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HA35 Treatment the Gingival Discomfort as Well as Gingival Redness and Bleeding of Patients With Periodontitis

Primary Purpose

Periodontitis

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
Dove Medical Press Ltd
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Periodontitis focused on measuring 35 kDa low molecular hyaluronan fragment, HA35, Tissue permeability, Intra-pocket injection, Gingival redness and bleeding

Eligibility Criteria

32 Years - 62 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Mild periodontitis and associated with gingival discomfort or itchiness. Patient > 18 years old. Systemically healthy individuals Exclusion Criteria: Patients who take Anticoagulants or Antiplatelet Agents Pregnant or breastfeeding women Patient having expressed his opposition to participate in the research.

Sites / Locations

  • Huinuode Biotechnology Co., Ltd.

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

35kDa hyaluronan fragment HA35 injection

Arm Description

The investigator injected 35kDa hyaluronan fragment HA35 into the periodontal pocket in a single dose of 100 mg.The distribution of injection amount was determined by the location of gingival inflammation.

Outcomes

Primary Outcome Measures

Gingival discomfort scores
This study used a modified pain scale to assess gingival discomfort or itching relief. This quantitative assessment represents the degrees of relief of gingival discomfort. Each patient rated their gingival discomfort or itching on a scale of 0 to 10. 0 means "no gingival discomfort or itching" and 10 means "worst gingival discomfort or itching". Pain intensity levels were assessed before and after 7 days of treatment.

Secondary Outcome Measures

The scores of reduction in the extent of gingival redness and swelling and the reduction in gingival bleeding.
Measurement of gum redness and swelling The physician used the numbers 0-10 to rate the intensity of gingival redness and swelling in the subject. 0 means "no gingival redness and swelling"; 10 means "highest intensity of gingival redness and swelling", which is the state of gingival redness and swelling before treatment.
The scores of reduction in gingival bleeding.
Measurement of probe gingival bleeding The physician used the numbers 0-10 to rate the extent to which the subject's probe gums were bleeding. 0 indicating "no gingival bleeding" and 10 indicating "most gingival bleeding from the probe", which is the pre-treatment state.

Full Information

First Posted
February 22, 2023
Last Updated
August 13, 2023
Sponsor
Dove Medical Press Ltd
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1. Study Identification

Unique Protocol Identification Number
NCT05765513
Brief Title
HA35 Treatment the Gingival Discomfort as Well as Gingival Redness and Bleeding of Patients With Periodontitis
Official Title
Intra-pocket Injection of a Freshly Manufactured 35 kDa Hyaluronan Fragment HA35 Reduces the Gingival Discomfort as Well as Gingival Redness and Bleeding of Patients With Periodontitis: A Clinical Study
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
February 2, 2023 (Actual)
Primary Completion Date
July 20, 2023 (Actual)
Study Completion Date
August 11, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Dove Medical Press Ltd

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
The main objective of this study is to research the treatment of 35 kDa hyaluronan fragment HA35 for Mild periodontitis and associated with gingival discomfort or itchiness.
Detailed Description
In this study, tissue permeable 35 kDa low molecular hyaluronan fragment HA35 was freshly manufactured using pharmaceutical grade hyaluronidase PH20 injection (State Drug Administration H31022111) and joint cavity HA injection (State Drug Administration H20174089) mixed at room temperature for 20 min. In this study, 20 patients, 8 males, and 12 females, with a mean age of 47±15 years, were selected from the outpatient clinic of the Department of Dentistry, Sanya Central Hospital. All had mild periodontitis and were associated with gingival discomfort or itchiness. Injection treatment was performed using freshly manufactured 35 kDa hyaluronan fragment HA35. The study was an open-label clinical trial in which no information was withheld from the participating investigators. A pre- and post-treatment controlled study approach was used, whereby the investigator injected 35kDa hyaluronan fragment HA35 into the periodontal pocket in a single dose of 100 mg. The distribution of injection amount was determined by the location of gingival inflammation. The clinical effects of gingival discomfort or itching, redness and swelling, and bleeding from the probing were observed and recorded in patients before and after 7 days of treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Periodontitis
Keywords
35 kDa low molecular hyaluronan fragment, HA35, Tissue permeability, Intra-pocket injection, Gingival redness and bleeding

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
an open-label, single-arm clinical study comparing pre- and post-treatment effects
Masking
None (Open Label)
Masking Description
an open-label, single-arm clinical study comparing pre- and post-treatment effects
Allocation
N/A
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
35kDa hyaluronan fragment HA35 injection
Arm Type
Experimental
Arm Description
The investigator injected 35kDa hyaluronan fragment HA35 into the periodontal pocket in a single dose of 100 mg.The distribution of injection amount was determined by the location of gingival inflammation.
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
The clinical effects of gingival discomfort oritching, redness and swelling, and bleeding from the probing were observed and recorded in patients before and after 7 days of treatment.
Primary Outcome Measure Information:
Title
Gingival discomfort scores
Description
This study used a modified pain scale to assess gingival discomfort or itching relief. This quantitative assessment represents the degrees of relief of gingival discomfort. Each patient rated their gingival discomfort or itching on a scale of 0 to 10. 0 means "no gingival discomfort or itching" and 10 means "worst gingival discomfort or itching". Pain intensity levels were assessed before and after 7 days of treatment.
Time Frame
7 days
Secondary Outcome Measure Information:
Title
The scores of reduction in the extent of gingival redness and swelling and the reduction in gingival bleeding.
Description
Measurement of gum redness and swelling The physician used the numbers 0-10 to rate the intensity of gingival redness and swelling in the subject. 0 means "no gingival redness and swelling"; 10 means "highest intensity of gingival redness and swelling", which is the state of gingival redness and swelling before treatment.
Time Frame
7 days
Title
The scores of reduction in gingival bleeding.
Description
Measurement of probe gingival bleeding The physician used the numbers 0-10 to rate the extent to which the subject's probe gums were bleeding. 0 indicating "no gingival bleeding" and 10 indicating "most gingival bleeding from the probe", which is the pre-treatment state.
Time Frame
7 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
32 Years
Maximum Age & Unit of Time
62 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Mild periodontitis and associated with gingival discomfort or itchiness. Patient > 18 years old. Systemically healthy individuals Exclusion Criteria: Patients who take Anticoagulants or Antiplatelet Agents Pregnant or breastfeeding women Patient having expressed his opposition to participate in the research.
Facility Information:
Facility Name
Huinuode Biotechnology Co., Ltd.
City
Qingdao
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
Citation
APPLICATION OF LOW-MOLECULAR-WEIGHT HYALURONIC ACID(LMW-HA) FRAGMENTS(INJECTION) WO/2017/186088 US20200254005 EP3479830 AU2017255833 CA3049286
Results Reference
background
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
Links:
URL
http://patentscope.wipo.int/search/en/detail.jsf?docId=CA249072967&_cid=P22-LDWT33-38680-1DescriptionRelatedInfo
Description
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HA35 Treatment the Gingival Discomfort as Well as Gingival Redness and Bleeding of Patients With Periodontitis

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