Pelvis RCT: Impact of Surgery on Pain in Lateral Compression Type Pelvic Fractures
Completed · Not applicable
Conditions studied: LC Pelvic Fracture
In brief
Lateral compression type pelvic ring injuries remain the most common type of pelvic fractures encountered. There is a substantial amount of controversy surrounding the treatment of these injuries and there is evidence that both operative and non-operative treatment can be successful.
Key facts
- Study ID
- NCT02625766
- Run by
- University of Maryland, Baltimore
- People needed
- 95
- Starts
- 2015-04-20
- Expected to finish
- 2020-12-31
- Last updated by the study team
- 2022-05-09
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- The patient has one of the following pelvic fractures (includes bilateral sacral fractures): Lateral compression type 1, Lateral compression type 2, Lateral compression type 3
- The patient is between 18 and 80 years of age, inclusive
- The patient has reached skeletal maturity
- The patient's pelvic fracture is a result of trauma (includes polytraumatized patients)
- The patient/family/guardian is English-speaking
- The patient's surgeon agrees to randomization (the patient is amendable to either operative or non-operative treatment)
- Patient enrollment and, if applicable, patient randomization can occur within 96 hours post injury
You may not qualify if…
- The patient has prior surgical hardware in place that precludes intervention
- The patient's pelvic fracture is classified as a Lateral compression type 1 and the associated sacral fracture is incomplete as indicated by failure to violate both the anterior and posterior cortex
- The patient received prior surgical intervention for his/her current pelvic injury
- The patient has sacral morphology that precludes percutaneous fixation
- The patient is non-ambulatory due to an associated spinal cord injury
- The patient was non-ambulatory pre-injury
- The patient is currently pregnant
- The patient is enrolled in another research study that does not allow co-enrollment
- The patient is likely to have severe problems with maintaining follow-up
Where it is running
- Indiana University Health — Indianapolis, Indiana, United States
- University of Maryland, Shock Trauma Center — Baltimore, Maryland, United States
Full record on ClinicalTrials.gov
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