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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05638074
Other study ID # 04.11.2022.1506
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date November 28, 2022
Est. completion date August 30, 2023

Study information

Verified date November 2022
Source Marmara University
Contact janbubi jandaulyet, residency
Phone +905076755161
Email janbubi.jandaulyet@marmara.edu.tr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Facet joints are synovial joints located on the dorsolateral side of the vertebral column. Normally, both facet joints are symmetrical. Facet tropism (FT) is defined as asymmetry between the angles of orientation of the joints, in which a facet joint in the same segment is more sagittally oriented than the other. In 1967, Farfan and Sullivan first reported that FT is a possible risk factor for the development of disk herniation. However, this is controversial as there are other views advocating that FT is not a risk factor for the development of cervical disc herniation. Further, it has been emphasized that patients with FT have a greater need for adjacent segment degeneration and new spinal surgery after spinal fusion surgeries than those without FT. In the current literature, studies have been conducted to examine the clinical and radiological parameters that may be related to the effectiveness of cervical interlaminar epidural steroid injections (ILESI). The aim of this study was to examine the effect of the presence of FT on ILESI results in patients with cervical disc herniation-induced radicular pain.


Recruitment information / eligibility

Status Recruiting
Enrollment 90
Est. completion date August 30, 2023
Est. primary completion date May 30, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: aged 18-75 years, who applied to the pain medicine outpatient clinic, had axial neck and unilateral radicular extremity pain for at least 3 months, and were diagnosed with protruded disc herniation by magnetic resonance imaging were included in the study Exclusion Criteria: Patients with systemic inflammatory disease, bleeding diathesis,history of psychiatric illness, malignancy, contrast material or local anesthetic agent allergy, cervical spinal stenosis, history of cervical ESI, or neck surgery in the last 3 months were excluded from the study

Study Design


Intervention

Procedure:
Interlaminar Epidural Steroid Injection
The patient will be placed in the prone position and cutaneous anesthesia is performed with 3 mL of 2% prilocaine using the sterile technique. After imaging the C7-T1 space with fluoroscopy, it will be entered from the right/left paramedian part of the C7-T1 space with an 18G Touhy needle, and the C-arm will be set in the contralateral oblique position for depth determination. Under intermittent fluoroscopic imaging, the needle will be advanced, and access to the epidural space wiil be confirmed by the loss of resistance technique. Afterwards, the epidural spread will be controlled with a contrast agent, and a mixture of 10 mg dexamethasone, 1 mL 2% lidocaine hydrochloride, and 1 mL 0.9% saline will be applied to the epidural space. The patient will be discharged with recommendations after being kept under observation for 2 hours post-procedure. All injections will be performed by the same pain medicine specialist who has at least 5 years of experience.

Locations

Country Name City State
Turkey Marmara University Pendik Training and Research Hospital Istanbul Pendik

Sponsors (1)

Lead Sponsor Collaborator
Janbubi Jandaulyet

Country where clinical trial is conducted

Turkey, 

References & Publications (1)

Celenlioglu AE, Sencan S, Gunduz OH. Does facet tropism negatively affect the response to transforaminal epidural steroid injections? A prospective clinical study. Skeletal Radiol. 2019 Jul;48(7):1051-1058. doi: 10.1007/s00256-018-3129-8. Epub 2019 Jan 2. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary NRS score =50% reduction in the NRS scores at month 3 relative to the initial NRS scores. at first hour, at three weeks, at 3 months
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