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Active, not recruitingNCT07257081BUTEE2024Updated Dec 17, 2025

Effect of Combining a Posterosuperior Humeral Notch Filling With a Coracoid Bone Block on the Rate of Return to Sport

An interventional study of Filling of the posterior superior notch of the humerus in Shoulder Injuries, sponsored by Clinique Saint Jean, France. Active, not recruiting at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-12-17.

Sponsored by Clinique Saint Jean, France · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Jul 2026, 3 months ago, but the record still lists the study as active, not recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
120
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The goal of this interventional study is to demonstrate the benefit of combining filling of the posterosuperior notch of the humerus with a coracoid stop on the rate of return to sports at the same level as before at 12 months post-surgery.

The level of sport will be categorized as recreational, competitive, or professional.

This is a prospective, single-center, comparative study of two parallel randomized groups, using a single-blind design.

The patients included will be randomized into two groups with a 1:1 ratio: one group will undergo the filling technique, while the second group will not. The rest of the surgery will be similar.

Randomization will be stratified according to initial athletic level.

02

Conditions studied

  • Shoulder Injuries

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03

In context

Shoulder Injuries

114 studies on the registry are indexed under Shoulder Injuries; 31 are open to participants now.

This study's planned enrollment of 120 is above the median of 55 across 65 interventional studies indexed under Shoulder Injuries.

Browse Shoulder Injuries studies →

Lead sponsor

Clinique Saint Jean, France is the lead sponsor of 15 studies on the registry; 6 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Adult patient affiliated with or entitled to social security coverage
  • Patient who has received informed consent about the study and signed a consent form
  • Patient presenting with previous shoulder instability associated with a compromising humeral lesion determined by CT scan measurement

Exclusion criteria

Exclusion Criteria:

  • Patient non-compliant with follow-up over 1 year
  • Recurrence of a previously operated shoulder
  • Patient under judicial protection, guardianship, or trusteeship.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
120 participants (estimated)

Study arms

  • No intervention
    Arthroscopic coracoid process resection

    Arthroscopic coracoid process resection

  • Experimental
    Arthroscopic coracoid process resection + filling of the posterosuperior notch of the humerus

    Arthroscopic coracoid process resection with filling of the posterosuperior notch of the humerus

    Procedure: Filling of the posterior superior notch of the humerus

Interventions

  • ProcedureFilling of the posterior superior notch of the humerus

    The intervention involves bringing part of the coracoid bone with the tendon attached to it onto the front of the glenoid cavity. The stop is secured with an endobutton. The additional procedure used in this study is filling the posterosuperior notch of the humerus. The filling technique involves placing two anchors, which causes tenodesis of the infraspinatus in the posterosuperior notch of the humerus.

06

What researchers measure

Primary outcomes

  1. Number of Participants returning to sports at the same level after surgery, in each arms, at 12months

    Difference between the two arms for returning to sports at the same level as before, categorized into three levels: recreational, competitive, or professional, 12 months after surgery.

    Time frame: 12 months

07

Study locations

1 site
  • Clinique St Jean Sud de France
    Saint-Jean-de-Védas, 34430, France
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 17, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07257081
Lead sponsor
Clinique Saint Jean, France
Responsible party
Sponsor
First posted
Dec 2, 2025
Start date
Nov 1, 2025
Primary completion
Jul 1, 2026 (estimated)
Completion
Jul 31, 2027 (estimated)
Last update
Dec 17, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Nov 2025. You cannot join it, but the record below documents what was studied.

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