The efficacy of the IDD-protocol with Accu-Spina for patients with low back pain

The efficacy of the IDD-protocol with Accu-Spina for patients with low back pain - Accu-Spina

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON30194

Enrollment

Registered

2006-11-17

Start date

2006-08-01

Completion date

Unknown

Last updated

2024-06-18

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

Conditions

backpain Low-Back Pain

Interventions

The intervention under investigation is the Accu-Spina treatment. The therapeutic effect of the Accu-Spina treatment is accomplished through distraction to the affected motion segment. The distracti

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: · Low back pain for more than 3 months · Bulging disc · Lumbar degenerative disc disease · Place of residence within 25 km from Nijmegen

Exclusion criteria

Exclusion criteria: · Previous surgical treatment with dynamic stabilisation, fusion or disc replacement · Radicular leg pain · Malignancy · Pregnancy · Osteoporosis · Refusal of the patient to participate (Dependend on requirement)

Design outcomes

Primary

Measure	Time frame
· VAS score for low back pain	—

Secondary

Measure	Time frame
· VAS score for leg pain · VAS score for satisfaction · Oswestry disability index · SF-36	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)