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

Phase 2

• Conditions: backpain; Low-Back Pain; 10023213; 10041543; 10009720

• Registration Number: NL-OMON30194
• Lead Sponsor: Sint Maartenskliniek

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 18 June 2024

Recruitment & Eligibility

• Status: Pending
• Sex: Not specified
• Target Recruitment: 60

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

· 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)

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>· VAS score for low back pain</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>· VAS score for leg pain<br /><br>· VAS score for satisfaction<br /><br>· Oswestry disability index<br /><br>· SF-36</p><br>