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Lumbar microdiscectomy and post-operative activity restrictions

Impact of post-operative activity restrictions on lumbar microdiscectomy clinical outcome: a single blinded randomized controlled trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12616001360404
Enrollment
210
Registered
2016-09-30
Start date
2016-02-29
Completion date
2022-11-21
Last updated
2026-04-27

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

Conditions

None listed

Brief summary

Lumbar discectomy is the most commonly performed spine surgical procedure. Lumbar discectomy is performed to treat radicular pain (pain radiating along the distribution of a nerve) unresponsive to conservative management, neurological deficit or less commonly cauda equina syndrome. Lumbar discectomy has evolved to a relatively minimally invasive surgical procedure performed as a day procedure in many centres in North America. Traditionally surgeons have advised patients to restrict post-operative activity due to the hypothesis that this may reduce the risk of disc reherniation and progressive instability at the operated level. In contemporary practice many surgeons do not advise any post-operative activity restriction. Observational studies conducted to date investigating the effect of removal of activity restrictions demonstrated similar outcomes to those reported in the literature for traditional post-operative care. No randomized controlled trial has been performed to investigate this question. The purpose of this study is to directly compare in a randomized controlled trial patients following post-operative activity restrictions and those without post-operative activity restrictions for a period of one month following lumbar microdiscectomy. Patients will undergo standard lumbar microdiscectomy and then be randomized into either the treatment (no restrictions) or control (restrictions groups). For a period of one month following their procedure patients will wear an electronic monitoring device that will record activity and posture. Patients will complete surveys pre-operatively and post-operatively at day one, one month, three months, six months and twelve months. Patients will also undergo clinical review at one month following their operation. The primary endpoint is a composite endpoint of change in visual analogue scale for pain (for back and legs), Oswestry Disability Index, absence of disc herniation recurrence or reintervention at six months. Additional secondary endpoints will also be assessed.

Interventions

The trial investigates post-operative activity restrictions following lumbar discectomy. Patients are randomized prior to lumbar microdiscectomy surgery at L3/4, L4/5 or L5/S1 intervertebral discs to receive either the intervention (no post-operative activity restrictions for a period of one month following the procedure) or control group (traditional post-operative activity restrictions- defined below). The lumbar microdiscectomy operation is performed by Consultant Neurosurgeons or under the

The trial investigates post-operative activity restrictions following lumbar discectomy. Patients are randomized prior to lumbar microdiscectomy surgery at L3/4, L4/5 or L5/S1 intervertebral discs to receive either the intervention (no post-operative activity restrictions for a period of one month following the procedure) or control group (traditional post-operative activity restrictions- defined below). The lumbar microdiscectomy operation is performed by Consultant Neurosurgeons or under the supervision of Consultant Neurosurgeons in participating hospitals in Melbourne. Intervention group patients are advised by neurosurgical ward physiotherapists post-operatively to return to all activities as soon as they feel ready with no restrictions placed on sitting, exercise, return to work or sexual activity. The same information is communicated in an information sheet provided to patients. Patients wear a portable electronic device for a period of one month following their procedure which records activity and position: lying, sitting, standing, walking, running or cycling.

Sponsors

Assoc. Prof. Tony Goldschlager
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. Suffering from radiculopathy or radicular pain with concordant MRI evidence of lumbar disc herniation at L3/4, L4/5 or L5/S1 2. Deemed appropriate and booked for lumbar microdiscectomy by the treating clinician 3. Who agree to routine follow-up examination at 1 month, 3 months and 6 months 4. Who agree to wear a small electronic device to monitor position over a period of one month 5. Age 18 to 75

Exclusion criteria

1. Previous history of lumbar surgery, spinal infection or fracture.

Outcome results

None listed

Source: ANZCTR · Data processed: May 1, 2026