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Study on Outcomes of Proximal Humerus Fractures

U

University of Massachusetts, Worcester

Status

Begins enrollment in 6 months

Conditions

Proximal Humerus Fracture

Treatments

Procedure: open reduction internal fixation
Procedure: intramedullary nail
Procedure: reverse total shoulder arthroplasty

Study type

Interventional

Funder types

Other

Identifiers

NCT07060664
00002567

Details and patient eligibility

About

Patients undergoing either operative or non-operative treatment of proximal humerus fractures will be studied with the goal of understanding which treatment modality provides optimal post-injury outcomes.

Enrollment

100 estimated patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • individuals 65 years of age or older with proximal humerus fractures

Exclusion criteria

-

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

100 participants in 2 patient groups

Operative Management
Active Comparator group
Treatment:
Procedure: reverse total shoulder arthroplasty
Procedure: intramedullary nail
Procedure: open reduction internal fixation
Non-operative Management
No Intervention group

Trial contacts and locations

1

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Central trial contact

Gregory Iovanel, MD

Data sourced from clinicaltrials.gov

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