"Suture of the Tuberosities in Inverted Prostheses" Implanted for Acute Fractures of the Proximal Humerus?.

Sponsor
Hospital del Mar (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05462691
Collaborator
(none)
90
2
36

Study Details

Study Description

Brief Summary

Complex fractures of the proximal humerus in elderly patients constitute a growing problem. Osteoporosis linked to these fractures prevents osteosynthesis correctly, so that if the offset between the fragments is large, it is necessary to implant a prosthesis. Inverted prostheses, normally used for the treatment of osteoarthritis with absence of the rotator cuff, have become the treatment of choice in these fractures obtaining very favorable results. Traditionally, once the prosthesis is implanted, they are sutured the tuberosities with the rotator cuff tendons to the prosthesis. This gesture is supposed to will improve patient function. However, this prosthesis was originally designed for use in patients without a rotator cuff, so the need for this suture, which lengthens surgical time and requires an increase in the number of sutures, which can potentially increase the risk of infection. With the results of this study, it would be possible to reduce the surgical time, the number of inert materials implanted, and potentially the risk of infection.

Condition or Disease Intervention/Treatment Phase
  • Procedure: tuberosity suture
N/A

Detailed Description

Complex fractures of the proximal humerus in elderly patients constitute a growing problem. Osteoporosis linked to these fractures prevents osteosynthesis correctly, so that if the offset between the fragments is large, it is necessary to implant a prosthesis. Inverted prostheses, normally used for the treatment of osteoarthritis with absence of the rotator cuff, have become the treatment of choice in these fractures obtaining very favorable results. Traditionally, once the prosthesis is implanted, they are sutured the tuberosities with the rotator cuff tendons to the prosthesis. This gesture is supposed to will improve patient function. However, this prosthesis was originally designed for use in patients without a rotator cuff, so the need for this suture, which lengthens surgical time and requires an increase in the number of sutures, which can potentially increase the risk of infection. With the results of this study, it would be possible to reduce the surgical time, the number of inert materials implanted, and potentially the risk of infection.

Primary objective:

To determine if there are differences in the perception of quality of life measured by through the Simple Shoulder Test scale, among the patients in whom sutured the tuberosities and patients who have had the tuberosities excised tuberosities.

Secondary objectives:

To determine if there are differences between the patients in whom suturing has been the tuberosities and patients who have had their tuberosities excised about:

  • SPADI quality of life test.

  • Constant functional test.

  • number of prosthetic dislocations

  • Percentage of scapular notch development measured according to the Sirveaux scale.

  • Number of dislocations.

  • number of infections.

  • number of revision surgeries.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
90 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
prospective randomized trialprospective randomized trial
Masking:
Double (Participant, Outcomes Assessor)
Masking Description:
patients will be blinded to the assignment group. outcomes assessors will be blinded to the assignment group
Primary Purpose:
Treatment
Official Title:
"It is Necessary to Suture the Tuberosities in Inverted Prostheses Implanted for Acute Fractures of the Proximal Humerus?. Prospective Randomized Study
Anticipated Study Start Date :
Sep 1, 2022
Anticipated Primary Completion Date :
Sep 1, 2023
Anticipated Study Completion Date :
Sep 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Patients without tuberosity reconstruction

patients undergoing reverse shoulder arthroplasty because a proximal humeral fracture with suturing of the tuberosities

Procedure: tuberosity suture
to suture or not suture the tuberosities in reverse shoulder arthroplasty because of a proximal humeral fracture

Active Comparator: Patients with tuberosity reconstruction

patients undergoing reverse shoulder arthroplasty because a proximal humeral fracture without suturing of the tuberosities

Procedure: tuberosity suture
to suture or not suture the tuberosities in reverse shoulder arthroplasty because of a proximal humeral fracture

Outcome Measures

Primary Outcome Measures

  1. Simple Shoulder Test [24 months]

    Primary objective: To determine if there are differences in the perception of quality of life measured by through the Simple Shoulder Test scale, among the patients in whom sutured the tuberosities and patients who have had the tuberosities excised tuberosities.

Eligibility Criteria

Criteria

Ages Eligible for Study:
65 Years to 85 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • patients > 65 yrs. and < 85 yrs.

  • Acute fracture of the proximal humerus.

  • implantation of inverted shoulder prosthesis.

Exclusion Criteria:
  • acute fractures of more than 3 weeks of evolution

  • Associated fractures.

  • senile dementia and/or cognitive alterations that prevent compliance protocols

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Hospital del Mar

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Carlos Torrens, Clinical Professor, Hospital del Mar
ClinicalTrials.gov Identifier:
NCT05462691
Other Study ID Numbers:
  • 2022/10519
First Posted:
Jul 18, 2022
Last Update Posted:
Jul 18, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 18, 2022