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NCT03271060 Clinical Trial

Comparative Study Between Posterior Lumbar Interbody Fusion(PLIF) and Intertransverse Process Fusion in Treatment of Spodylolithesis

Lumbar Spondylolisthesis Clinical Trial

Official title:
Comparative Study Between Posterior Lumbar Interbody Fusion(PLF) and Intertransverse Process Fusion in Treatment of Spodylolithesis

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT03271060
Other study ID # Lumbar spondylolisthesis
Secondary ID
Status Not yet recruiting
Phase N/A
First received August 31, 2017
Last updated August 31, 2017
Start date September 1, 2017
Est. completion date September 1, 2019

Study information
Verified date August 2017
Source Assiut University
Contact Mahmoud Garamoun, Resident
Phone 201091123869
Email Garamoun.mahmoud@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The first technique described for interbody fusion was the anterior lumbar interbody fusion (ALIF).(20) For this technique, the intervertebral disc is accessed through a retroperitoneal or transperitoneal approach.

While the posterior approach was first described by Russell Hibbs in 1911, in the 1950's, Cloward (7)popularized the posterior approach for a posterior lumbar interbody fusion (PLIF).

Description:

In this study we will try to identify the benefits and outcome of posterior lumbar interbody fusion and inter transverse process bone graft fusion.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 30
Est. completion date September 1, 2019
Est. primary completion date August 30, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- lumbar spondylolisthesis

Exclusion Criteria:

- infection of lumbar spine

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Posterior lumbar interbody fusion
Lumbar fusion by screws and inter vertebral cage
• Inter transverse bone grafting
Inter transverse process bone grafting by bone graft from illiac crest or other sites

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Assiut University

Outcome
Type Measure Description Time frame Safety issue
Primary Back pain Back pain severity grading mild, moderate, severe 1year postoperative
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