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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03948542
Other study ID # F.o.t.H. Version 1.0
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2014
Est. completion date March 1, 2015

Study information

Verified date May 2019
Source Medical University of Vienna
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study addresses the question if patients with fractures of the humeral shaft and primary radial nerve palsy gain nerve recovery.

Additionally the influence of injury mechanism, fracture type, and treatment modality on nerve recovery should be evaluated.


Description:

Adult fractures of the humeral shaft account for approximately 3% of all fractures; most can be treated nonoperatively. Due to the anatomy of the radial nerve and the entrapment between fragments in spiral fractures of the humerus, these injuries are associated with primary radial nerve palsy in up to 18%.

Therefore, the purpose of this study was to assess the influence of injury mechanism, fracture type, and type of surgical treatment on time to onset of nerve recovery and time to full nerve recovery in patients with humeral shaft fractures and concomitant primary radial nerve palsy.

A retrospective analysis of prospectively collected data for all patients treated with humeral shaft fracture and primary radial nerve palsy at an academic Level-I trauma center was performed. Between 1994 and 2013 a total of 615 patients with traumatic humeral shaft fractures were treated at the department. The dataset was examined for completeness and accuracy. Patients with an incomplete dataset, those with a pathologic or periprosthetic fracture, patients with non-surgical treatment, or who were younger than 18 years of age were excluded from this series. According to these criteria, a total of 50 patients with a humeral shaft fracture and primary radial nerve underwent surgical treatment


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date March 1, 2015
Est. primary completion date January 1, 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- patients treated with humeral shaft fracture and primary radial nerve palsy between 1994 and 2013 at the Department of Trauma Surgery, Medical University of Vienna

- surgical treatment

- complete data sets

- minimum 18 years of age

Exclusion Criteria:

- Patients with an incomplete dataset

- those with a pathologic or periprosthetic fracture

- patients with non-surgical treatment

- or who were younger than 18 years of age

Study Design


Intervention

Other:
Outcome
Nerve Recovery NCV Funcional assessment

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Medical University of Vienna

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in nerve recovery; Nerve recovery after humeral shaft fracture and surgical treatment, Functional assessment Functional assessment was routinely performed at all follow up visits including a clinical evaluation and muscle strength (M0-M5) with a manual muscle test that was graded according to Daniels and Worthingham. through study completion, from date of inclusion till first documented changes in nerve recovery, from date of admission assessed up to 36 months
Secondary Nerve conduction studies (NCV) were performed routinely at two weeks following onset of radial nerve palsy and after 4 months in case of delayed recovery. Nerve conduction studies 2 weeks, 4 months
Secondary Radiographic examination via X-ray in two planes X-ray in two planes 3, 6 and 12 months after trauma
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