NCT07321028

Evaluation of In-Vitro Cryo Therapeutic Protocols on Human Cell Samples (TWH-CRYO-001)

Enrolling by Invitation
EARLY_PHASE1All AgesInterventionalTreatment
Truway Health, Inc.
~50 participants
Updated 2026-01-06 on ClinicalTrials.gov
What's tested:Standard Laboratory Cryopreservation ProcedureEnhanced Laboratory Cryopreservation ProcedureNormothermic Cell Culture Control

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Post-Thaw Viability
Measured over Twenty-four (24) hours after thaw
Cellular Injury and Post-Cryogenic Recovery
Cryogenic Cellular Stress
Cold-Induced Cellular Injury
Thermal Injury Response
Post-Thaw Viability Impairment
Osmotic Stress Injury
Biomechanical Injury Modeling (In-Vitro)
Blunt Force Injuries to the Extremities (Cellular Injury Model)
Tissue Damage and Recovery Pathways
Hypothermic Tissue Stress
Cellular Regeneration and Repair
1 sites across 1 states
New York1
  • Gavin Solomon, President & CEO · PRINCIPAL_INVESTIGATOR · Truway Health, Inc.

This trial hasn't published a contact. View it on ClinicalTrials.gov

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Eligibility criteria

Inclusion

This study does not enroll human participants. Eligibility applies only to human-derived cell samples.
Samples must be de-identified prior to receipt.
Samples must demonstrate ≥90% viability at pre-freeze assessment.
Samples must be free of contamination (bacterial, fungal, mycoplasma).
Samples must meet chain-of-custody and biospecimen compliance requirements.

Exclusion

No human participants will be enrolled or contacted.
Any specimen containing identifiable private information.
Samples with inadequate quality, contamination, or compromised viability.
Samples obtained without appropriate donor consent or de-identification certification.
  • Post-Thaw ViabilityTwenty-four (24) hours after thaw

    Percentage of viable cells determined by trypan blue exclusion assay or automated cell viability analyzer.