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RecruitingNCT06387212

35 kDa Hyaluronan Fragment (HA35) Reduces Chronic Inflammation of Skin

35 kDa Hyaluronan Fragment (HA35) Reduces Chronic Skin Inflammation

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
20 (estimated)
Sponsor
Nakhia Impex LLC · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

To explore the clinical effect and safety of 35 kDa hyaluronic acid fragment ( HA35 ) combined with negative pressure microneedle technology in improving skin problems.

Conditions

Interventions

TypeNameDescription
DRUG35 kDa hyaluronan fragment HA35 injectionFirst, apply an appropriate amount of compound lidocaine cream to the treatment site ( national drug approval number H20063466 ; Beijing Ziguang Pharmaceutical Co., Ltd. ) waited for 60 minutes after applying hemp, and then injected the syringe containing sterile HA35 prepared in advance into the subcutaneous 1.0-1.5mm through the DermaShine PRO negative pressure microneedle importer ( Demasha, South Korea ).

Timeline

Start date
2024-04-15
Primary completion
2024-05-01
Completion
2024-05-01
First posted
2024-04-26
Last updated
2024-05-21

Locations

1 site across 1 country: Mongolia

Source: ClinicalTrials.gov record NCT06387212. Inclusion in this directory is not an endorsement.