Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT05391178 · ClinicalTrials.gov registry record · NA

Improving Disease Severity

A NA study, sponsored by Wake Forest University Health Sciences.

Completed
Registry status
NA
Development phase
18
Enrollment target

NCT05391178: Completed NA study, sponsored by Wake Forest University Health Sciences.

NCT05391178 is a NA study that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 18 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05391178, a NA study, has completed, sponsored by Wake Forest University Health Sciences.

COMPLETED
Registry status
NA
Development phase
18 participants
Enrollment target

Study Summary

Phototherapy, including ultraviolet B (UVB) and ultraviolet A (UVA) light, has been used to treat a number of dermatologic conditions. Psoriasis is one of the most common conditions treated with phototherapy, in which phototherapy is often indicated for extensive disease with contraindications for other systemic treatments. The mechanism of action of phototherapy for the treatment of psoriasis is not completely understood; however, it is known that UVB light induces apoptosis of pathogenic T cells and keratinocytes, which may reduce the overactive immune response and epidermal hyperproliferation. Phototherapy has shown some efficacy for other diseases, such as alopecia areata (AA) and polymorphous light eruption (PMLE). However, phototherapy is not always an accessible treatment option for patients due to cost or lack of time.

Primary Outcome

Lesion photos

Interventions

  • OTHER Lumiton yarn sleeve
  • OTHER Lumiton yarn hat
  • OTHER Lumiton yarn shirt

Trial Details

FieldValue
Enrollment Target 18 participants
Start Date 2022-08-09
Est. Completion 2024-05-15
Phase NA
Wake Forest University Health Sciences

1,140 total trials

What the finished NCT05391178 record still lists

NCT05391178 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 18 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 3 interventions - of which Lumiton yarn sleeve is the first listed.

NCT05391178 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05391178 about?

NCT05391178 is a clinical study titled "Improving Disease Severity". Phototherapy, including ultraviolet B (UVB) and ultraviolet A (UVA) light, has been used to treat a number of dermatologic conditions. Psoriasis is one of the most common conditions treated with phototherapy, in which phototherapy is often indicated for extensive disease with contraindications for o...

What is the current status of trial NCT05391178?

This trial is currently completed. It is a NA study. The enrollment target is 18 participants. The study started on 2022-08-09. Estimated completion is 2024-05-15.

What interventions are being tested in trial NCT05391178?

The interventions under investigation include: Lumiton yarn sleeve (OTHER), Lumiton yarn hat (OTHER), Lumiton yarn shirt (OTHER).

Who is sponsoring clinical trial NCT05391178?

This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05391178's enrollment target sits among peer trials

18 1863rd of 2000 higher than 130 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01245179 · 18 participants · Phase 1

    Study of Panobinostat (LBH589) in Patients With Sickle Cell Disease

  • NCT01999361 · 18 participants · NA

    Prevention of de Novo Allosensitization in Islet Transplant Recipients Following Complete Graft Loss

  • NCT02359825 · 18 participants · Phase 1

    Nerve Repair Using Hydrophilic Polymers to Promote Immediate Fusion of Severed Axons and Swift Return of Function

  • NCT02870244 · 18 participants · Phase 1

    Adoptive T Cell Immunotherapy for Advanced Melanoma Using Engineered Lymphocytes

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT05391178, the US trial registry maintained by the National Library of Medicine. NCT05391178 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.