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Clinical Trials/NCT05403775
NCT05403775UnknownNot Applicable

Application of 3D Printing Guide Plate in Transforaminal Epidural Steroid Injection (TFESI) Combined With Pulsed Radiofrequency (PRF) Treatment

Peking University Third Hospital1 site in 1 country40 target enrollmentStarted: July 8, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
40
Locations
1
Primary Endpoint
C-arm fluoroscopy times

Study Overview

Brief Summary

This study applies 3D-printed customized guide plate in assisting the accurate puncture in transforaminal epidural steroid injection (TFESI) combined with pulsed radiofrequency (PRF) treatment. This technique can shorten reduce the intra-operative radiation, and do not affect the surgical outcome.

Detailed Description

Lumbar disc herniation (LDH) is a common degenerative spine disease and it can cause low back pain and lumbosacral radicular pain (LSRP). Transforaminal epidural steroid injection (TFESI) is one of the most common minimally invasive interventions for the treatment of LDH. TFESI combined with dorsal root ganglion pulsed radiofrequency (PRF) is an effective procedure for treating LSRP. Needle Puncture is the key technology in this procedure.

In the past when there were no customized guides, the surgeons would place the needle according to his/her previous experience under the guidance of C-arm fluoroscopy or CT. If the position of the needles is not satisfactory, repeated procedure will be performed. This would lead to an increase in the duration of surgery and intra-operative radiation, which is detrimental to both the surgeon and the patient. This problem is well solved by applying the 3D printing guide plate.

The application procedure for the the 3D printing guide plate: the model of the spine is established according to the patient's CT scan data to prepare the customized guide plate, then sterilize them for future use. The final position of needle is confirmed by C-arm fluoroscopy or CT.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Age ≥18 years old,
  • •Chronic lumbosacral radicular pain lasting ≥12 weeks,
  • •Dominant leg pain with less intense back pain,
  • •The previous failure of conservative management such as physiotherapy, exercise therapy, or analgesic medications,
  • •Pain intensity≥4 out of 10 on the numerical rating scale (NRS),
  • •Segmental pain of a radicular nature originating from the lumbar segments and with a shooting or lancinating quality corresponding to a dermatome suggestive of the involved nerve root,
  • •Availability of computed tomography/magnetic resonance imaging findings of pathology concordant with the side and level of their clinical features.

Exclusion Criteria

  • •Patient refusal to participate in the study,
  • •Pregnant or nursing
  • •Progressive motor weakness in the affected leg,
  • •Allergies to local anesthetics, contrast dyes or steroids
  • •Significant anatomic deformity (either congenital or acquired) making it difficult to access the foramen as evidenced by computed tomography/magnetic resonance imaging
  • •Presence of cancer accounting for back pain
  • •Patients with platelet dysfunction, bleeding disorder or continuing anticoagulant treatment
  • •Steroid injection within the previous 12 weeks,
  • •Systemic infection,
  • •Injection site infection,
  • •Unstable medical or psychiatric condition

Arms & Interventions

3D printing guide plate group

Experimental

3D-printed customized guide plate will be used to guide the puncture in TFESI combined with dorsal root ganglion PRF.

Intervention: 3D printing guide plate (Other)

Conventional guidance group

Active Comparator

The surgeons would place the needle according to his/her previous experience under the guidance of C-arm fluoroscopy.

Intervention: Conventional guidance (Other)

Outcomes

Primary Outcomes

C-arm fluoroscopy times

Time Frame: Intraoperative

Numbers of using C-arm fluoroscopy

Secondary Outcomes

  • Numerical rating scale (NRS)(Postoperative 1 day, 1 month, 3 months)
  • MacNab(Postoperative 3 months)
  • Complications(Intraoperative)
  • Puncture time(Intraoperative)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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