Modifications of Devices for Hip Arthroscopy

This study is testing improved surgical tools for hip arthroscopy, a procedure to treat hip problems. The researchers have modified a "hip capsule side fixed slotted cannula" for better access to the hip joint and a "bone graft delivery tool set" for treating cysts during surgery. They want to see if these modified tools can make surgeries faster. You might be able to join if you are between 18 and 60 years old, have ongoing hip pain from conditions like FAI (femoroacetabular impingement) or hip dysplasia, and haven't found relief from other treatments. The study aims to enroll 111 participants, but its current status is unclear.

Study design
This is an interventional study, meaning participants will receive a specific treatment. It plans to enroll 111 participants.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Surgical time will be measured at 1 day after the procedure.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT04516109

Modifications of Devices for Hip Arthroscopy

UNKNOWN
NAAges 18–60InterventionalTreatment
University of Colorado, Denver
~111 participants
Updated 2023-02-08 on ClinicalTrials.gov
What's tested:Modified hip capsule side fixed slotted cannulaModified bone graft delivery tool set

At a glance

Recruiting sites
0 of 2 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Surgical time per technical phase measured in minutes
Measured over 1 Day
Hip Arthroscopy

NCT04516109

Where you'd take part

This study runs at 2 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • UCHealth Steadman Hawkins Clinic - Denver

    Englewood, Coloradono site contact published

  • University of Colorado, Hip Preservation Center, Orthopedic Department

    Boulder, Coloradono site contact published

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

  • Omer Mei-Dan, MD · PRINCIPAL_INVESTIGATOR · University of Colorado, Denver

This trial hasn't published a contact. View it on ClinicalTrials.gov

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Eligibility criteria

Inclusion

Males or females between the ages of 18 and 60 years diagnosed with FAI, Hip Dysplasia or the combination of the two.
Persistent hip pain accompanied by mechanical symptoms refractory to nonoperative management lasting at least 3 months.
Reproducible clinical examination findings suggestive of impingement and/or decreased range of motion, and positive radiographic findings on radiography, computed tomography with 3-dimensional reconstruction, and magnetic resonance imaging.
Joint-space width \> 3 mm on all views of plain radiography and 3-dimensional computed tomography.
Patients undergoing hip arthroscopy for the treatment of FAI, Hip Dysplasia, or the combination of the two by the Principal Invesitgator.

Exclusion

Age \<18 years.
Prisoners.
Pregnant women.
Decisionally challenged.
Does not speak or understand English.
  • Surgical time per technical phase measured in minutes1 Day

    * We aim to demonstrate that the use of the modified device for hip arthroscopy is fast and efficient as measured by surgical time per technical phase (i.e. arthroscopic labral repair phase and arthroscopic bone grafting phase). * Arthroscopic Labral Repair Phase: During hip arthoscopy, the surgical time of the arthroscopic labral repair phase will be collected. * Arthroscopic Bone Grafting Phase: During hip arthoscopy, the surgical time of the bone grafting of the hip joint phase will be collected. * In this design, the technical phase recorded will either be: 1) duration of arthroscopic labral repair phase (in patients only undergoing arthroscopic labral repair) or 2) duration of arthroscopic bone grafting phase (in patients undergoing arthroscopic bone grafting).