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

NCT05280301 · ClinicalTrials.gov registry record · NA

Multicenter Sous Vide Frostbite

A NA study of Frostbite and Frostbite of Hand, sponsored by Dartmouth-Hitchcock Medical Center.

Completed
Registry status
NA
Development phase
7
Enrollment target
1
Study location

NCT05280301: Completed NA study of Frostbite and Frostbite of Hand, sponsored by Dartmouth-Hitchcock Medical Center.

NCT05280301 is a NA study of Frostbite and Frostbite of Hand that has completed, run by Dartmouth-Hitchcock Medical Center. The registered enrollment target is 7 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05280301, a NA study of Frostbite and Frostbite of Hand, has completed, sponsored by Dartmouth-Hitchcock Medical Center.

COMPLETED
Registry status
NA
Development phase
7 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to determine the efficacy of using sous vide devices for heating and maintaining the circulating warm water bath used in the rewarming of acute frostbite.

Primary Outcome

Assess if frostbitten extremities can be thawed in a warm water bath created by the experimental device.

Interventions

  • DEVICE Sous Vide Device (SVD)

Study Locations (1)

New Hampshire

  • Dartmouth-Hitchcock Medical Center - Lebanon

Trial Details

FieldValue
Enrollment Target 7 participants
Start Date 2022-12-01
Est. Completion 2024-11-25
Phase NA
Dartmouth-Hitchcock Medical Center

427 total trials

What the finished NCT05280301 record still lists

NCT05280301 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 7 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 3 conditions, with Frostbite appearing as the primary indexed condition, and to 1 intervention - of which Sous Vide Device (SVD) is the first listed.

NCT05280301 reports a single indexed study location in New Hampshire.

Frequently Asked Questions

What is clinical trial NCT05280301 about?

NCT05280301 is a clinical study titled "Multicenter Sous Vide Frostbite". The purpose of this study is to determine the efficacy of using sous vide devices for heating and maintaining the circulating warm water bath used in the rewarming of acute frostbite.

What is the current status of trial NCT05280301?

This trial is currently completed. It is a NA study. The enrollment target is 7 participants. The study started on 2022-12-01. Estimated completion is 2024-11-25.

What conditions does trial NCT05280301 study?

This clinical trial studies the following conditions: Frostbite, Frostbite of Hand, Frostbite of Foot.

What interventions are being tested in trial NCT05280301?

The interventions under investigation include: Sous Vide Device (SVD) (DEVICE).

Who is sponsoring clinical trial NCT05280301?

This trial is sponsored by Dartmouth-Hitchcock Medical Center, which has 427 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05280301 being conducted?

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

Similar trials for Frostbite

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05280301's enrollment target sits among peer trials

7 1982nd of 2000 higher than 18 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 NCT05280301, the US trial registry maintained by the National Library of Medicine. NCT05280301 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.