Failed Back Surgery Syndrome Clinical Trial
— LASPINEOfficial title:
Analysis of Effect of Low Level Laser Therapy in Spinal Surgery
Verified date | June 2018 |
Source | University of Nove de Julho |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Each year, more than one million individuals worldwide are submitted to laminectomies, with a failure rate higher than 40%. Postlaminectomy epidural adhesion is implicated as a main cause of ''failed back surgery syndrome'' and associated with increased risk of complications during revision surgery. The postoperative epidural scar can cause extradural compression or dural tethering, which results in recurrent radicular pain and physical impairment. Several studies in the literature are signalizing that Low-Level-Laser-Therapy (LLLT) is proven to be an effective tool to assist the inflammatory process and wound healing, as well to prevent infection. Thus, the objectives of this project are to delineate and evaluate the LLLT effects in spinal surgery. A prospective randomized, controlled trial with a total of 48 patients who underwent laminectomy, were divided into 2 groups. In the first group, 25 patients received LLLT during the surgical procedure over dura mater, over subcutaneous and on the skin, as well as 24h and 72h post surgery. In the second group, 23 patients were induced to think they will be getting the same treatment, although the laser is not operating. In those groups, C reactive protein, Lactate Dehydrogenase and Creatine kinase were evaluated in the second and fifth days after surgery, digital temperature will be measured and scores in visual analogue scale will be used, 5 minutes pre and 5 minutes post Laser application. The drainage output was collected in the first three days following surgery in both groups. Interleukins were evaluated in interstitial infiltrate drained in 24h and 48h. The data was evaluated for normality and subjected to appropriate statistical analysis, in order to seek representation, as same as the level of significance of the studied samples.
Status | Completed |
Enrollment | 48 |
Est. completion date | June 2018 |
Est. primary completion date | November 2015 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 10 Years to 90 Years |
Eligibility |
Inclusion Criteria: - Patients undergoing to lumbar laminectomy Exclusion Criteria: - Active lumbar cancer - Infectious disease - Coagulation disorders - Dural injury during the surgery |
Country | Name | City | State |
---|---|---|---|
Brazil | Nove de Julho Universtiy | Sao Paulo | São Paulo |
Lead Sponsor | Collaborator |
---|---|
University of Nove de Julho |
Brazil,
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* Note: There are 14 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Temperature of the skin in the healing scar | Verified 1 minute before and 1 minute after LLLT | pre and 1 minute post LLLT | |
Other | Values of Creatine Kinase in the blood | Obtained through patient blood. | pre operative, 24h and 48h postoperative | |
Other | Values of C reactive protein in the blood | Obtained through patient blood pre operative, 24h and 48h postoperative | pre operative, 24h and 48h postoperative | |
Other | Values of Lactate dehydrogenase in the blood | Obtained through patient blood pre operative, 24h and 48h postoperative | pre operative, 24h and 48h postoperative | |
Primary | Immunochemistry to evaluate low level laser therapy anti-inflammatory mechanism 24 hours | Interstitial infiltrate obtained of Lumbar Drain collected 24 hours after surgery, interleukins IL-1, IL-4, IL-8, IL-10 and TNF alfa were measured through Immunochemistry, using ELISA. | 24 hours after surgery | |
Primary | Immunochemistry to evaluate low level laser therapy mechanism 48 hours after light delivery | Interstitial infiltrate was obtained of Lumbar Drain collected 48 hours after surgery, in this infiltrate interleukins IL-1, IL-4, IL-8, IL10 and TNF alfa were measured through Immunochemistry, using ELISA. | 48h after surgery | |
Secondary | Score in Visual Analogue Scale | Patient had to choose between 0 and 10 on the 11 point short pain scale. | 5 minutes pre LLLT | |
Secondary | Score in Visual Analogue Scale | Change from baseline in pain on the 11 point short pain scale. | 5 minutes post LLLT |
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