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NCT04967170 · ClinicalTrials.gov registry record · Phase 1

A Study to Evaluate Platelet Rich Plasma to Treat Vulvar Lichen Sclerosus

A Phase 1 study of Vulvar Lichen Sclerosus, sponsored by Jennifer R. Arthurs.

Active
Registry status
Phase 1
Development phase
30
Enrollment target
1
Study location

NCT04967170 is a Phase 1 study of Vulvar Lichen Sclerosus that is active but no longer recruiting, run by Jennifer R. Arthurs. The registered enrollment target is 30 participants. The trial reports 1 study location across 1 state.

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The verdict

NCT04967170, a Phase 1 study of Vulvar Lichen Sclerosus, is active but no longer recruiting, sponsored by Jennifer R. Arthurs.

ACTIVE NOT RECRUITING
Registry status
Phase 1
Development phase
30 participants
Enrollment target
1
Study location

Study Summary

The purposes of this study are to determine the safety and feasibility of autologous platelet-rich plasma for the treatment of vulvar lichen sclerosus, and to determine the efficacy of autologous platelet-rich plasma for the treatment of vulvar lichen sclerosus.

Conditions Studied

Interventions

  • OTHER Sham Procedure
  • BIOLOGICAL Autologous Platelet-Rich Plasma (PRP)

Study Locations (1)

Florida

  • Mayo Clinic in Florida - Jacksonville

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2022-01-19
Est. Completion 2026-06-02
Phase Phase 1

Sponsor

Jennifer R. Arthurs

1 total trials

What the Registry Record Tells You About NCT04967170

The ClinicalTrials.gov registry entry for NCT04967170 describes a study currently listed as active not recruiting, categorized as Phase 1. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Jennifer R. Arthurs, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Vulvar Lichen Sclerosus appearing as the primary indexed condition, and to 2 interventions - of which Sham Procedure is the first listed.

NCT04967170 reports 1 study location spanning 1 distinct geographic area - top geographies include Florida.

Frequently Asked Questions

What is clinical trial NCT04967170 about?

NCT04967170 is a clinical study titled "A Study to Evaluate Platelet Rich Plasma to Treat Vulvar Lichen Sclerosus". The purposes of this study are to determine the safety and feasibility of autologous platelet-rich plasma for the treatment of vulvar lichen sclerosus, and to determine the efficacy of autologous platelet-rich plasma for the treatment of vulvar lichen sclerosus.

What is the current status of trial NCT04967170?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 30 participants. The study started on 2022-01-19. Estimated completion is 2026-06-02.

What conditions does trial NCT04967170 study?

This clinical trial studies the following conditions: Vulvar Lichen Sclerosus.

What interventions are being tested in trial NCT04967170?

The interventions under investigation include: Sham Procedure (OTHER), Autologous Platelet-Rich Plasma (PRP) (BIOLOGICAL).

Who is sponsoring clinical trial NCT04967170?

This trial is sponsored by Jennifer R. Arthurs, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04967170 being conducted?

This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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