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Posture control after lumbar microdiscectomy

Posture control after lumbar microdiscectomy: effect of transmuscular surgical approach and of early postoperative physiotherapy - a randomised clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN14206374
Enrollment
100
Registered
2008-03-10
Start date
2008-02-18
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Sciatica caused by a lumbar disc herniation Musculoskeletal Diseases Other intervertebral disc disorders

Interventions

1. Transmuscular surgical approach versus classic paramedian approach to the disc herniation at surgery 2. Early postoperative physiotherapy, starting two weeks postoperatively, and consisting of an i

Sponsors

University Hospitals Leuven (The Netherlands)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. One level disc herniation, either L4-L5 or L5-S1, explaining symptoms and representing operative indication. Purely median disc herniations are excluded. 2. Age: 18 - 60 years, either sex 3. Living within 30 km perimeter of the hospital 4. Informed consent signed

Exclusion criteria

Exclusion criteria: 1. Emergency operation required 2. Litigation, worker's compensation 3. Clinical suspicion of depression or fibromyalgia (the suffering is not exlusively explained by the disc herniation) 4. Previous lumbar surgery, irrespective of the level 5. Significant neurological deficit (weakness worse than 4/5) 6. Systemic disease significantly affecting patient's functioning (American Society of Anaesthesiologists [ASA] grade greater than 3) 7. Median disc herniation 8. Patient unable to communicate in the Dutch language

Design outcomes

Primary

MeasureTime frame
Muscle control (assessed by postural balance test and sit-to-stand test), assessed in the lab at two weeks, eight weeks and six months post-operatively.

Secondary

MeasureTime frame
Comfort: 1. Back pain 2. Sciatica 3. Functional status 4. Return to work Secondary outcome measures are assessed by standardised patient questionnaires preoperatively and at two weeks, eight weeks, six months and one year postoperatively.

Countries

Belgium

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026