Application of 3D Printing Guide Plate in Percutaneous Disc Decompression

Peking University

Status: Not yet enrolling

Conditions: 3D Printing Guide Plate; Percutaneous Disc Decompression; Radicular Pain; Radiculopathy; Lumbar Disc Herniation; Discogenic Pain; Low Back Pain

Treatments: Other: Conventional guidance; Other: 3D printing guide plate

Study type: Interventional

Funder types: Other

Identifiers

NCT05610553

TTK03

Details and patient eligibility

About

Application of 3D printing guide plate in percutaneous disc decompression

Full description

This study applies 3D-printed customized guide plate in assisting the accurate puncture in percutaneous disc decompression, in patients with low back pain, lumbosacral radicular pain, disogenic pain, lumbar disc herniation, disc degeneration, etc. This technique can shorten reduce the intra-operative radiation, and do not affect the surgical outcome.

This study involved diseases such as lumbar disc herniation (LDH), disc degeneration, etc. Percutaneous disc decompression surgeries are effective treatments for these disease. Needle Puncture is the key technology in percutaneous disc decompression surgeries.

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 could be well solved by applying the 3D printing guide plate.

The key processes for the 3D printing guide plate procedure: the model of the spine or bone 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 or evoked pain.

Enrollment: 32 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Age ≥18 years old;
2. Pain lasting ≥12 weeks;
3. The previous failure of conservative management such as physiotherapy, exercise therapy, or analgesic medications;
4. Pain intensity≥4 out of 10 on the numerical rating scale (NRS);
5. Availability of computed tomography/magnetic resonance imaging findings of pathology concordant with the side and level of their clinical features;
6. Agree with percutaneous disc decompression.

Exclusion criteria

1. Patient refusal to participate in the study;
2. Pregnant or nursing;
3. Allergies to local anesthetics, contrast dyes or steroids;
4. Significant anatomic deformity (either congenital or acquired) making it difficult to access the target as evidenced by computed tomography/magnetic resonance imaging;
5. Patients with platelet dysfunction, bleeding disorder or continuing anticoagulant treatment;
6. Systemic infection;
7. Injection site infection;
8. Unstable medical or psychiatric condition;
9. Unable to tolerate the surgeries.

Trial design

Primary purpose: Other

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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32 participants in 2 patient groups

3D printing guide plate group

Experimental group

Description:

3D-printed customized guide plate will be used to guide the puncture in percutaneous disc decompression surgeries.

Treatment:

Other: 3D printing guide plate

Conventional guidance group

Active Comparator group

Description:

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

Treatment:

Other: Conventional guidance