ClinicalTrials.gg
Not yet recruitingNCT06186362Updated Jan 5, 2024

Results of Distal Clavicle Graft in Shoulder Dislocation Clavicle Auto Graft in Patient With Recurrent Anterior Shoulder Dislocation

An observational study in Shoulder Injuries, sponsored by Al-Azhar University. Not yet recruiting. Open to participants aged 15 Years to 55 Years. Per ClinicalTrials.gov, last updated 2024-01-05.

Sponsored by Al-Azhar University · Observational

From the registry’s dates

  • Primary completion was expected by Jan 2025, 1 year 10 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
30
Ages
15 Years to 55 Years
Sex
All
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Study summary

to evaluate the clinical and radiological Outcome of Distal Clavicle Auto graft in patient with recurrent Shoulder dislocation

Read the detailed description

The glenohumeral joint is the most commonly dislocated joint of the human body,The stability of GH joint relies on a complex network of static and dynamic structures,The anterior labrum plays a key role in antero posterior stability as it deepens the glenoid cavity up to 50% There option for glenoid reconstruction including: Distal Clavicle Auto graft (DCA), proven is a good option to coracoid transfers

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Conditions studied

  • Shoulder Injuries

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03

In context

Shoulder Injuries

118 studies on the registry are indexed under Shoulder Injuries; 32 are open to participants now.

This study's planned enrollment of 30 is below the median of 60 across 45 observational studies indexed under Shoulder Injuries.

Browse Shoulder Injuries studies →

Lead sponsor

Al-Azhar University is the lead sponsor of 531 studies on the registry; 172 are open to participants now.

Of its 5 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

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

04

Who can participate

Ages eligible
15 Years to 55 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Range of motion "ROM" (Forward flexion, external rotation, internal rotation) Preoperative and postoperative ROM . Rowe score, Visual analogue score (VAS). Secondary outcomes postoperative complications will be evaluated.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Recurrent Traumatic anterior shoulder dislocation (≥ 3 times).

Exclusion criteria

Exclusion Criteria:

.On-track Hill-Sachs lesion. .Multi directional instability.

  • Voluntary dislocation.
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Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
30 participants (estimated)
Patient registry
No
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What researchers measure

Primary outcomes

  1. Row score

    Rang of motion

    Time frame: At 2 months, 6 months post operative

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Study locations

No study locations are listed for this record.

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References and documents

Publications

  • Kane P, Bifano SM, Dodson CC, Freedman KB. Approach to the treatment of primary anterior shoulder dislocation: A review. Phys Sportsmed. 2015 Feb;43(1):54-64. doi: 10.1080/00913847.2015.1001713. Epub 2015 Jan 6. PubMed 25559018 ↗
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Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Jan 2024; primary completion for Jan 2025, 12 months later.

Of 24 observational studies under Shoulder Injuries, half reached primary completion within 22 months of starting (the median), counting those still running; a quarter within 4 and three quarters within 45. This study's planned 12 months is below that.

How these figures are worked out, and which studies are left out of them.

Registered
Nov 20, 2023
First posted
Jan 2, 2024
StartEst.
Jan 2024
Primary completionEst.
Jan 2025
CompletionEst.
Jan 2025
Last update
Jan 5, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jan 5, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06186362
Responsible party
Mostafa Khalaf Mahmoud Mohammed (Principle investigator, Al-Azhar University) — Principal investigator
First posted
Jan 2, 2024
Start date
Jan 2024 (estimated)
Primary completion
Jan 2025 (estimated)
Completion
Jan 2025 (estimated)
Last update
Jan 5, 2024

Study contacts

Hosam Elsayed Abd-Elzaher, Lecturer
Contact
Hosamortho@gmail.com
+201008832805
Mohammed Mousa Mohammed, Assistant Professor
Contact
MohamedMahmoud.2244@azhar.edu.eg
+201009092327

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Dec 2023. You cannot join it, but the record below documents what was studied.

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