Intra-discal Injection of Platelet-rich Plasma (PRP) Enriched With Exosomes in Chronic Low Back Pain

Summary

Participation Requirements

Description

Eligibility and patient selection: This active control, randomized, double-blind trial will be conducted as per guidelines of Helsinki declaration on ethical conduct of human studies. Participants with a history of chronic LBP who met inclusion and exclusion criteria will be recruited. Participants ...

Eligibility and patient selection: This active control, randomized, double-blind trial will be conducted as per guidelines of Helsinki declaration on ethical conduct of human studies. Participants with a history of chronic LBP who met inclusion and exclusion criteria will be recruited. Participants will be evaluated by 2 interventional spine and medicine physicians. Eligible patients will be provided with the IRB-approved protocol and informed consent will be taken prior to study. PRP Preparation: Blood sample (60 ml) will be centrifuged at 600×g for 10 min to collect plasma fraction. And centrifuged at 4000×g for 15 min. Supernatant platelet poor plasma (PPP) will be then removed, leaving 1 ml PRP. PPP will be passed through one-micron special indigenous designed flush back filter (Alpha Corpuscle, Delhi, India) so that all the platelets present in PPP fraction will get trapped in the filter. These trapped platelets will be flushed back with 1 ml of PPP to retrieve most of the platelets. This will be mixed together and then passed through a WBC filter (Terumo Imuguard, USA) to filter off the leukocytes. The final PRP concentrate (0.1 ml) will be analysed for total leukocyte & platelet counts. Five samples will be selected randomly treated with bovine thrombin reconstituted in 10% calcium chloride will be assessed for growth factors [platelet-derived growth factors (PDGF) and vascular endothelial growth factors (VEGF)] by ELISA. On an average our PRP sample will have 100 billion platelets and 30x concentrate of blood platelet in 2ml of final PRP. Exosomes preparation: Sixty ml of blood in EDTA-coated tubes will be spin at 1,200 g for 10 minutes at 4°C to separate plasma. Plasma will be filtered with (0.22 ?m) filter. Avoid any pelleted material while transferring the plasma. Discard the pelleted material. This tube has special filter to concentrate exosomes and other growth promoting proteins. Tube will be centrifuged at 3000 g, RT, 30 min and exosomes will be collected and then will be concentrated (0.5 ml to 3ml). To recover exosomes clogged in wall of filter -add 20 ml NS (preferably PBS) into micro centrifuge tube and rinsed it by centrifugation at 3,500 g. Collect the concentrated soup of exosomes again which were clogged in filter wall. Quantification of protein content will be done by bicinchoninic acid (BCA) assay. Nanoparticle tracking analysis (NTA) Vesicle suspensions with concentrations between 1×107/ml and 1×109/ml will be examined using a Nanosight NS300 (NanoSight Ltd., UK) equipped with a 405 nm laser to determine the size and quantity of particles isolated. A video of 60-sec duration will be taken with a frame rate of 30 frames/sec, and particle movement will be analyzed using NTA software (version 2.3; NanoSight Ltd.). Western blot analysis The exosome supernatant will be denatured in sample buffer and will be subjected to western blot analysis. Purified exosomes will be analysed for protein expression HSP70, flottilin, CD63, TSG101 and calnexin. The proteins were visualized on the Bio-Rad ChemiDoc XRS Imager system (Bio-Rad Laboratories, Berkeley, CA, USA). Study Design Randomisation and Arms of the study: Approximately Three hundred patients will be screened to randomly allocate to treatment or control groups at a 1:1 ratio, to assign 30 patients into each 4 arm: Arm I will be assigned to receive placebo (trigger point injection under C arm) Arm II: to receive PRP with exosomes at the center of the nucleus pulposus (2ml) Test product(s), dose and mode of administration duration of treatment Patients will be randomly selected based on computer generated number to receive one undistinguishable injection of PRP ex or placebo. Following skin disinfection of the back 2 ml from the total PRPex procured was injected as soon as possible by an fluoroscopy guided lateral approach. Patients received the placebo in a similar manner but not to disc .it will be in muscles zone around trigger point .Physician who evaluated the study and patient were unknown of treatment. Patients were advised to continue with usual exercises, routine precautions, physiotherapy and back care. Paracetamol (to a maximum of up to one gram) three times a day, will be allowed to be used as a rescue drug. No systemic corticosteroid, potential symptom-modifying drug /procedure will be allowed during the study. Study assessments / Outcome measures Visual analog scale (VAS) Roland Morris Disability Questionnaire (RDQ) SF 36 health questionnaire Functional rating index MRI - disc degeneration grading, T2 quantification any evidence of discitis Patients will be assessed by visual analog scale (VAS), SF 36 health questionnaire, Functional rating index at baseline and followed at 1, 3, 6, and 12 months. The structural efficacy will evaluated by MRI t2 quantification and grading as described earlier in literature at baseline and at 6 months by two experienced radiologists. Assessors will be blinded. The patients will be evaluated for any adverse effects and vital signs once a week for the first month and then once a month up to 6 months. Blood samples were collected at the time of entry into the study, at six months, and on a final visit to examine biological variables as well as liver and kidney functions. Tolerability was assessed and laboratory-based haematological and biochemical assays were performed. A possible causal relationship with the treatment arm will also be assessed. Discontinuation from treatment with a specific reason will be ascertained. Any evidence of infection/discitis will be delicately observed. Worsening of pain will be deeply analyzed. STATISTICAL ANALYSIS: Analysis of variance (ANOVA) will be used to investigate the differences between groups. Differences in paired samples will be compared using the two-tailed Student's t-test. Correlations between variables will be assessed by Pearson's correlation. SPSS 20.0 will be used for statistical analyses (SPSS, Inc., Chicago, IL, USA). P<0.05 will be considered to be statistically significant. Identification of the relationship between safety issues/side effects and arousal level using measurement by rating scales. To test whether the relationship between safety issues/side effects and arousal level differs between IBRF ACP/MCP vs. Standard of Care groups, using measurement by rating scales, two analyses will be conducted. Canonical correlation will be used to determine which side effect (or combination of side effects) explains variance in the rating scale measurements. Additionally, cluster analysis will be employed to determine whether side effects are similarly related to arousal levels and outcomes for patients in the three treatment groups. MONITORING PROCEDURES/ADVERSE EVENTS / SAFETY ENDPOINTS Monitoring The monitors will visit the center during the study in addition to maintaining frequent telephone and written communication. The following guidelines meet the requirements specified in 21 CFR §812.46 and are provided to describe the procedures for monitoring the clinical studies. If the investigator is not complying with the signed Investigator Agreement, the protocol, or any condition of the study (e.g., incomplete data forms), the monitor has the right to terminate the investigator's participation in the study. Pre-Study Monitoring Procedures The designate (i.e. monitor) will be responsible for determining and documenting that each investigator clearly understands and accepts the responsibilities and obligations incurred in conducting a clinical study. The monitor will ensure prior to study initiation that the investigator: • Understands the requirements for a well-controlled study; • Understands the nature of the clinical protocol • Understands his/her reporting obligations; • Understands the requirements for device accountability; • Understands and accepts the obligations to obtain informed consent in accordance with 21 CFR Parts 50 and 56; • Understands and accepts the obligation to obtain IRB review and approval of the clinical investigation before it is initiated and to ensure continuing review of the study by the IRB in accordance with 21 CFR Part 56, and to keep the sponsor informed of all IRB actions concerning the study; • Understands and accepts the requirements regarding financial disclosure of clinical investigations, 21 CFR Part 54; • Has adequate facilities and access to an adequate number of suitable subjects to conduct the investigation; • Has the required documentation on file, including IRB approval and a signed investigator agreement. Periodic Monitoring Visits • Monitoring visits will be conducted in accordance with the FDA Guideline for the Monitoring of Clinical Investigations - January 1988. • The monitor should visit each site regularly to ensure the following: • Facilities continue to be adequate and acceptable. • The protocol is being properly followed. • The IRB/IEC has approved or been notified of any protocol changes. • Accurate, complete and current records are being maintained, and the information recorded. • Accurate, complete and timely adverse event reports are being submitted • Informed consent has been obtained. • The reason for a subject's withdrawal from the study has been documented. • Reports are being submitted to the IRB and sponsor. • The appropriate staff is carrying out study activities. • All case report forms and other documentation related to the study will be reviewed upon receipt, and the site will be promptly notified of any deficiencies. Frequency of Monitoring Visits a) Monitoring visits will be conducted according to standard monitoring procedures. Monitoring visits will be determined on the basis of several factors, including: b) Duration of the study; c) Number of outstanding issues from previous visits; d) Number of subjects enrolled; e) Number of investigators/sites; and, f) Complexity of the study. Study Termination All routine monitoring functions must be performed prior to the study termination visit. The study termination visit may be combined with a monitoring visit. The following tasks should be completed at the last visit by the monitor. a) Remind the investigator of the obligation to retain the records. b) Prepare final monitoring report for IEC. Reports of Monitoring Visits Monitoring reports must be completed for all visits. Reports must include the following information: a) Date of the visit; b) List of study site personnel present; c) A summary of the findings, problems

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