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NCT03313999 · ClinicalTrials.gov registry record · NA

Measuring Skin Elasticity in Lymphedema Patients

A NA study, sponsored by Beth Israel Deaconess Medical Center.

Terminated
Registry status
NA
Development phase
7
Enrollment target

NCT03313999: Clinical Trial NA study, sponsored by Beth Israel Deaconess Medical Center.

NCT03313999 is a NA study that was terminated before completion, run by Beth Israel Deaconess 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). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03313999, a NA study, was terminated before completion, sponsored by Beth Israel Deaconess Medical Center.

TERMINATED
Registry status
NA
Development phase
7 participants
Enrollment target

Study Summary

This protocol will utilize the lymphedema indentometer, or durometer (a novel, noninvasive piece of equipment that measures skin elasticity), to better characterize disease progression in patients with lymphedema. Beth Israel Deaconess Medical Center patients who undergo treatment of lymphedema will be candidates for this noninvasive test. This device and the data it generates will help understand the incidence of lymphedema at Beth Israel Deaconess Medical Center compared to national data and the outcomes of surgical treatment of lymphedema.

Primary Outcome

Value providing measure for the viscoelastic properties of skin including firmness and mechanical creep.

Interventions

  • DEVICE Lymphedema Indentometer

Trial Details

FieldValue
Enrollment Target 7 participants
Start Date 2018-02-18
Est. Completion 2025-06-02
Phase NA

Why NCT03313999 stopped before completion

NCT03313999 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 0 conditions, and to 1 intervention - of which Lymphedema Indentometer is the first listed.

NCT03313999 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03313999 about?

NCT03313999 is a clinical study titled "Measuring Skin Elasticity in Lymphedema Patients". This protocol will utilize the lymphedema indentometer, or durometer (a novel, noninvasive piece of equipment that measures skin elasticity), to better characterize disease progression in patients with lymphedema. Beth Israel Deaconess Medical Center patients who undergo treatment of lymphedema will...

What is the current status of trial NCT03313999?

This trial is currently terminated. It is a NA study. The enrollment target is 7 participants. The study started on 2018-02-18. Estimated completion is 2025-06-02.

What interventions are being tested in trial NCT03313999?

The interventions under investigation include: Lymphedema Indentometer (DEVICE).

Who is sponsoring clinical trial NCT03313999?

This trial is sponsored by Beth Israel Deaconess Medical Center, which has 488 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03313999'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

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Source: ClinicalTrials.gov NCT03313999, the US trial registry maintained by the National Library of Medicine. NCT03313999 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.