Using Bioimpedance Analysis to Monitor Fluid Status in Children

Part of paid clinical trials in Memphis, Tennessee.

Sponsor
St. Jude Children's Research Hospital
Study ID
NCT07834710
Status
Not Yet Recruiting

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Conditions

  • Fluid Overload

Eligibility Criteria

Sex
ALL
Age
6 Years - 21 Years
Healthy Volunteers
Not accepted

Interventions

  • Bioimpedance device — DIAGNOSTIC_TEST
    Routine bioimpedance device measurements will be taken at specific times during the patient's initial hospitalization after the transplant. They will be performed alongside regular nursing assessments in the patient's hospital room.

Study Details

This study aims to develop a more comprehensive approach to monitoring fluid status in patients undergoing stem cell transplantation by combining conventional methods with a bioimpedance device.

Key Dates

First listed
Sep 22, 2026
Start date
Oct 31, 2026
Status verified
Sep 2026
Primary completion
Jun 30, 2027
Completion
Jun 30, 2027

Study Design

Enrollment
30 participants (estimated)

Arms

  • Arm: Hematopoietic stem cell transplantation (HSCT) recipients
    Participants ages 6-21 years planned to undergo allogeneic or autologous HSCT for any indication with any preparative regimen who meet the eligibility criteria and consent will be enrolled. Routine bioimpedance device measurements will be taken at specific times during the participant's initial hospitalization after the transplant.

Primary Outcome Measure

Feasibility of obtaining serial BIA-derived fluid markers during the initial HSCT hospitalization [ Time Frame: Baseline (before transplantation), Day 0 (on day of transplant), Day 1-14 (every other day for initial two weeks post-transplant), Once a week during the initial hospitalization post-transplantation up to one year ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
St. Jude Children's Research HospitalMemphisTennessee38105
[email protected]
888-226-4343

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By research site
St. Jude Children's Research Hospital· Memphis, TN

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