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NCT06238804 Clinical Trial

Characteristic Analysis and Surgical Exploration for Acetabular Roof Fractures: Multicenter Retrospective Cohort Study

Acetabular Fracture Clinical Trial

— CASEARF  

Official title:
Characteristic Analysis and Surgical Exploration for Acetabular Roof Fractures: Multicenter Retrospective Cohort Study

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT06238804
Other study ID # ZRP2024
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date January 1, 2024
Est. completion date May 1, 2024

Study information
Verified date April 2024
Source Hebei Medical University Third Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Acetabular roof was a crucial structure for maintaining the stability of hip joint; however, its important role was not especially emphasized in the Letournel-Judet classification system. Acetabular roof was segmented into the roof column and roof wall in Three-column classification and fracture in this area alone was defined as A3 injury. Radiographic data and functional outcome of A3 injury patients were reviewed to explore the characteristics and surgical strategy.

Description:

Fracture data, surgical incision, operation time, blood loss, fracture healing， Reduction quality，functional outcome，and relevant complications

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date May 1, 2024
Est. primary completion date May 1, 2024
Accepts healthy volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - 18-80 years, acute (<14 days) closed roof column/wall acetabular fractures (A3.1, A3.2 or A3.3) in Three-column classification, normal activity of the affected hip before the injury, received surgical reduction and internal fixation Exclusion Criteria: - open fractures, pathologic fractures, limited range of motion (ROM) of the hip joint before the injury, conservative treatment, risk factors affecting bone healing (such as smoking and metabolic diseases) and noncompletion of the two-year follow-up

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• KL, Iliofemoral, Ilioinguinal, Iliac fossa and combined approaches
A3.1, A3.2, A3.3

Locations
Country Name City State
China Hebei Medical University Third Hospital Shijiazhuang Hebei

Sponsors (1)
Lead Sponsor Collaborator
Hebei Medical University Third Hospital

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary postoperative outcome Merle d'Aubigné score, fracture healing, reduction quality, etc 4 months
Secondary complication wound infection, iatrogenic injury of vessels and nerves, etc 1 month
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