Viewing Study NCT00415220



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Study NCT ID: NCT00415220
Status: COMPLETED
Last Update Posted: 2006-12-22
First Post: 2006-12-21

Brief Title: Manipulation or Microdiscectomy For Sciatica A Prospective Randomized Controlled Trial
Sponsor: McMorland Gordon DC
Organization: McMorland Gordon DC

Study Overview

Official Title: Comparison of Treatment Outcomes Between Chiropractic and Back Surgery for the Treatment of Sciatica Secondary to Lumbar Herniated Disc A Prospective Randomized Controlled Trial
Status: COMPLETED
Status Verified Date: 2006-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study was to compare standardized chiropractic treatment spinal manipulation to back surgery microdiscectomy for patients with sciatica secondary to lumbar herniated disc refractory to medical management
Detailed Description: Context Operative management of lumbar radiculopathy caused by lumbar disc herniation LDH in patients refractory to medical management provides rapid and effective symptom relief However both short and long term benefits of surgery continue to be scrutinized

Objective To compare clinical efficacy of Chiropractic Treatment against Microdiscectomy in patients suffering from sciatica secondary to LDH

Study Design Prospective Randomized Controlled Clinical Trial allowing crossover recruitment 2000-2004 1 year follow-up

Setting Elective primary care physician referrals made directly to neurosurgical spine surgeons at the Foothills Hospital and Medical Centre University of Calgary

Patients Forty consecutive consenting patients with sciatica from LDH refractory to at least three months of non-operative care and found appropriate for surgery

Interventions Surgical microdiscectomy or standardized chiropractic treatment Crossover to the alternate treatment allowed after 3 months

Main Outcome Measures McGill Pain Score Roland Morris Disability Index Aberdeen Pain Scale and SF-36 General Health Survey before treatment initiation and after 3 6 12 24 and 52 weeks

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None