Effect of Topical Corticosteroids on Dysphagia in Anterior Cervical Discectomy and Fusion
Primary Purpose
Cervical Disc Herniation, Cervical Degenerative Disc Disease, Cervical Spondylotic Myelopathy
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Methylprednisolone Acetate
Hemostatic Matrix Kit
Sponsored by
About this trial
This is an interventional prevention trial for Cervical Disc Herniation focused on measuring Anterior Cervical Discectomy and Fusion, Dysphagia, ACDF
Eligibility Criteria
Inclusion Criteria:
- Any patient > 18 years undergoing a 2-4 level Anterior Cervical Discectomy and Fusion
Exclusion Criteria:
- Patients undergoing revision surgery
- Pediatric patients
- Trauma patients with cervical spine fractures
- Patients with cancer
- Patients with active infection
- Patients with a known allergy to Methylprednisolone Acetate
- Patients who refuse to participate
- Non English speakers
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Treatment
Control
Arm Description
Procedure: Anterior Cervical Discectomy and Fusion. The treatment arm will receive 40 mg of Methylprednisolone Acetate delivered with a Hemostatic Matrix Kit prior to closure.
Procedure: Anterior Cervical Discectomy and Fusion. The control group will receive only a Hemostatic Matrix Kit prior to closure.
Outcomes
Primary Outcome Measures
Degree of Dysphagia Patients Experience (Burden)
SWAL-QOL survey - Burden domain Score ranges between 0 and 100 (worst-best)
Degree of Dysphagia Patients Experience (Eating Desire)
SWAL-QOL survey - Eating desire domain Score ranges between 0 and 100 (worst-best)
Degree of Dysphagia Patients Experience (Eating Duration)
SWAL-QOL survey - Eating duration domain Score ranges between 0 and 100 (worst-best)
Degree of Dysphagia Patients Experience (Food Selection)
SWAL-QOL survey - Food Selection domain Score ranges between 0 and 100 (worst-best)
Degree of Dysphagia Patients Experience (Communication)
SWAL-QOL survey - Communication domain Score ranges between 0 and 100 (worst-best)
Degree of Dysphagia Patients Experience (Fear Swallow)
SWAL-QOL survey - Fear swallow domain Score ranges between 0 and 100 (worst-best)
Degree of Dysphagia Patients Experience (Social)
SWAL-QOL survey - Social domain Score ranges between 0 and 100 (worst-best)
Degree of Dysphagia Patients Experience (Mental)
SWAL-QOL survey - Mental domain Score ranges between 0 and 100 (worst-best)
Degree of Dysphagia Patients Experience (Sleep)
SWAL-QOL survey - Sleep domain Score ranges between 0 and 100 (worst-best)
Degree of Dysphagia Patients Experience (Fatigue)
SWAL-QOL survey - Fatigue domain Score ranges between 0 and 100 (worst-best)
Secondary Outcome Measures
Patient Reported Swallowing Difficulty Over 1 Year
The Eating Assessment Tool (EAT-10) is used to screen for self-perceived oropharyngeal dysphagia (OD) in community-dwelling elders. A summated EAT-10 total score ranges from 0 to 40, with a score ≥ 3 indicative of OD.
Modified Eat-10 : Eat-10 questionnaire without questions 1 ("My swallowing problem has caused me to lose weight") and 2 ("My swallowing problem interferes with my ability to go out for meals") to be applicable during hospitalization.
Eat-10 interpretation: Score ranging from 0 to 40 (best-worst)
each question response is 0-4, 0=no problem and 4=severe problem; score is a summation of each question's response Modified EAT-10 interpretation: Score ranging from 0 to 32 (best-worst)
each question response is 0-4, 0=no problem and 4=severe problem; score is a summation of each question's response
Patients' Bazaz Dysphagia Score - Liquid
Bazaz dysphagia scale defines dysphagia as none, mild, moderate and severe, depending on patients' symptoms with solid and liquid foods.
Patients' Bazaz Dysphagia Score - Solid
Bazaz dysphagia scale defines dysphagia as none, mild, moderate and severe, depending on patients' symptoms with solid and liquid foods.
Patients' Neck Disability
Neck Disability Index (NDI) Range from 0 to 100 (best-worst)
Patients' Pain Scores on the Visual Analog Scale - Neck Pain
Visual Analog Scale (VAS) - Neck pain Range from 0 to 100 (best-worst)
Patients' Pain Scores on the Visual Analog Scale - Left Arm Pain
Visual Analog Scale (VAS) - Left arm pain Range from 0 to 100 (best-worst)
Patients' Pain Scores on the Visual Analog Scale - Right Arm Pain
Visual Analog Scale (VAS) - Right arm pain Range from 0 to 100 (best-worst)
Change in Pre-vertebral Soft Tissue Swelling Over 1 Year
We are unable to report this outcome measure because soft tissue swelling was not assessed. The PI deemed it would not be included for this study as there is not a clinical or research standard to do so, nor is there normative data over time to compare against. Thus, data were not collected.
Fusion Rate
Flex-Ex X-rays
Bony bridging on a CT scan
Obvious bony remodeling on lateral X-ray
Adverse Event
Adverse Event (AE) following surgical treatment.
Adverse event were classified by severity based on the AO-ISSG criteria and treatment required:
Mild: Observed, medication, consult, X-ray. Essentially any management that was quick and easy and could be done at bedside Moderate: ICU admission, re-intubation, complication that had a documented prolonged hospital stay, medical procedure (such as flexible endoscopy), re-presentation to ED Severe: Inpatient re-admission, return to OR for any reason, mortality, failed OR.
AE were also categorize as Surgery-site related or unrelated adverse event. Finally, AE were also categorize as potentially related to steroid use (example: leukocytosis, pseudoarthrosis, or wound complications)
Full Information
NCT ID
NCT02539394
First Posted
August 27, 2015
Last Updated
June 16, 2023
Sponsor
Hospital for Special Surgery, New York
1. Study Identification
Unique Protocol Identification Number
NCT02539394
Brief Title
Effect of Topical Corticosteroids on Dysphagia in Anterior Cervical Discectomy and Fusion
Official Title
Do Intraoperative Topical Corticosteroids Aid in the Prevention of Postoperative Dysphagia Following Elective Anterior Cervical Discectomy and Fusion? A Randomized, Controlled, Double Blinded Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
June 2023
Overall Recruitment Status
Completed
Study Start Date
August 2015 (undefined)
Primary Completion Date
November 12, 2020 (Actual)
Study Completion Date
November 12, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital for Special Surgery, New York
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to determine what effect intraoperative topical steroids have on reducing swallowing difficulty following Anterior Cervical Discectomy and Fusion surgery.
Detailed Description
Background: Dysphagia is a serious post-operative concern in patients following anterior cervical surgery. Although many experts have acknowledged that dysphagia is often incompletely understood and defined, there is a significant amount of literature to support the significance of this clinical entity. This is the first randomized study to examine the use of topical steroids for the prevention of dysphagia postoperatively after anterior cervical discectomy and fusion.
Study Design: This study is a single site, double blinded randomized control trial. All individuals undergoing 2-4 level ACDF that meet the inclusion criteria will be randomized to either:
treatment arm or
control arm.
Both arms will undergo their planned surgeries and will receive the exact same procedure and standard of care as if they were not enrolled in a study. The only difference is that the treatment arm will receive 40 mg of Methylprednisolone Acetate delivered with one Hemostatic Matrix Kit injectable delivery vehicle prior to closure in the prevertebral soft tissues. The control group will receive only Hemostatic Matrix Kit prior to closure in the prevertebral soft tissues.
Outcomes: Patients will be asked to fill out questionnaires that assess dysphagia, general swallowing difficulty, and how neck pain impacts their quality of life. Additionally Radiographic images will be obtained at set time points to evaluate soft tissue inflammation and bony fusion.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cervical Disc Herniation, Cervical Degenerative Disc Disease, Cervical Spondylotic Myelopathy, Dysphagia, Osteoarthritis of Cervical Spine
Keywords
Anterior Cervical Discectomy and Fusion, Dysphagia, ACDF
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
128 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Treatment
Arm Type
Experimental
Arm Description
Procedure: Anterior Cervical Discectomy and Fusion. The treatment arm will receive 40 mg of Methylprednisolone Acetate delivered with a Hemostatic Matrix Kit prior to closure.
Arm Title
Control
Arm Type
Placebo Comparator
Arm Description
Procedure: Anterior Cervical Discectomy and Fusion. The control group will receive only a Hemostatic Matrix Kit prior to closure.
Intervention Type
Drug
Intervention Name(s)
Methylprednisolone Acetate
Other Intervention Name(s)
Depo-Medrol
Intervention Description
Methylprednisolone Acetate is a corticosteroid known to reduce swelling and inflammation.
Intervention Type
Other
Intervention Name(s)
Hemostatic Matrix Kit
Intervention Description
Hemostatic Matrix Kits help prevent uncontrollable bleeding in a operative site during a procedure.
Primary Outcome Measure Information:
Title
Degree of Dysphagia Patients Experience (Burden)
Description
SWAL-QOL survey - Burden domain Score ranges between 0 and 100 (worst-best)
Time Frame
Post-Op Day 1, Post-Op Day 2, Week 4-6, 3 Months, 6 Months, 12 Months
Title
Degree of Dysphagia Patients Experience (Eating Desire)
Description
SWAL-QOL survey - Eating desire domain Score ranges between 0 and 100 (worst-best)
Time Frame
Post-Op Day 1, Post-Op Day 2, Week 4-6, 3 Months, 6 Months, 12 Months
Title
Degree of Dysphagia Patients Experience (Eating Duration)
Description
SWAL-QOL survey - Eating duration domain Score ranges between 0 and 100 (worst-best)
Time Frame
Post-Op Day 1, Post-Op Day 2, Week 4-6, 3 Months, 6 Months, 12 Months
Title
Degree of Dysphagia Patients Experience (Food Selection)
Description
SWAL-QOL survey - Food Selection domain Score ranges between 0 and 100 (worst-best)
Time Frame
Post-Op Day 1, Post-Op Day 2, Week 4-6, 3 Months, 6 Months, 12 Months
Title
Degree of Dysphagia Patients Experience (Communication)
Description
SWAL-QOL survey - Communication domain Score ranges between 0 and 100 (worst-best)
Time Frame
Post-Op Day 1, Post-Op Day 2, Week 4-6, 3 Months, 6 Months, 12 Months
Title
Degree of Dysphagia Patients Experience (Fear Swallow)
Description
SWAL-QOL survey - Fear swallow domain Score ranges between 0 and 100 (worst-best)
Time Frame
Post-Op Day 1, Post-Op Day 2, Week 4-6, 3 Months, 6 Months, 12 Months
Title
Degree of Dysphagia Patients Experience (Social)
Description
SWAL-QOL survey - Social domain Score ranges between 0 and 100 (worst-best)
Time Frame
Post-Op Day 1, Post-Op Day 2, Week 4-6, 3 Months, 6 Months, 12 Months
Title
Degree of Dysphagia Patients Experience (Mental)
Description
SWAL-QOL survey - Mental domain Score ranges between 0 and 100 (worst-best)
Time Frame
Post-Op Day 1, Post-Op Day 2, Week 4-6, 3 Months, 6 Months, 12 Months
Title
Degree of Dysphagia Patients Experience (Sleep)
Description
SWAL-QOL survey - Sleep domain Score ranges between 0 and 100 (worst-best)
Time Frame
Post-Op Day 1, Post-Op Day 2, Week 4-6, 3 Months, 6 Months, 12 Months
Title
Degree of Dysphagia Patients Experience (Fatigue)
Description
SWAL-QOL survey - Fatigue domain Score ranges between 0 and 100 (worst-best)
Time Frame
Post-Op Day 1, Post-Op Day 2, Week 4-6, 3 Months, 6 Months, 12 Months
Secondary Outcome Measure Information:
Title
Patient Reported Swallowing Difficulty Over 1 Year
Description
The Eating Assessment Tool (EAT-10) is used to screen for self-perceived oropharyngeal dysphagia (OD) in community-dwelling elders. A summated EAT-10 total score ranges from 0 to 40, with a score ≥ 3 indicative of OD.
Modified Eat-10 : Eat-10 questionnaire without questions 1 ("My swallowing problem has caused me to lose weight") and 2 ("My swallowing problem interferes with my ability to go out for meals") to be applicable during hospitalization.
Eat-10 interpretation: Score ranging from 0 to 40 (best-worst)
each question response is 0-4, 0=no problem and 4=severe problem; score is a summation of each question's response Modified EAT-10 interpretation: Score ranging from 0 to 32 (best-worst)
each question response is 0-4, 0=no problem and 4=severe problem; score is a summation of each question's response
Time Frame
Pre-Op, Post-Op Day 1, Post-Op Day 2, Week 4-6, 3 Months, 6 Months, 12 Months
Title
Patients' Bazaz Dysphagia Score - Liquid
Description
Bazaz dysphagia scale defines dysphagia as none, mild, moderate and severe, depending on patients' symptoms with solid and liquid foods.
Time Frame
Pre-Op, Post-Op Day 1, Post-Op Day 2, Week 4-6, 3 Months, 6 Months, 12 Months
Title
Patients' Bazaz Dysphagia Score - Solid
Description
Bazaz dysphagia scale defines dysphagia as none, mild, moderate and severe, depending on patients' symptoms with solid and liquid foods.
Time Frame
Pre-Op, Post-Op Day 1, Post-Op Day 2, Week 4-6, 3 Months, 6 Months, 12 Months
Title
Patients' Neck Disability
Description
Neck Disability Index (NDI) Range from 0 to 100 (best-worst)
Time Frame
Pre-Op, Week 4-6, 3 Months, 6 Months, 12 Months
Title
Patients' Pain Scores on the Visual Analog Scale - Neck Pain
Description
Visual Analog Scale (VAS) - Neck pain Range from 0 to 100 (best-worst)
Time Frame
Pre-Op, Post-Op Day 1, Post-Op Day 2, Week 4-6, 3 Months, 6 Months, 12 Months
Title
Patients' Pain Scores on the Visual Analog Scale - Left Arm Pain
Description
Visual Analog Scale (VAS) - Left arm pain Range from 0 to 100 (best-worst)
Time Frame
Pre-Op, Post-Op Day 1, Post-Op Day 2, Week 4-6, 3 Months, 6 Months, 12 Months
Title
Patients' Pain Scores on the Visual Analog Scale - Right Arm Pain
Description
Visual Analog Scale (VAS) - Right arm pain Range from 0 to 100 (best-worst)
Time Frame
Pre-Op, Post-Op Day 1, Post-Op Day 2, Week 4-6, 3 Months, 6 Months, 12 Months
Title
Change in Pre-vertebral Soft Tissue Swelling Over 1 Year
Description
We are unable to report this outcome measure because soft tissue swelling was not assessed. The PI deemed it would not be included for this study as there is not a clinical or research standard to do so, nor is there normative data over time to compare against. Thus, data were not collected.
Time Frame
Pre-Op, Post-Op Day 1, Week 4-6, 3 Months, 6 Months, 12 Months
Title
Fusion Rate
Description
Flex-Ex X-rays
Bony bridging on a CT scan
Obvious bony remodeling on lateral X-ray
Time Frame
12 Months
Title
Adverse Event
Description
Adverse Event (AE) following surgical treatment.
Adverse event were classified by severity based on the AO-ISSG criteria and treatment required:
Mild: Observed, medication, consult, X-ray. Essentially any management that was quick and easy and could be done at bedside Moderate: ICU admission, re-intubation, complication that had a documented prolonged hospital stay, medical procedure (such as flexible endoscopy), re-presentation to ED Severe: Inpatient re-admission, return to OR for any reason, mortality, failed OR.
AE were also categorize as Surgery-site related or unrelated adverse event. Finally, AE were also categorize as potentially related to steroid use (example: leukocytosis, pseudoarthrosis, or wound complications)
Time Frame
12 month
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Any patient > 18 years undergoing a 2-4 level Anterior Cervical Discectomy and Fusion
Exclusion Criteria:
Patients undergoing revision surgery
Pediatric patients
Trauma patients with cervical spine fractures
Patients with cancer
Patients with active infection
Patients with a known allergy to Methylprednisolone Acetate
Patients who refuse to participate
Non English speakers
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Todd Albert, MD
Organizational Affiliation
Hospital for Special Surgery, New York
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Effect of Topical Corticosteroids on Dysphagia in Anterior Cervical Discectomy and Fusion
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