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Short Versus Long Post-Operative Restrictions Following Lumbar Discectomy

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Mass General Brigham

Status

Unknown

Conditions

Lumbar Disc Herniation

Treatments

Behavioral: Two-Week Post-Operative Restriction
Behavioral: Six-Week Post-Operative Restriction

Study type

Interventional

Funder types

Other

Identifiers

NCT01363830
2009P001125

Details and patient eligibility

About

Post-operative restrictions following lumbar discectomy is a controversial topic. While the most widely accepted protocol restricts bending, lifting, and twisting for four to six weeks following discectomy, a number of studies support an early return to full activity without restriction. Since the goal of discectomy is to promptly provide pain relief and a return to a fully active lifestyle, perhaps post-operative restrictions are more hindering than beneficial.

Hypothesis: Post-operative restrictions following lumbar discectomy do not influence reherniation rate.

Specific Aim 1: To compare the reherniation rates between the 6-weeks of restriction and the 2-weeks of restriction groups.

Specific Aim 2: To determine the return to full activity and return to work dates of both the 6-weeks of restriction and 2-weeks of restriction groups.

Specific Aim 3: To assess the health outcomes of both the 6-weeks of restriction and 2-weeks of restriction groups.

Full description

Upon enrollment, subjects will be randomized to the "6-weeks of restriction" or "2-weeks of restriction" group. Subjects will also be asked to provide/complete:

  • demographical information
  • VAS back and leg score
  • Modified Oswestry questionnaire

All of the surgeries will be performed using a so-called limited discectomy in which the herniated disc fragment is removed without an aggressive disc space curettage. Prior to surgery, the subjects' discs will be classified by the Primary Investigator and Site Responsible Investigator on a T-2 weighted MRI according to the Carragee Disc Herniation Classification system.

The discs will be reassessed intraoperatively by the surgeon to confirm the assigned classification. In addition, a radiologist will review a random sampling set of discs on T-2 weighted MRI to eliminate bias and validate the classifications.

Subjects will be followed for a 2 year time period with study visits at 2 weeks, 6 weeks, 3 months, 1 year, and 2 years. At every follow-up visit, the following will be completed and/or documented:

  • A reherniation (any clinical symptoms of a reherniation will be verified and documented by MRI)
  • Return to full activity and/or work (date)
  • VAS back and leg score
  • Modified Oswestry questionnaire

Enrollment

420 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 years of age or older
  • English speaking
  • single level lumbar disc herniation
  • surgical candidate
  • no previous lumbar surgery
  • primary radicular pain

Exclusion criteria

  • Less than 18 years of age
  • Non-English speaking
  • Multi-level lumbar disc herniation
  • Disc reherniation
  • Previous lumbar surgery
  • Primary low back pain

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

420 participants in 2 patient groups

Two-Week Post-Operative Restriction
Experimental group
Description:
Restrict bending, lifting, and twisting for two-weeks following discectomy.
Treatment:
Behavioral: Two-Week Post-Operative Restriction
Six-Week Post-Operative Restriction
Active Comparator group
Description:
Restrict bending, lifting, and twisting for six-weeks following discectomy.
Treatment:
Behavioral: Six-Week Post-Operative Restriction

Trial contacts and locations

3

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Central trial contact

Christopher M Bono, M.D.; Dana A Leonard

Data sourced from clinicaltrials.gov

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