Internal Fixation Clinical Trials

2 recruiting

Frequently Asked Questions

Common questions about Internal Fixation clinical trials

A clinical trial is a carefully designed research study that tests new medical treatments, drugs, devices, or approaches in human volunteers. Every approved medication and treatment available today was proven safe and effective through clinical trials.

All clinical trials are reviewed and approved by Institutional Review Boards (IRBs) — independent committees that evaluate patient safety. Trials follow strict protocols, and your health is monitored closely throughout. You can withdraw at any time.

Not necessarily. Many trials compare the new treatment against the current standard of care, meaning all participants receive active treatment. When placebos are used, they are typically combined with standard treatment, not given alone. The trial description will always specify the design.

Under the Affordable Care Act, most private insurers are required to cover routine patient care costs during a clinical trial. The sponsor typically covers the investigational treatment itself. Medicare also covers routine costs for qualifying trials.

Yes. Participation is completely voluntary. You can withdraw at any time, for any reason, without it affecting your access to standard medical care.

Each trial has specific eligibility criteria — including age, diagnosis, disease stage, prior treatments, and general health. Browse the trials listed above and check their eligibility sections. You can also contact the trial site directly to discuss your situation.

Showing 17 of 7 trials

Recruiting
Not Applicable

Evaluation of Fracture Migration After Internal Fixation of Femoral Neck Fractures in Younger Adults: A Clinical RCT Using RSA

Hip FracturesFemoral Neck FracturesInternal Fixation; Complications
Odense University Hospital75 enrolled4 locationsNCT06521671
Recruiting
Not Applicable

Early Internal Fixation Versus NonOperative Care With Early Rehabilitation for LC1 Fragility Fractures of the Pelvis

Fragility FractureInternal FixationMultiple Closed Pelvic Fractures With Disruption of Pelvic Ring+1 more
University of Southern California48 enrolled13 locationsNCT06496867
Recruiting
Not Applicable

Functional Outcome After ORIF or Arthroplasty for Femoral Neck Fracture

Hip FracturesArthroplasty ComplicationsTreatment Complication+3 more
Uppsala University340 enrolled1 locationNCT06152198
Recruiting
Not Applicable

Inmobilization With Compression Bandage vs Antebraquial Splint in Distal Radius Fractures

Distal Radius FracturesInternal Fixation; Complications, Mechanical
Hospital Costa del Sol120 enrolled2 locationsNCT06019585
Recruiting
Not Applicable

Three Cancellous Screws Versus Four Cancellous Screws for Femoral Neck Fixation

Femoral Neck FracturesInternal Fixation
Peking University Third Hospital290 enrolled1 locationNCT04869332
Recruiting

A prospective, randomised study comparing the use of Actifuse (trademark) Advanced Bone MatriX (ABX) synthetic bone substitute with INFUSE (registered trademark) in patients requiring posterolateral instrumented lumbar fusion.

Degenerative disc disease that can be treated using Posterolateral Intertransverse Process Fusion and Internal Fixation achieved by pedicle screws and rods.
ApaTech Ltd100 enrolled1 locationACTRN12609000548235
Recruiting

A prospective, randomised study comparing the use of Actifuse (trademark) Advanced Bone MatriX (ABX) synthetic bone substitute with INFUSE (registered trademark) in patients requiring posterolateral instrumented lumbar fusion with interbody fusion

Degenerative disc disease that can be treated using Posterior Lumbar Interbody Fusion with Posterolateral Intertransverse Process Fusion and Internal Fixation achieved by pedicle screws and rods.
ApaTech Ltd100 enrolled1 locationACTRN12609000527268