Surgical Treatment of Injuries and Consequences of the Acetabulum

August 15, 2023 updated by: Olzhas Bekarissov, National Scientific Center of Traumatology and Orthopedics named after academician N.D. Batpenov

Improving the Surgical Treatment of Injuries and Consequences of Injuries of the Acetabulum

The aim of the program is to develop technologies for the diagnosis and treatment of injuries and consequences of the pelvis.

Purpose: to improve the technique of surgical treatment of acetabular fractures.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

Tasks: Implementation of low-traumatic access to the acetabulum; introduction of a new implant for osteosynthesis of complex acetabular fractures into clinical practice; мathematical modeling of fixation of the acetabulum with a new implant; рublication of the results of the work carried out The relevance of the use of new implants in orthopedics is due to the problem of adaptation of implants in the body, especially with poor quality of bone tissue. Currently, work is underway to improve the materials and shapes of implants, new alloys are being studied, polymer implants are being introduced, but the problem of their integration into bones remains. A promising direction in orthopedics is the creation of implants as close as possible in their morphological shape and elasto-strength properties to human bone. But the creation of an absolute copy of the bone structure from a metal alloy leads to a weakening of its strength and loss of fixation stability, and subsequent lysis of the adjacent bone tissue.

All this indicates the need for further search for new, perhaps more promising and effective ways to solve this problem.

Study Type

Interventional

Enrollment (Estimated)

40

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

  • Kazakhstan
      • Astana, Kazakhstan, 010000
        • Recruiting
        • Center of National Scientific center Of Traumatology and Orthopedics named after academician N.D. Batpenov
        • Contact:
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • patients over 18 years of age
  • patients with acetabular fractures undergoing surgery
  • acetabular fractures according to the classification of Judet and Letournel

Exclusion Criteria:

  • patients under 18 years of age
  • posterior wall fracture according to the classification of Judet and Letournel

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Group A
Surgical intervention group
Procedure: Ostheosynthesis of acetabular fractures
The using of plate for fixation of acetabular fractures in surgical treatment

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
consolidation of fracture
Time Frame: 1 year follow-up
Evaluation of results using the radiological Matta criterion, the Harris Hip Score
1 year follow-up

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

National Scientific Center of Traumatology and Orthopedics named after academician N.D. Batpenov

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 25, 2021

Primary Completion (Estimated)

December 31, 2023

Study Completion (Estimated)

December 31, 2023

Study Registration Dates

First Submitted

August 15, 2023

First Submitted That Met QC Criteria

August 15, 2023

First Posted (Actual)

August 22, 2023

Study Record Updates

Last Update Posted (Actual)

August 22, 2023

Last Update Submitted That Met QC Criteria

August 15, 2023

Last Verified

August 1, 2023

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • BR11065157(04)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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