- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03193840
Posterior Wall Osteotomy for Old Acetabular Fracture (osteotomy)
Surgical Treatment of Old Acetabular Fracture With Posterior Wall Osteotomy
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
More and more patients with old acetabular fracture were admitted in our institution during the past years. There is little literature especially depicts the therapeutic principle of the kind of damage. Posterior wall osteotomy would be conducted to eliminate the fragments or callus from the hip joint. Then, the deformed healing acetabulum could become mobile and the reduction may be achieved. However, the surgical procedure is technique demanding and some intraoperative risk may be accompanied.
Surgical time, blood loss, complication and fracture healing would be reviewed to assess the feasibility of the surgical procedure. The function outcome is evaluated with HHS score at the follow up.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Hebei
-
Shijiazhuang, Hebei, China, 050051
- Recruiting
- Hebei medical university third hospital
-
Shijiazhuang, Hebei, China, 050051
- Recruiting
- Zhiyong Hou
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- acetabular fracture
- no surgical procedure has been obtained over 3 weeks
- deformed healing
- receive posterior wall osteotomy
- completed more than one year follow-up
Exclusion Criteria:
- accompanied with other fracture
- pathological fracture
- reject the posterior wall osteotomy
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: NA
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: old acetabular fracture
posterior wall osteotomy would be conducted for thr patient with displaced acetabular fracture without surgical treatment over three weeks.
|
posterior wall osteotomy is conducted through Kocher-Langenbeck approach.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
frecture union time
Time Frame: 4 months
|
the fracture line in the radiography
|
4 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
complication
Time Frame: 1 month
|
iatrogenic neurovascular injury
|
1 month
|
Collaborators and Investigators
Investigators
- Study Chair: Zhiyong Hou, Third Hospital of Hebei Medical University Department of Orthopaedic Surgery
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ZRP1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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