Clinical Trials Logo

Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT02327949
Other study ID # HZY-0001
Secondary ID
Status Active, not recruiting
Phase Phase 4
First received December 20, 2014
Last updated August 15, 2016
Start date December 2014
Est. completion date March 2017

Study information

Verified date August 2016
Source Hebei Medical University Third Hospital
Contact n/a
Is FDA regulated No
Health authority China: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether this new W-Shaped Angular Plate is more effective and more safe to operate than the traditional reconstruction plate in the treatment of the posterior wall fracture of acetabulum.


Description:

The posterior acetabular wall fracture is one of the simpler acetabular fracture patterns and the most common type, accounting for approximately one quarter of all acetabular fractures. Most patients achieve excellent outcomes after anatomical reduction and rigid internal fixation with standard screws and buttress plates.However,it is well known that the reconstruction plate need remould in the surgery. So it does not only lead to the extension of operation time, but also cause poor attach of acetabular posterior wall. Moreover, the angulation of the screw placement for the holes of the reconstruction plate in the danger zone was determined with only caution. The intraoperative fluoroscopy was employed frequently to help determine the periacetabular screw location. If the operator lack of experience, intraarticular screw penetration and prolonged operative duration is inevitable. The investigators now introduce a new type of internal fixation device of acetabular posterior wall fracture that improve the shortcomings of existing technology.The plate itself can be thought to consist of three regions: the iliac region, the danger zone region, and the ischial tuberosity region. The organization of these regions causes the plate to resemble the English alphabet letter ''W''.The contour and zygomorphy of the W-shaped plate matched the surface of the posterior column of the acetabulum. There are two rows of drill holes in the danger zone region. A special safe-angled drilling guide was used to assist in the operation. A retrospective study has been indicated that this kind of new plate produce good results. This device may help to avoid intraarticular screw penetration and reduce operative duration and blood loss. The device further provides a stable fixation of the posterior wall that is amenable to early range of motion and weight bearing postoperatively, and results in a good clinical outcome.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 40
Est. completion date March 2017
Est. primary completion date March 2017
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Male or female aged 18 years or older(with no upper age limit)

- Sustained a posterior acetabular wall fracture(ASIF/OTA classification 62-A1)

- Operation was performed within 14 days after the fracture occurring

Exclusion Criteria:

- Presented with a pathologic acetabular fracture

- Neuropathic arthropathy,dementia and other disease processes which made postoperative compliance unreliable

- Refused to participate

- Patients who were unable to walk before injury

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Device:
W-Shaped Angular Plate
Treatment of posterior wall fracture of the acetabulum with a W-Shaped Angular Plate
Reconstruction Plate
Treatment of posterior wall fracture of the acetabulum with a Reconstruction Plate

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 Reduction quality of fracture Based on the radiographic grade criteria developed by Matta Six months No
Secondary Surgical details Operative duration,Fluoroscopy time,Blood loss, Blood transfusion,Any possible intraoperative complications Intraoperative Yes
Secondary Early postoperative complications Deep vein thrombosis (DVT), Skin necrosis, Infection, Loss of reduction, Arthritis,Death One month No
Secondary Late postoperative complications Heterotopic ossification, Chondrolysis, Avascular necrosis,Posttraumatic arthrosis One year No
Secondary Evaluation of Clinical outcome According to a modified Merle d'Aubigne and Postel score One year No
See also
  Status Clinical Trial Phase
Recruiting NCT05357079 - Impact of Topical Tranexamic Acid on Pre- and Post-operative Hemoglobin/Hematocrit Early Phase 1