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

NCT05944250 · ClinicalTrials.gov registry record · NA

A Pilot Study to Evaluate a Temporary Skin Substitute (Spincare® Matrix) for Wound Healing in RDEB Patients

A NA study, sponsored by Stanford University.

Completed
Registry status
NA
Development phase
6
Enrollment target

NCT05944250: Completed NA study, sponsored by Stanford University.

NCT05944250 is a NA study that has completed, run by Stanford University. The registered enrollment target is 6 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist → Add completion date to calendar (.ics) →

The verdict

NCT05944250, a NA study, has completed, sponsored by Stanford University.

COMPLETED
Registry status
NA
Development phase
6 participants
Enrollment target

Study Summary

Recessive dystrophic epidermolysis bullosa (RDEB) is a subtype of epidermolysis bullosa (EB), an inherited skin condition that presents with blistering skin. The Spincare device, developed by Nanomedic, is the first portable tool that delivers a non-invasive, non-therapeutic electrospun, nanofibrous matrix dressing to wounds to promote healing. The aim of this study is to determine the suitability of this device in RDEB wounds and assess its wound healing properties, safety and tolerability.

Primary Outcome

The primary endpoint was comparison of the duration of wound closure of matrix-treated wounds vs control wounds measured as the number of wounds achieving greater than 90% wound closure within 4 months

Interventions

  • DEVICE Spincare matrix

Trial Details

FieldValue
Enrollment Target 6 participants
Start Date 2023-09-19
Est. Completion 2024-08-14
Phase NA
Stanford University

1,744 total trials

What the finished NCT05944250 record still lists

NCT05944250 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 6 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower).

The record links to 0 conditions, and to 1 intervention - of which Spincare matrix is the first listed.

NCT05944250 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05944250 about?

NCT05944250 is a clinical study titled "A Pilot Study to Evaluate a Temporary Skin Substitute (Spincare® Matrix) for Wound Healing in RDEB Patients". Recessive dystrophic epidermolysis bullosa (RDEB) is a subtype of epidermolysis bullosa (EB), an inherited skin condition that presents with blistering skin. The Spincare device, developed by Nanomedic, is the first portable tool that delivers a non-invasive, non-therapeutic electrospun, nanofibrous...

What is the current status of trial NCT05944250?

This trial is currently completed. It is a NA study. The enrollment target is 6 participants. The study started on 2023-09-19. Estimated completion is 2024-08-14.

What interventions are being tested in trial NCT05944250?

The interventions under investigation include: Spincare matrix (DEVICE).

Who is sponsoring clinical trial NCT05944250?

This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05944250's enrollment target sits among peer trials

6 1983rd of 2000 higher than 13 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 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 NCT05944250, the US trial registry maintained by the National Library of Medicine. NCT05944250 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.