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

NCT02710162 · ClinicalTrials.gov registry record · Early Phase 1

Accurate Screening Tools for Dysphagia in Amyotrophic Lateral Sclerosis (ALS)

A Early Phase 1 study, sponsored by University of Florida.

Completed
Registry status
Early Phase 1
Development phase
21
Enrollment target

NCT02710162: Completed Early Phase 1 study, sponsored by University of Florida.

NCT02710162 is a Early Phase 1 study that has completed, run by University of Florida. The registered enrollment target is 21 participants, below the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (60% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02710162, a Early Phase 1 study, has completed, sponsored by University of Florida.

COMPLETED
Registry status
Early Phase 1
Development phase
21 participants
Enrollment target

Study Summary

Individuals with th Amyotrophic Lateral Sclerosis are at high risk for swallowing impairment (dysphagia) which leads to malnutrition, decreased pulmonary health, aspiration and aspiration pneumonia. These sequelae necessitate timely identification of at risk individuals to ensure optimal management of oral intake and pulmonary function. The purpose of this study is to evaluate the discriminant ability of several non-invasive screening tools at detecting swallowing impairment in individuals with ALS.

Interventions

  • DEVICE Electrical Impedance Myography
  • DRUG Capsaicin
  • PROCEDURE Videofluoroscopic Swallowing Study
  • DEVICE Iowa Oral Performance Instrument
  • DEVICE Micro Mouth Pressure Meter

Trial Details

FieldValue
Enrollment Target 21 participants
Start Date 2016-04
Est. Completion 2017-12-19
Phase Early Phase 1
University of Florida

1,106 total trials

What the finished NCT02710162 record still lists

NCT02710162 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 21 participants, a relatively small participant target, below the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (60% lower).

The record links to 0 conditions, and to 5 interventions - of which Electrical Impedance Myography is the first listed.

NCT02710162 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02710162 about?

NCT02710162 is a clinical study titled "Accurate Screening Tools for Dysphagia in Amyotrophic Lateral Sclerosis (ALS)". Individuals with th Amyotrophic Lateral Sclerosis are at high risk for swallowing impairment (dysphagia) which leads to malnutrition, decreased pulmonary health, aspiration and aspiration pneumonia. These sequelae necessitate timely identification of at risk individuals to ensure optimal management ...

What is the current status of trial NCT02710162?

This trial is currently completed. It is a Early Phase 1 study. The enrollment target is 21 participants. The study started on 2016-04. Estimated completion is 2017-12-19.

What interventions are being tested in trial NCT02710162?

The interventions under investigation include: Electrical Impedance Myography (DEVICE), Capsaicin (DRUG), Videofluoroscopic Swallowing Study (PROCEDURE), Iowa Oral Performance Instrument (DEVICE), Micro Mouth Pressure Meter (DEVICE).

Who is sponsoring clinical trial NCT02710162?

This trial is sponsored by University of Florida, which has 1,106 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02710162's enrollment target sits among peer trials

21 1130th of 2000 higher than 845 of 2,000 other Early Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Early Phase 1 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 enrollment target

  • NCT02447874 · 21 participants · Phase 1

    Arginine Therapy for the Treatment of Pain in Children With Sickle Cell Disease

  • NCT03826992 · 21 participants · Phase 1

    Venetoclax Combined With Vyxeos (CPX-351) for Participants With Relapsed or Refractory Acute Leukemia

  • NCT04107077 · 21 participants · Phase 2

    Phase II Study of the Effects of Laparoscopic Hyperthermic Intraperitoneal Chemotherapy (HIPEC) in Patients With Advanced Gastric Cancer

  • NCT04158635 · 21 participants · Phase 1

    Gemcitabine, Nab-Paclitaxel, and Bosentan for the Treatment of Unresectable Pancreatic Cancer

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02710162, the US trial registry maintained by the National Library of Medicine. NCT02710162 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.