ROTOR
- Status last verified
- Apr 2026
- First submitted
- 1 Dec 2014
- Last updated
- 22 Apr 2026
- Results posted
- No
- Data monitoring committee
- Yes
- Individual data sharing
- Undecided: to be determined yet
Publications
Hoogeslag RAG, Brouwer RW, Boer BC, de Vries AJ, Huis In 't Veld R. Acute Anterior Cruciate Ligament Rupture: Repair or Reconstruction? Two-Year Results of a Randomized Controlled Clinical Trial. Am J Sports Med. 2019 Mar;47(3):567-577. doi: 10.1177/0363546519825878.
PubMed 30822124Boer BC, Hoogeslag RAG, Brouwer RW, Demmer A, Huis In 't Veld RMHA. Self-reported functional recovery after reconstruction versus repair in acute anterior cruciate ligament rupture (ROTOR): a randomized controlled clinical trial. BMC Musculoskelet Disord. 2018 Apr 20;19(1):127. doi: 10.1186/s12891-018-2028-4.
PubMed 29678170
Study at a glance
From the registry record, last updated by the sponsor on 22 Apr 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Acute Anterior Cruciate Ligament Rupture; RecOnsTruction Or Repair?
- ClinicalTrials.gov ID
- NCT02310854
- Acronym / sponsor ID
- ROTOR / NL5011604414
- Conditions
- Anterior Cruciate Ligament Injury
- Keywords
- anterior cruciate ligament rupture, autograft, reconstruction, orthopedic surgery, dynamic intraligament stabilization
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 48 participants (actual)
- Lead sponsor
- Orthopedisch Centrum Oost NederlandUniversity, hospital or other
- Study start
- Nov 2014 (actual)
- Primary completion
- Apr 2026 (actual)
- Study completion
- 17 Apr 2026 (actual)
- First posted
- 8 Dec 2014 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
To investigate the hypothesis that suture repair of a ruptured vkb, combined with a dynamic intraligamentary stabilization and microfracture of the femoral notch, results in at least equal effectiveness compared with an ACL reconstruction using autologous hamstring in terms of functional recovery one year postoperatively in terms of a patient self-reported outcome related to be able to conduct daily and sporting activities. Secondary, the evaluation of clinical outcomes, self-reported by the patient outcomes, osteoarthritis, rehabilitation time required for return to daily and sporting activities and levels of sporting activity which has returned in patients with status after an ACL rupture and suture repair augmented with a dynamic intraligamentary microfracture and stabilization of the femoral notch in comparison with an anterior cruciate ligament reconstruction with the ipsilateral hamstring graft.
Detailed description
Background of the study:
An anterior cruciate ligament rupture is a serious injury to the knee with high probability of the occurrence of dynamic instability, accompanying lesions and early post-traumatic arthrosis. Despite conservative treatment through rehabilitation or ACL reconstruction surgery not all patients do return to their previous activity levels. Moreover degenerative changes, especially early posttraumatic arthrosis, are not counteracted.
In order to optimize the clinical results after ACL surgery, a renewed interest has emerged in healing the patient's own ruptured ACL after attaching. Literature suggests that with the current innovations in surgical repair techniques of (natural) healing of a ruptured ACL may result in similar clinical outcomes in comparison to the gold standard, the ACL reconstruction. In addition, it may even reduce degenerative changes occur in relation to the gold standard. Moreover, the return to daily activities and sports level seems significantly faster than after ACL reconstruction.
The hypothesis is that a suture (suture repair) of a ruptured ACL, combined with a dynamic intraligamentary stabilization, as well as microfracture of the femoral notch, passes, at least equal efficacy in comparison with an anterior cruciate ligament reconstruction using autologous hamstrings in terms of functional recovery 1 years postoperatively.
The DIS bonding technique will be applied in the current study to surgically repair (suture) the ruptured ACL. DIS is an abbreviation and stands for intraligamentary dynamic stabilization (DIS). DIS has been used in humans and seems to provide a high patient satisfaction, favorable clinical and radiological results. However, to our knowledge, to date, no randomized comparative study has been conducted yet in which the DIS technique is compared with the gold standard, the ACL reconstruction.
Objective of the study:
Primary goal:
Investigate the hypothesis that suture repair of a ruptured vkb, combined with a dynamic intraligamentary stabilization and microfracture of the femoral notch, results in at least equal effectiveness compared with an ACL reconstruction using autologous hamstring in terms of functional recovery one year postoperatively in terms of a patient self-reported outcome related to be able to conduct daily and sporting activities.
Secondary objective:
Evaluation of clinical outcomes, self-reported by the patient outcomes, osteoarthritis, rehabilitation time required for return to daily and sporting activities and levels of sporting activity which has returned in patients with status after an ACL rupture and suture repair augmented with a dynamic intraligamentary microfracture and stabilization of the femoral notch in comparison with an anterior cruciate ligament reconstruction with the ipsilateral hamstring graft.
Study design:
This study is a single center stratified block randomized controlled trial. Patients with ACL rupture, confirmed by an orthopedic surgeon based on the outpatient history and radiographic images, will be randomized into an experimental ('repair' / DIS) group after inclusion and a control (reconstruction, regular care) group. Patients will be stratified on the level of sport/physical active practice, on the basis of the Tegner score. The Tegner score is an evaluative and inventory questionnaire on which the patient indicates the gravity of his work and/or sports activities. A higher score is associated with a higher level of physical strain/activity . On the basis of the Tegner score patients will be stratified into a 'moderate' physically active stratum (group Tegner score 5-6-7) and 'highly' physically active stratum (group Tegner score 8 -9-10). Stratification based on the degree of physical activity is considered to be important because the extent and severity of physical activity/strain in daily life poses a potential (difference) in risk of re-rupture between the two study arms. In order to minimize potential differences in 'exposure' or 'risk of re-rupture' between the two study groups stratification is relevant.Measurements take place at baseline, peri-operative / immediately after surgery, 6 weeks, 3,6,9 months and 1, 2, 5 and 10 years postoperatively.
Study population: (Physically) active patients from 18 untill 30 years, who has visited the outpatient clinic of the orthopedic surgeon because of a knee injury resulting in a ACL rupture, for whom surgery indication for an ACL reconstruction exists and who can be operated on within three weeks after the onset of the ACL rupture.
Intervention:
n=48 patients will participate in the current study. Patients will be assigned to a suture repair of the ruptured vkb complemented by a dynamic intraligamentary stabilization (DIS) and microfracture of the femoral notch or the gold standard, a ACL reconstruction.
Primary study parameters/outcome of the study:
Self-reported functional outcome at one-year follow post surgery measured by the IKDC 2000 subjective scale.
Secundary study parameters/outcome of the study (if applicable):
Secondaire eindpunten: Self-reported functional outcome at one-year follow post surgery measured by the IKDC 2000 subjective scale 6 weeks, 3,6 and 9 months, 2,5 and 10 years post surgery, self-reported disabilities (KOOS), level of physical activity (Tegner), satisfaction (VAS) as well as IKDC physical examination (clinimetretrics) 6 weeks, 3, 6 en 9 months, 1, 2, 5 and 10 years post surgery; instrumented anteroposterior laxity, leg symmetry index for jump tests as well as isokinetic quadriceps en hamstrings force 6 en 9 months, 1, 2, 5 en 10 years after surgery; radiologic signs of arthrosis 1,2 5 and 10 years post surgery; reruptures of the ACL within 10 years post surgery, classification rupture pattern peroperative.
Study design
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| ACL Reconstruction | Active comparator | Procedure: ACL reconstructionPrimary reconstructive surgery of ACL with hamstring autograft (All-inside, Arthrex, Napels, Florida, USA) |
| ACL Repair | Experimental | Procedure: ACL RepairPrimary augmented suture of ACL using Dynamic Intraligament Stabilization (DIS; Mathys Medical Bettlach, Switzerland) |
Who may qualify
- Ages
- 18 to 30 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult
Key inclusion criteria (7 listed)
- Sportive, active patient (Tegner score =/>5)
- Age above 18 untill 30 years at time of inclusion
- Primary rupture of the anterior cruciate ligament, evidence by history (acute trauma, clicking sensation, swelling within a few hours, instability) and physical examination (positive Lachman, anterior drawer test and/or Pivot shift)
- Primary rupture indicated by MRI
- No associated ligamentuous disorde of the knee, evidenced by history, physical examination, x-ray or MRI)
Key exclusion criteria (12 listed)
- Infection
- Known hypersensitive response for materials used (Cobalt, chroom, nickel)
- Serieus pre-existing malaligment of leg indicated for surgery
- Tendency for excessive scar tisseu formation, such as arthrofibrosis
- History of previous surgery on leg indicated for surgery
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| ACL RepairAlso: Dynamic Intraligament Stabilization (DIS), Augmented sutureaugmented suture of acute ACL rupture (<3 weeks after injury) | Procedure or surgery | ACL Repair |
| ACL reconstructionAlso: Primary ACL reconstruction, Autograft hamstring, All-insidereconstruction hamstring autograft | Procedure or surgery | ACL Reconstruction |
Primary outcome
IKDC 2000 subjective knee evaluation form
Time frame: baseline, 12 months post surgery
questionniare/self-reported functional limitations in activitities of daily living and/or sports activities
6 secondary outcomes
IKDC 2000 subjective knee evaluation form
Time frame: baseline, 6 weeks, 3-6-9-12 months, 2-5-10 years post surgery
IKDC 2000 objective knee evaluation form
Time frame: baseline, 6 weeks, 3-6-9-12 months, 2-5-10 years post surgery
Knee Injury and Osteoarthritis Outcome Score (KOOS)
Time frame: baseline, 6 weeks, 3-6-9-12 months, 2-5-10 years post surgery
Tegner Activity Level Scale
Time frame: baseline, 6 weeks, 3-6-9-12 months, 2-5-10 years post surgery
Instrumented anteroposterior laxity
Time frame: baseline, 6 weeks, 3-6-9-12 months, 2-5-10 years post surgery
LSI jump-force testing
Time frame: 6-9-12 months, 2-5-10 years post surgery
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 22 Apr 2026.
- Derived from this study: PubMed 30822124Hoogeslag RAG, Brouwer RW, Boer BC, de Vries AJ, Huis In 't Veld R. Acute Anterior Cruciate Ligament Rupture: Repair or Reconstruction? Two-Year Results of a Randomized Controlled Clinical Trial. Am J Sports Med. 2019 Mar;47(3):567-577. doi: 10.1177/0363546519825878.
- Derived from this study: PubMed 29678170Boer BC, Hoogeslag RAG, Brouwer RW, Demmer A, Huis In 't Veld RMHA. Self-reported functional recovery after reconstruction versus repair in acute anterior cruciate ligament rupture (ROTOR): a randomized controlled clinical trial. BMC Musculoskelet Disord. 2018 Apr 20;19(1):127. doi: 10.1186/s12891-018-2028-4.
- Individual participant dataSharing planned: Undecided. to be determined yet
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
R.A.G Hoogeslag, MD principal investigator
OCON
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing ACL Repair and ACL reconstruction in people with Anterior Cruciate Ligament Injury, run by Orthopedisch Centrum Oost Nederland at 1 site in Netherlands.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 7 inclusion and 12 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 22 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Netherlands. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
IKDC 2000 subjective knee evaluation form (time frame: baseline, 12 months post surgery). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT02310854, which also lists 2 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Apr 2026.