A Clinical Study of Freshly Manufactured 35kDa Hyaluronan Fragment in the Treatment of Pain
Primary Purpose
Shoulder Pain, Neck Pain, Back Pain
Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
HA35(L20200708MP07707, Ministry of Health, Mongolia) was freshly manufactured by mixing hyaluronidase PH20 injectable solution (H31022111) and high-molecular-weight HA injectable solution (H20174089)
Sponsored by
About this trial
This is an interventional treatment trial for Shoulder Pain focused on measuring hyaluronidase, Hyaluronan, 35kDa Hyaluronan fragment, pain caused by herpes zoster, pain caused by shoulder neck back and temporal
Eligibility Criteria
Inclusion Criteria: Shoulder, neck, back and temporal pain. The course of the disease ranged from 0 to 8 months. Herpes zoster pain. The course of 0-2 months. Exclusion Criteria: Individuals with severe spinal pathology (including fractures, inflammatory diseases and tumors)
Sites / Locations
- Qingdao University Affiliated Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
35kDa hyaluronan fragment HA35 injection
Arm Description
100 mg Hyaluronan is locally injected at the pain point or where the nerve trunk is innervated by the pain point.
Outcomes
Primary Outcome Measures
Pain scores of all shoulder, neck, back, temporal and herpes zoster pain
The pain scale is a tool that doctors use to help assess patients' pain. Each patient rated their pain on a scale of 0 to 10. 0 means "no pain" and 10 means "the most painful". Statistical t-test was used to calculate and evaluate the pain intensity, which was expressed as mean ±standard deviation.
Secondary Outcome Measures
Full Information
NCT ID
NCT05756595
First Posted
February 9, 2023
Last Updated
March 1, 2023
Sponsor
Dove Medical Press Ltd
Collaborators
The Affiliated Hospital of Qingdao University, Nakhia Impex LLC
1. Study Identification
Unique Protocol Identification Number
NCT05756595
Brief Title
A Clinical Study of Freshly Manufactured 35kDa Hyaluronan Fragment in the Treatment of Pain
Official Title
A Preliminary Clinical Study of Freshly Manufactured 35kDa Hyaluronan Fragment in the Treatment of Herpes Zoster Pain and Shoulder, Neck, Back and Temporal Pain
Study Type
Interventional
2. Study Status
Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
July 6, 2020 (Actual)
Primary Completion Date
December 29, 2022 (Actual)
Study Completion Date
February 8, 2023 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Dove Medical Press Ltd
Collaborators
The Affiliated Hospital of Qingdao University, Nakhia Impex LLC
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Local used high molecular weight Hyaluronan (HA) with high viscosity has a variety of receptors in the human body, including CD44, LYVE-1, RHAMM, HARE, Siglec-9, TLR2, CEMIP and TMEM2. Intra-articular local injection of HA has a certain degree of analgesic effect. Local injection of HA into the nerve trunk directed by ultrasound was used for the treatment of neuropathic pain. It was reported that the analgesic effect of HA is regulated by TRPV1 ion channels. This study hypothesizes that hyaluronidase cleaves HA to generate low molecular weight HA fragments HA35 with good tissue permeability, which may bind to a variety of HA receptors on the cell surface within the tissues and produce a broad-spectrum analgesic effect. In this study, 35kDa Hyaluronan fragment HA35 was prepared by mixing hyaluronidase PH20 injection and high molecular weight Hyaluronan (HA) injection at room temperature for 20 minutes. In this study, hyaluronidase injection and Hyaluronan injection were off-label used to conduct an investigator-initiated study (IIT or IIS) for the treatment of herpes zoster and shoulder, neck, back and temporal pain.
Detailed Description
Bioactive Hyaluronan fragment HA35 of 35kDa was isolated from human colostrum. Literature studies have shown that female breast hyaluronidase and male testicular sperm acrosomal hyaluronidase PH20 come from the same gene. The investigators, recombinant human hyaluronidase PH20 and neutral hyaluronidase (PH20 or SPAM1) of bovine testicular sperm acrosome were used to cleave macromolecular Hyaluronan. Regardless of the cutting time, the Hyaluronan fragment HA35 with an average molecular weight 35kDa was produced(Registration number L20200708MP07707, Ministry of Health, Mongolia). Hyaluronidase injection is often used to improve the penetration and absorption of other injectable drugs. Hyaluronidase injection is also used to degrade excessive use of cosmetic injection or improper use of cross-linked macromolecular Hyaluronan fillers, which is an off-label drug use of hyaluronidase(https://www.realself.com/news/ hyaluronidase-dissolve-fillers). In this study, Hyaluronan fragment HA35 of 35kDa was prepared by mixing hyaluronidase injection extracted from bovine testis (hyaluronidase for injection, H31022111) and Hyaluronan injection (sodium hyaluronate injection, H20174089) at room temperature for 20 minutes. Its analgesic effect on herpes zoster, shoulder, neck, back, and temporal pain was studied.
In this study, off-label drug use of hyaluronidase injection and Hyaluronan injection (https://www.realself.com/news/ hyaluronidase-dissolve-fillers)were used in the clinical study of shoulder, neck, back and temporal pain and herpes zoster pain, namely investigator initiated trails. In this clinical trial, 26 patients with shoulder, neck, back and temporal pain were studied in the Department of pain diagnosis and treatment of the affiliated Hospital of Qingdao University. Ten patients with herpes zoster were treated in the pain Department of the affiliated Hospital of Qingdao University. According to the ratio of 100mg high molecular Hyaluronan / 2000 unit hyaluronidase, the high molecular Hyaluronan injection (sodium hyaluronate injection, H20174089) and the hyaluronidase injection extracted from bovine testis (hyaluronidase for injection) were mixed at room temperature for 20 minutes. Each time according to the amount of high molecular Hyaluronan containing 100 mg Hyaluronan and hyaluronidase mixture, pain point area and pain point area of the nerve trunk innervation of the local multi-point injection. Then, pain scale was used to evaluate and record the pain relief of patients before and after treatment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Shoulder Pain, Neck Pain, Back Pain, Temporal Pain, Herpes Zoster Pain
Keywords
hyaluronidase, Hyaluronan, 35kDa Hyaluronan fragment, pain caused by herpes zoster, pain caused by shoulder neck back and temporal
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
A self-controlled an open label clinical study(An investigator-initiated off-label use clinical study)
Masking
None (Open Label)
Masking Description
A self-controlled an open label clinical study(An investigator-initiated off-label use clinical study)
Allocation
N/A
Enrollment
36 (Actual)
8. Arms, Groups, and Interventions
Arm Title
35kDa hyaluronan fragment HA35 injection
Arm Type
Experimental
Arm Description
100 mg Hyaluronan is locally injected at the pain point or where the nerve trunk is innervated by the pain point.
Intervention Type
Drug
Intervention Name(s)
HA35(L20200708MP07707, Ministry of Health, Mongolia) was freshly manufactured by mixing hyaluronidase PH20 injectable solution (H31022111) and high-molecular-weight HA injectable solution (H20174089)
Other Intervention Name(s)
HA35
Intervention Description
This group will inject once a week. Evaluation of pain score after 30 seconds and 3 hours.
Primary Outcome Measure Information:
Title
Pain scores of all shoulder, neck, back, temporal and herpes zoster pain
Description
The pain scale is a tool that doctors use to help assess patients' pain. Each patient rated their pain on a scale of 0 to 10. 0 means "no pain" and 10 means "the most painful". Statistical t-test was used to calculate and evaluate the pain intensity, which was expressed as mean ±standard deviation.
Time Frame
3 hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
39 Years
Maximum Age & Unit of Time
63 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Shoulder, neck, back and temporal pain. The course of the disease ranged from 0 to 8 months.
Herpes zoster pain. The course of 0-2 months.
Exclusion Criteria:
Individuals with severe spinal pathology (including fractures, inflammatory diseases and tumors)
Facility Information:
Facility Name
Qingdao University Affiliated Hospital
City
Qingdao
State/Province
Shandong
ZIP/Postal Code
266000
Country
China
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Time Frame
published precinical study and international granted patent
IPD Sharing Access Criteria
Anti-Inflammatory Effects of the 35kDa Hyaluronic Acid Fragment (B-HA/HA35); APPLICATION OF LOW-MOLECULAR-WEIGHT HYALURONIC ACID(LMW-HA) FRAGMENTS(INJECTION) WO/2017/186088 US20200254005 EP3479830 AU2017255833 CA3049286
IPD Sharing URL
http://www.dovepress.com/articles.php?article_id=80993;https://patentscope.wipo.int/search/en/detail.jsf?docId=CA249072967&_cid=P22-LDWT33-38680-1
Citations:
PubMed Identifier
36686276
Citation
Jia X, Shi M, Wang Q, Hui J, Shofaro JH, Erkhembayar R, Hui M, Gao C, Gantumur MA. Anti-Inflammatory Effects of the 35kDa Hyaluronic Acid Fragment (B-HA/HA35). J Inflamm Res. 2023 Jan 13;16:209-224. doi: 10.2147/JIR.S393495. eCollection 2023.
Results Reference
result
Citation
APPLICATION OF LOW-MOLECULAR-WEIGHT HYALURONIC ACID(LMW-HA) FRAGMENTS(INJECTION) WO/2017/186088 US20200254005 EP3479830 AU2017255833 CA3049286
Results Reference
result
Links:
URL
http://patentscope.wipo.int/search/en/detail.jsf?docId=CA249072967&_cid=P22-LDWT33-38680-1
Description
Related Info
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A Clinical Study of Freshly Manufactured 35kDa Hyaluronan Fragment in the Treatment of Pain
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