- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05171140
Influence of the Spatial Distribution of Hollow Screws on the Blood Supply and Prognosis of Femoral Neck Fractures
December 14, 2021 updated by: RenJi Hospital
Influence of Different Spatial Distribution of Hollow Screws on Blood Supply and Prognosis of Femoral Neck Fractures in the Elderly
Femoral neck fracture is a common type of fracture in the elderly.
For those without significant displacement (Garden I, II), more hip-preserving treatment strategies are adopted.
The classic parallel hollow screw internal fixation for hip-preserving treatment is based on the sliding compression theory, and a clinical debate has gradually emerged, that is, the positive triangle And the two different spatial distribution methods of hollow nails and inverted triangle, which one is better.
In addition, the distribution of hollow nails in actual operations is difficult to achieve a standard triangular distribution, and the damage to the epiphyseal vessels in the femoral head caused by repeated drilling of the guide needle cannot always be ignored.
The relationship between the distribution and injury of blood vessels in the femoral head and the spatial distribution of hollow screws on the prognosis of head necrosis of non-displaced femoral neck fractures in the elderly is worth studying.
This topic is based on the three advantages of TianJi orthopedic robots used in the elderly femoral neck fracture hollow nail hip-saving surgery: 1.standardized triangular nail placement with strong repeatability; 2. precise nail placement to reduce the risk of screw penetration; 3. limited guide pins The number of drill holes is to rule out repeated drill holes that damage the blood vessels in the femoral head.
The preoperative and postoperative vascular injury in the femoral head (enhanced MRI of the femoral head) was compared to assess the prognosis of patients, and to clarify the influence of the spatial distribution of hollow screws on the blood supply and prognosis of the femoral neck fracture in the elderly.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
the investigators choose 60-80-year-old Garden I or II patients with initial fractures.
Hollow nails are the first choice for treatment of these patients.
However, the spatial arrangement of hollow nails, local blood supply, and biomechanical properties have a greater impact on the prognosis of fractures.
, There are still some controversies, which are also the current research hotspots.
Our research conclusions may increase the success rate of hip preservation and will guide the treatment of these patients.
This study is based on the precise placement of nails by the Dimensity orthopedic robot, and compares the vascular injury of the femoral head before and after the nail placement (femoral head enhanced MRI) to assess the prognosis of the patient.
The influence of blood supply and prognosis of femoral neck fracture in the elderly.
Study Type
Interventional
Enrollment (Anticipated)
68
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
- Name: Ping Huang, Master
- Phone Number: +86 13916121692
- Email: 8813@renji.com
Study Locations
-
-
Shanghai
-
Shanghai, Shanghai, China, 200127
- Recruiting
- Renji hospital
-
Contact:
- Ping Huang
- Phone Number: +8613916121692
- Email: 8813@renji.com
-
-
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
56 years to 76 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- A new initial intracapsular fracture of the femoral neck;
- Garden classification I or II;
- Accept closed reduction robot-assisted hollow nail surgery;
- ASA score 1-2, can tolerate anesthesia;
- Age 60-80 years old (inclusive);
- Able to fully understand and voluntarily sign informed consent.
Exclusion Criteria:
- Old or pathological fractures;
- Patients with acetabular fracture;
- Those who have general conditions or accompanying diseases that make it difficult for people to tolerate surgery, such as: coagulation dysfunction, or heart, liver, and kidney dysfunction;
- Severe infections systemically or locally;
- Those who refuse to sign informed consent;
- In any case, if the researcher believes that the patient is not suitable for this treatment or there are other factors that affect the efficacy of the observation of this study.
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: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Hollow nails are arranged in a triangle
|
Triangular Nail Placement of Femoral Neck in arm A Femoral Neck Inverted Triangle Nail Surgery in arm B
|
|
Experimental: Hollow nail inverted triangle arrangement
|
Triangular Nail Placement of Femoral Neck in arm A Femoral Neck Inverted Triangle Nail Surgery in arm B
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
comparison of hip joint function at 6 months
Time Frame: 6 months after surgery
|
Harris score
|
6 months after surgery
|
|
comparison of hip joint function at 12 months
Time Frame: 12 months after surgery
|
Harris score
|
12 months after surgery
|
|
Imaging evaluation of the vascular condition of the femoral head epiphysis before surgery
Time Frame: One day before surgery
|
Imaging evaluation of the vascular condition of the femoral head epiphysis
|
One day before surgery
|
|
Imaging evaluation of the vascular condition of the femoral head epiphysis after surgery
Time Frame: 2 months after surgery
|
Imaging evaluation of the vascular condition of the femoral head epiphysis
|
2 months after surgery
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Intraoperative indicators-surgical blood loss
Time Frame: Intraoperative
|
surgical blood loss(ml)
|
Intraoperative
|
|
Intraoperative indicators-operation time
Time Frame: Intraoperative
|
operation time(minute)
|
Intraoperative
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Ping Huang, Master, Shanghai Jiaotong University School of Medical Renji Hospital
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)
September 1, 2020
Primary Completion (Anticipated)
January 31, 2023
Study Completion (Anticipated)
August 31, 2023
Study Registration Dates
First Submitted
November 22, 2021
First Submitted That Met QC Criteria
December 14, 2021
First Posted (Actual)
December 28, 2021
Study Record Updates
Last Update Posted (Actual)
December 28, 2021
Last Update Submitted That Met QC Criteria
December 14, 2021
Last Verified
November 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2020YJZX0112
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.