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Clinical Trial

Hyaluronidase Via LADD Scleroderma-induced Microstomia

NCT: NCT05995626 · COMPLETED

NCT IDNCT05995626
StatusCOMPLETED
Start Date2024-03-01
Completion2024-09-24

Brief Summary

Two treatment methods, ablative carbon dioxide (CO2) laser and intradermal hyaluronidase, will be combined to maximize the beneficial potential of each. Laser-assisted drug delivery (LADD) has been shown to be effective for the administration of medications in diverse skin diseases but not previously reported for the treatment of scleroderma-induced microstomia. By using this laser technique, the investigator can reduce the pain of typical hyaluronidase injections and reap the therapeutic benefit of the laser treatment itself. The investigator's goal is to create greater mouth mobility for chewing and speaking as well as improved oral hygiene, self-esteem, and overall quality of life. Each participant will undergo three separate laser sessions at 4 to 8-week intervals. Participants will also complete a follow-up visit three months after the last laser session to evaluate the response.

Frequently Asked Questions

What is Hyaluronidase Via LADD Scleroderma-induced Microstomia?

Hyaluronidase Via LADD Scleroderma-induced Microstomia is a clinical trial registered under NCT05995626. Current status: COMPLETED.

What is the status of NCT05995626?

The current status of NCT05995626 (Hyaluronidase Via LADD Scleroderma-induced Microstomia) is: COMPLETED.

When did Hyaluronidase Via LADD Scleroderma-induced Microstomia start?

Hyaluronidase Via LADD Scleroderma-induced Microstomia started on 2024-03-01.

Official Source

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Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.