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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04112485
Other study ID # HMU/Sherwan3
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 4, 2015
Est. completion date August 20, 2019

Study information

Verified date May 2020
Source Hawler Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

60 patients involved were divided into two matched groups; Group A: 30 patients were treated with conventional fenestration laminectomy and discectomy and Group B: 30 patients were treated with microdiscectomy. The age of the patients involved in this study ranged from 19 years old to 46 years old


Description:

60 patients involved were divided into two matched groups; Group A: 30 patients were treated with conventional fenestration laminectomy and discectomy and Group B: 30 patients were treated with microdiscectomy. The age of the patients involved in this study ranged from 19 years old to 46 years old. All the patient was suffering from symptomatic lumbar disc herniation L4-5. Each patient was assessed clinically and MRI was done for all the patients to prove clinically, the symptomatic lumbar disc herniation which was present in all patients.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date August 20, 2019
Est. primary completion date August 15, 2019
Accepts healthy volunteers No
Gender All
Age group 19 Years to 46 Years
Eligibility Inclusion Criteria:

- Adults who are symptomatic lumbar disc herniation L4-5. Each patient was assessed clinically and MRI was done for all the patients to prove clinically, the symptomatic lumbar disc herniation which was present in all patients. Conservative treatment for 6weeks was failed

Exclusion Criteria:

- smoking, previous lumbar spine surgery, Diabetes Melitus (DM) and neuromuscular disorders.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Microdiscectomy


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Hawler Medical University

Outcome

Type Measure Description Time frame Safety issue
Primary Visual analogue score Visual analogue score of back pain and leg pain which represent a score from 0-10 so if patient has no pain so gives 0 and if has severe pain gives 10 Visua analogue score was assessed preoperatively and postoperatively to see how much change in pain can occurred after open discectomy and after Microdiscectomy for 1 year
Primary Oswestry disability index Oswestry disability index in a measurement of functional ability of patients regarding pain and daily activities Oswestry disability index was assessed preoperatively and postoperatively to assess how much changes can occur after open discectomy and Microdiscectomy for 1 year after surgery
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