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Obstetrical brachial plexus lesion: a pilot study of outcome and general functioning in adults.

Obstetrical brachial plexus lesion: a pilot study of outcome and general functioning in adults. - OBPL: a pilot study of outcome and general functioning in adults.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON36402
Enrollment
30
Registered
2011-06-24
Start date
2012-02-03
Completion date
Unknown
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

erb's palsy obstetrical brachial plexus lesion

Interventions

None listed

Sponsors

Vrije Universiteit Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: The inclusion criteria are adults with unilateral OPBL, aged 18-65 years, able to speak Dutch or English.

Exclusion criteria

Exclusion criteria: The exclusion criteria are double sided OPBL and central neurological comorbidity.

Design outcomes

Primary

MeasureTime frame
DASH

Secondary

MeasureTime frame
X-ray anterioposterior and axial; right and left shoulder Passive range of motion test of the upper extremity Active range of motion test of the upper extremity Handheld dynomometry / Yamar dynamometer sensitivity 2-pointdiscrimination Scoliosis investagion (sitting) Armlength left and right (cm) Circumference of the arm, left and right (cm) VAS scores Modified Mallet-score ARA-test NHP-test MOS-SF 36

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)