Clinical Study of Treatment of Acute Spinal Cord Injury by Near Infrared Light Irradiation

Spinal Cord Injuries Clinical Trial

Official title:

Clinical Study of Treatment of Acute Spinal Cord Injury by Near Infrared Light Irradiation

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03643419
• Other study ID #: KY20172036-1
• Status: Recruiting
• Phase: N/A
• Start date: September 1, 2018
• Est. completion date: December 30, 2019

Study information

• Verified date: August 2018
• Source: Xijing Hospital
• Contact: Tan Ding
• Phone: +86 13992825000
• Email: xijing_lllt[@]163.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study was to observe the therapeutic effect of near-infrared light irradiation on the treatment of acute spinal cord injury in humans, and whether it can promote the recovery of neurological function. Half of the patients underwent laminectomy and decompression surgery, and the other half of the patients were implanted with irradiated fibers for irradiation after surgery.

Description:

The annual incidence of spinal cord injury has increased year by year, and there is currently no effective treatment.

Near-infrared light has been widely used in clinical medicine because of its bio-stimulating effect, convenient use, harmless to the body, easy to be accepted by patients, and convenient for clinical promotion. The near-infrared light biostimulation effect can enhance the activity of various enzymes, inhibit inflammatory cells, inhibit neuronal apoptosis, and promote nerve regeneration. It has been widely confirmed and widely used in the rehabilitation of central nervous system and peripheral nerve injury. However, the position of the spinal cord is deep, and the depth of illumination used by laser treatment equipment is generally difficult to reach.

The implantable 360° scattering fiber the investigators developed was implanted in the surgical site together with the drainage tube for irradiation treatment without additional patient damage.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: December 30, 2019
• Est. primary completion date: June 30, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 20 Years to 70 Years

Eligibility

Inclusion Criteria:

• Diagnosed as acute spinal cord injury (ASIA grade A-C) (thoracic segment) requiring surgical laminectomy

• The patient determined by the investigator to be eligible for the illuminating fiber implanted in this clinical trial

• The patient fully understands the content and requirements of this clinical trial and is able to complete the follow-up according to the time specified in the protocol

• Voluntary participation in clinical validation and signing informed consent

Exclusion Criteria:

• The patient has a systemic infection or a local infection at the target surgical site

• The patient has more than 2 segments of spinal cord injury, and the vital signs are unstable

• A patient with a malignant tumor that does not involve the target surgical site

• Patient life expectancy is less than one year

• Pregnant or lactating women

• The patient is too obese, BMI = 40

• Patients with other systemic diseases who are using corticosteroids, or patients with growth factors, or long-term use of non-steroidal anti-inflammatory drugs

• Patients have a history of endocrine diseases affecting bone metabolism (such as diabetes, metabolic bone disease, etc.) or autoimmune diseases (such as multiple sclerosis)

• Alcohol abuse within one year (average daily alcohol consumption > 40g, equivalent to 50ml alcohol 50ml, or smoking = 40 / day, or drug abusers)

• Participating in other drug or device clinical trials

Related Conditions & MeSH terms

• Near Infrared Light Irradiation
• Neurological Rehabilitation
• Photobiology
• Spinal Cord Injuries
• Wounds and Injuries

Intervention

Procedure:
• Laminectomy
According to the standard procedure of laminectomy for acute spinal cord injury

Device:
• Spinal nerve laser therapeutic apparatus(Composed of 808-band fully automatic control laser device and implantable 360° scattering medical fiber)
According to the standard procedure of decompression of laminectomy for acute spinal cord injury, the patient in the Near Infrared Light Irradiation Group placed the implantable 360° scattering fiber laterally above the operation area at the end of the operation. Near infrared light irradiation is applied by spinal nerve laser therapeutic apparatus every day from the day after surgery, once a day for 60 minutes each time.

Locations

Country	Name	City	State
China	Xijing Hospital	Xi'an	Shaanxi

Sponsors (1)

Lead Sponsor	Collaborator
Xijing Hospital

Country where clinical trial is conducted

China, 

References & Publications (4)

Black B, Vishwakarma V, Dhakal K, Bhattarai S, Pradhan P, Jain A, Kim YT, Mohanty S. Spatial temperature gradients guide axonal outgrowth. Sci Rep. 2016 Jul 27;6:29876. doi: 10.1038/srep29876. — View Citation

Chen YJ, Wang YH, Wang CZ, Ho ML, Kuo PL, Huang MH, Chen CH. Effect of low level laser therapy on chronic compression of the dorsal root ganglion. PLoS One. 2014 Mar 4;9(3):e89894. doi: 10.1371/journal.pone.0089894. eCollection 2014. — View Citation

Khan I, Tang E, Arany P. Molecular pathway of near-infrared laser phototoxicity involves ATF-4 orchestrated ER stress. Sci Rep. 2015 Jun 1;5:10581. doi: 10.1038/srep10581. — View Citation

Sekhon LH, Fehlings MG. Epidemiology, demographics, and pathophysiology of acute spinal cord injury. Spine (Phila Pa 1976). 2001 Dec 15;26(24 Suppl):S2-12. Review. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change from Baseline ASIA Rating Scale at 6 Months	The ASIA rating scale was used to evaluate the patient's function, and the scores of each major item were obtained according to the weighting factors of each major item, with a total score of 0 to 100 points.	6 Months
Primary	Change from Baseline ASIA Rating Scale at 12 Months	The ASIA rating scale was used to evaluate the patient's function, and the scores of each major item were obtained according to the weighting factors of each major item, with a total score of 0 to 100 points.	12 Months
Primary	Change from Baseline EMG at 6 Months	The motor evoked potentials(MEP) and sensory evoked potentials(SEP) were evaluated, and the differences in the latency of the evoked potential N1 wave between the two groups were compared.	6 Months
Primary	Change from Baseline EMG at 12 Months	The motor evoked potentials(MEP) and sensory evoked potentials(SEP) were evaluated, and the differences in the latency of the evoked potential N1 wave between the two groups were compared.	12 Months