search
Back to results

A Modified Placement of Two Additional Pedicle Screws at the Fracture Level for the Treatment of Thoracolumbar Burst Fractures--a Study Protocol of a Randomised Controlled Trial

Primary Purpose

Posterior Short-segment Pedicle Instrumentation

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
fractured level screws-distraction
Sponsored by
Second Affiliated Hospital of Wenzhou Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Posterior Short-segment Pedicle Instrumentation

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria

  1. 18 years of age or above.
  2. single thoracolumbar burst fractures
  3. AO type A3 or A4 fractures
  4. Thoracolumbar Injury Classification and Severity Score (TLICS) of more than 4 and duration of < 2 weeks
  5. application of posterior short-segment pedicle screws instrumentation at the fracture level Exclusion criteria

1. previous pedicle instrumentation at the same level 2. multi-segmental thoracolumbar fractures or not AO type A3 or A4 are found 3. pregnancy 4. active infection or surgical site of the previous infection 5. planned emigration abroad within 2 years after inclusion 6. suffering from illness or long-term use of certain drugs affecting the stability of the spinal environment, such as metabolic bone disease, spinal tuberculosis and so on 7. the current use of anticoagulant (such as warfarin) or postoperative heparin for more than 6 months

Sites / Locations

  • The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Screw-Distraction (SD) group

Distraction-Screw (DS) group

Arm Description

six pedicle screws were implanted firstly, then distraction was achieved.

four pedicle screws were implanted firstly, then distraction was achieved, two additional screws were introduced at the fracture level at last.

Outcomes

Primary Outcome Measures

compression ratio change of anterior border of vertebral body height
using X-ray fluorescence
Depth of nail into injured vertebrae
using X-ray fluorescence
Kyphosis (Cobb) angle change
using X-ray fluorescence

Secondary Outcome Measures

Operative time
Unit of Measure is hour
intraoperative blood loss
Unit of Measure is ml
Complications
Pedicle fractures, intraoperative pars fractures, postoperative infection, deep venous thrombosis, nerve injury, and any other direct or indirect surgical complications will be recorded.
pain degree of back and lower limb
The pain degree of back and lower limb during follow-up will be assessed by the VAS of back pain and VAS of leg pain
Oswestry Disability Index (ODI) change
The Oswestry Disability Index (ODI) will be asssessed by questionnaire
The Japanese Orthopaedic Association (JOA) scores
Functional improvement is expressed by the rate of recovery of the JOA scores
The American Spinal Injury Association (ASIA) impairment scale
Spinal Injury was assessed using ASIA

Full Information

First Posted
December 5, 2017
Last Updated
August 26, 2018
Sponsor
Second Affiliated Hospital of Wenzhou Medical University
search

1. Study Identification

Unique Protocol Identification Number
NCT03384368
Brief Title
A Modified Placement of Two Additional Pedicle Screws at the Fracture Level for the Treatment of Thoracolumbar Burst Fractures--a Study Protocol of a Randomised Controlled Trial
Official Title
A Modified Placement of Two Additional Pedicle Screws at the Fracture Level for the Treatment of Thoracolumbar Burst Fractures--a Study Protocol of a Randomised Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2018
Overall Recruitment Status
Unknown status
Study Start Date
December 1, 2018 (Anticipated)
Primary Completion Date
December 30, 2019 (Anticipated)
Study Completion Date
December 30, 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Second Affiliated Hospital of Wenzhou Medical University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Controversies exist about the best treatment of burst fractures of the thoracolumbar spine. Adding screws in fractured segment has been proved in many literatures that can improve construct stiffness but sometimes aggravate the trauma of fractured vertebra. Therefore, we are eager to find an optimized placement of two additional pedicle screws at the fracture level for the treatment of thoracolumbar burst fractures. This is the first randomised controlled study investigating efficacy of diverse orders of pedicle screws placement and will provide recommendations for treating patients with thoracolumbar burst fractures.
Detailed Description
A blinded randomised controlled trial (blinding for the patient and statistician, rather than for the clinician and researcher) will be conducted. A total of seventy patients with single thoracolumbar AO type A3 or A4 fractures who are candidates for application of short-segment pedicle screws of fractured vertebrae will be randomly allocated to either the DS group (distraction-screws ) or the SD group (screws-distraction) at a ratio of 1: 1. The primary clinical outcome measures are compression ratio of anterior border of vertebral body height, depth of nail into injured vertebrae and kyphosis (Cobb) angle. Secondary clinical outcome measures are complications, Visual Analogue Scale (VAS) of back and leg pain, neurological function, operating time, intraoperative blood loss, Japanese Orthopaedic Association (JOA) scores and Oswestry Disability Index. These parameters will be evaluated preoperatively, intraoperatively, on day 3 postoperatively and then at 1, 3, 6, 12 and 24 months postoperatively.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Posterior Short-segment Pedicle Instrumentation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
70 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Screw-Distraction (SD) group
Arm Type
Placebo Comparator
Arm Description
six pedicle screws were implanted firstly, then distraction was achieved.
Arm Title
Distraction-Screw (DS) group
Arm Type
Experimental
Arm Description
four pedicle screws were implanted firstly, then distraction was achieved, two additional screws were introduced at the fracture level at last.
Intervention Type
Device
Intervention Name(s)
fractured level screws-distraction
Intervention Description
four pedicle screws were implanted into the upper vertebra and the lower vertebral body of the fractured vertebra. Then, immediate reduction and decompression were achieved by applying distraction of rod. Finally, two additional screws were introduced at fracture level
Primary Outcome Measure Information:
Title
compression ratio change of anterior border of vertebral body height
Description
using X-ray fluorescence
Time Frame
preoperatively, intraoperatively, on day 3 postoperatively and then at 1, 3, 6, 12 and 24 months postoperatively
Title
Depth of nail into injured vertebrae
Description
using X-ray fluorescence
Time Frame
at postoperation immediately
Title
Kyphosis (Cobb) angle change
Description
using X-ray fluorescence
Time Frame
preoperatively, intraoperatively, on day 3 postoperatively and then at 1, 3, 6, 12 and 24 months postoperatively
Secondary Outcome Measure Information:
Title
Operative time
Description
Unit of Measure is hour
Time Frame
right after surgery
Title
intraoperative blood loss
Description
Unit of Measure is ml
Time Frame
right after surgery
Title
Complications
Description
Pedicle fractures, intraoperative pars fractures, postoperative infection, deep venous thrombosis, nerve injury, and any other direct or indirect surgical complications will be recorded.
Time Frame
at postoperation immediately, 1, 3 and 6 months, and at 1 and 2 years postoperatively.
Title
pain degree of back and lower limb
Description
The pain degree of back and lower limb during follow-up will be assessed by the VAS of back pain and VAS of leg pain
Time Frame
preoperatively, on day 3 postoperatively and then at 1, 3, 6, 12 and 24 months postoperatively.
Title
Oswestry Disability Index (ODI) change
Description
The Oswestry Disability Index (ODI) will be asssessed by questionnaire
Time Frame
preoperatively, on day 3 postoperatively and then at 1, 3, 6, 12 and 24 months postoperatively
Title
The Japanese Orthopaedic Association (JOA) scores
Description
Functional improvement is expressed by the rate of recovery of the JOA scores
Time Frame
preoperatively and postoperatively including day 3 and then 1, 3, 6, 12 and 24 months
Title
The American Spinal Injury Association (ASIA) impairment scale
Description
Spinal Injury was assessed using ASIA
Time Frame
preoperatively, on day 3 postoperatively and then at 1, 3, 6, 12 and 24 months postoperatively

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria 18 years of age or above. single thoracolumbar burst fractures AO type A3 or A4 fractures Thoracolumbar Injury Classification and Severity Score (TLICS) of more than 4 and duration of < 2 weeks application of posterior short-segment pedicle screws instrumentation at the fracture level Exclusion criteria 1. previous pedicle instrumentation at the same level 2. multi-segmental thoracolumbar fractures or not AO type A3 or A4 are found 3. pregnancy 4. active infection or surgical site of the previous infection 5. planned emigration abroad within 2 years after inclusion 6. suffering from illness or long-term use of certain drugs affecting the stability of the spinal environment, such as metabolic bone disease, spinal tuberculosis and so on 7. the current use of anticoagulant (such as warfarin) or postoperative heparin for more than 6 months
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Wen-Fei Ni, Pro
Phone
86057788002814
Email
wenfeini@yeah.net
Facility Information:
Facility Name
The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University
City
Wenzhou
State/Province
Zhejiang
ZIP/Postal Code
325000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
WENFEI NI

12. IPD Sharing Statement

Citations:
PubMed Identifier
30696677
Citation
Hu ZC, Li XB, Feng ZH, Wang JQ, Gong LF, Xuan JW, Fu X, Jiang BJ, Wu L, Ni WF. Modified pedicle screw placement at the fracture level for treatment of thoracolumbar burst fractures: a study protocol of a randomised controlled trial. BMJ Open. 2019 Jan 28;9(1):e024110. doi: 10.1136/bmjopen-2018-024110.
Results Reference
derived

Learn more about this trial

A Modified Placement of Two Additional Pedicle Screws at the Fracture Level for the Treatment of Thoracolumbar Burst Fractures--a Study Protocol of a Randomised Controlled Trial

We'll reach out to this number within 24 hrs