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Not yet recruitingNCT06980285Updated May 20, 2025

Comparison of Quadriceps and Semitendinosus Grafts in ACL Reconstruction Using Data From the Danish Knee Ligament Reconstruction Registry (DKRR)

An observational study in Anterior Cruciate Ligament Injury, Knee Injury and Ligament Reconstruction, sponsored by Abdirahman Hassan Omar. Not yet recruiting at 1 site in Denmark. Open to participants aged 15 Years to 50 Years. Per ClinicalTrials.gov, last updated 2025-05-20.

Sponsored by Abdirahman Hassan Omar · Observational

From the registry’s dates

  • Primary completion was expected by Sep 2025, 1 year ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
2,500
Ages
15 Years to 50 Years
Sex
All
01

Study summary

This study looks at two different types of tendon (tissue) used in knee surgery to repair a torn anterior cruciate ligament (ACL), which is a common injury in active people. The two types are taken from different muscles in the thigh: one from the front (quadriceps) and one from the back (semitendinosus). We will use information already collected in a national health registry to see how patients recover after surgery. The study will compare knee function, activity level, and how often patients need another operation.

Read the detailed description

This is a retrospective observational cohort study based on data from the Danish Knee Ligament Reconstruction Registry (DKRR). The study includes patients who underwent primary ACL reconstruction using either a quadriceps tendon graft (with or without a bone block) or a quadrupled semitendinosus tendon graft. The primary outcome measures are the Knee Injury and Osteoarthritis Outcome Score (KOOS) and the Tegner Activity Scale. Secondary outcomes include reoperation rates, postoperative complications, and patient satisfaction. All available demographic, operative, and patient-reported outcome data will be analyzed. Multivariable regression will be used to adjust for confounders such as age, sex, BMI, time from injury to surgery, and surgeon volume. The study is exempt from ethical approval under Danish law, and data will be handled in compliance with GDPR.

02

Conditions studied

  • Anterior Cruciate Ligament Injury
  • Knee Injury
  • Ligament Reconstruction
  • Sports Injuries

Keywords

  • ACL reconstruction
  • Quadriceps tendon graft
  • Semitendinosus graft
  • DKRR
  • Knee ligament injury
  • Orthopaedic surgery
  • Registry study
03

In context

Anterior Cruciate Ligament Injuries

521 studies on the registry are indexed under Anterior Cruciate Ligament Injuries; 169 are open to participants now.

This study's planned enrollment of 2,500 is above the median of 96 across 131 observational studies indexed under Anterior Cruciate Ligament Injuries.

Browse Anterior Cruciate Ligament Injuries studies →

Lead sponsor

This is the only study on the registry with Abdirahman Hassan Omar as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
15 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients registered in the Danish Knee Ligament Reconstruction Registry (DKRR) who underwent primary anterior cruciate ligament reconstruction using either a quadriceps tendon graft or a semitendinosus tendon graft. All included patients have completed at least one year of follow-up and patient-reported outcome measures. The population consists of physically active individuals aged 15 to 50 years.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Primary ACL reconstruction registered in the Danish Knee Ligament Reconstruction Registry (DKRR)
  • Known graft type: quadriceps tendon or semitendinosus tendon Minimum 1-year follow-up with completed patient-reported outcome measures (KOOS and/or Tegner score)
  • Age between 15 and 50 years at the time of surgery (optional subgroup analysis)

Exclusion criteria

Exclusion Criteria:

  • Revision ACL reconstruction
  • Multiligament knee reconstruction
  • Missing or incomplete PROMs or key clinical data
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
2,500 participants (estimated)
Patient registry
No

Groups and cohorts

  • Quadriceps tendon graft

    Patients who underwent primary ACL reconstruction using a quadriceps tendon autograft, with or without a bone block. Data are derived retrospectively from the Danish Knee Ligament Reconstruction Registry (DKRR).

  • Semitendinosus graft

    Patients who underwent primary ACL reconstruction using a quadrupled semitendinosus tendon autograft. Data are derived retrospectively from the Danish Knee Ligament Reconstruction Registry (DKRR).

06

What researchers measure

Primary outcomes

  1. The Knee Injury and Osteoarthritis Outcome Score (KOOS)

    The Knee Injury and Osteoarthritis Outcome Score (KOOS) evaluates pain, symptoms, daily living, sport/recreation, and knee-related quality of life. Metric type: continuous PROM-based subscale score Method of measurement: Self reported questionnaire

    Time frame: At minimum 1 year follow up postoperatively

  2. Tegner Activity Score

    Assesses patients' level of physical activity before injury and at follow-up. Metric type: Scale from 0-10, where 0 is no physical activity caused by knee problems and 10 is an ability to compete in elite level sport like soccer and ski. Method of measurement: Tegner scale, self reported

    Time frame: Minimum 1 year follow up postoperatively.

Secondary outcomes

  1. Re-operation rate

    Incidence of surgical re-intervention after primary ACL reconstruction. Method of measurement: Registry recorded re-operations in DKRR

    Time frame: Within 1 year of surgery

  2. Postoperative complications

    Frequency of postoperative complications such as infection, stiffness, or graft failure. Metric type: Occurrence of postoperative complications Method of measurement: Clinically reported and registry documented complications in DKRR

    Time frame: Within 1 year after surgery

  3. Patient satisfaction

    Overall patient satisfaction with surgical outcome, if available in registry. Metric type: PROM's available from the DKRR Method of measurement: Patient reported satisfaction score.

    Time frame: 1 year follow up

07

Study locations

1 site
  • Søernes Privathospital
    Copenhagen, Frederiksberg 1900, Denmark
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Jun 2025; primary completion for Sep 2025, 3 months later.

How these figures are worked out, and which studies are left out of them.

Registered
May 12, 2025
First posted
May 20, 2025
StartEst.
Jun 1, 2025
Primary completionEst.
Sep 30, 2025
CompletionEst.
Nov 30, 2025
Last update
May 20, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 20, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06980285
Lead sponsor
Abdirahman Hassan Omar
Collaborators
Søernes Privathospital
Responsible party
Abdirahman Hassan Omar (Medical student, Principal incestigator, Søernes Privathospital) — Sponsor-investigator
First posted
May 20, 2025
Start date
Jun 1, 2025 (estimated)
Primary completion
Sep 30, 2025 (estimated)
Completion
Nov 30, 2025 (estimated)
Last update
May 20, 2025

Study contacts

Abdirahman Omar H Medical Students
Contact
Namharidba2@gmail.com
+ 45 27 59 97 29
Mikkel Attrup L MD, Orthopedic Surgeon
Contact
Mikkel@attrup.dk

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in May 2025. You cannot join it, but the record below documents what was studied.

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