Observing recovery in patients with pelvic and acetabular fractures
Functional, Clinical, and Performance Outcomes Following Pelvic and Acetabular Fracture: A Prospective Observational Study
This study looks at how different treatments for pelvic and acetabular fractures affect recovery and quality of life for patients over time.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 200 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Wake Forest University Health Sciences Academic / other |
| Locations | 1 site (Charlotte, North Carolina) |
| Trial ID | NCT04615104 on ClinicalTrials.gov |
What this trial studies
This study aims to collect and analyze data from patients who have sustained pelvic and acetabular fractures, whether treated surgically or non-surgically. By utilizing the NIH PROMIS tool, the study will assess functional outcomes and patient-reported experiences over time. The goal is to understand how different treatment approaches affect recovery and quality of life for these patients. This observational study will provide valuable insights into the effectiveness of various treatment methods.
Who should consider this trial
Good fit: Ideal candidates include individuals with fractures of the pelvic ring or acetabulum who are willing to provide consent.
Not a fit: Patients with fractures who are unwilling to participate in the study will not benefit from its findings.
Why it matters
Potential benefit: If successful, this study could improve treatment strategies and recovery outcomes for patients with pelvic and acetabular fractures.
How similar studies have performed: While similar observational studies have been conducted, this specific approach to understanding functional outcomes in pelvic and acetabular fractures is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Fracture of the pelvic ring * Fracture of the acetabulum Exclusion Criteria: * Patients unwilling to provide consent to participate.
Where this trial is running
Charlotte, North Carolina
- Atrium Health- Carolinas Medical Center — Charlotte, North Carolina, United States (Recruiting)
Study contacts
- Principal investigator: Madhav Karunakar, MD — Wake Forest University Health Sciences
- Study coordinator: Christine Churchill, MA
- Email: Christine.Churchill@advocatehealth.org
- Phone: 7043556947
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.