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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00444405
Other study ID # SJCNS-01
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date March 2007
Est. completion date April 2009

Study information

Verified date February 2020
Source Mercy Research
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to compare patients who underwent decompression/discectomy with pedicle screw fusion to patients who received decompression/discectomy without fusion.


Description:

Lumbar disc herniations are quite common and typically improve after surgical correction. However, some patients develop recurrent herniations at the same level. Controversy exists as to why reherniated discs occur. Moreover, existing research does not settle the issue of whether a second decompression/discectomy or a repeat decompression/discectomy with pedicle screw fusion is the more successful treatment. This study is designed to compare differences in patient-reported pain, physical function, and satisfaction between the two types of surgery patients.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date April 2009
Est. primary completion date April 2009
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- Recurrent lumbar disc herniation by MRI or CT with history of decompression at the same level in the past

- Recurrent symptomatic history (with or without back pain) with radicular leg pain that improved following the first surgery

- Male or female 18-75 years old

- Flexion and extension x-rays that demonstrate an absence of sponylolisthesis or spondylolisthesis with less than 3 mm of movement

Exclusion Criteria:

- Recurrence of disc herniation within 3 months of first decompression

- Multiple level herniated discs

- No history of lumbar back surgery except as in Inclusion criteria above

- Documented severe osteoporosis or osteopenia

- Symptoms of low back pain only

- Diabetes mellitus

- Patients with suspected or diagnosed psychological/psychiatric problems that could compromise the reliability of their results

- Lumbar spondylolisthesis on flexion/extension x-rays > 3 mm

- History of lumbar spine fractures (new or old)

- Any concurrent medical condition that may interfere with the interpretation of efficacy and safety data during the study

- Autoimmune diseases

- Age less than 18 or greater than 75 years

Study Design


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Mercy Research
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