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NCT04159350 · ClinicalTrials.gov registry record · NA

Point-of-care Anorectal Testing to Predict Outcomes With Biofeedback Therapy: Clinical Trial

A NA study, sponsored by Dartmouth-Hitchcock Medical Center.

Completed
Registry status
NA
Development phase
99
Enrollment target

NCT04159350: Completed NA study, sponsored by Dartmouth-Hitchcock Medical Center.

NCT04159350 is a NA study that has completed, run by Dartmouth-Hitchcock Medical Center. The registered enrollment target is 99 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04159350, a NA study, has completed, sponsored by Dartmouth-Hitchcock Medical Center.

COMPLETED
Registry status
NA
Development phase
99 participants
Enrollment target

Study Summary

To prospectively evaluate the clinical utility of baseline anorectal function testing using a point-of-care device in predicting response of chronically constipated patients to physical therapy biofeedback training.

Primary Outcome

The Patient Assessment of Constipation-Symptoms (PAC-SYM) questionnaire is a short, easily-completed instrument for assessing global constipation symptoms. A total PAC-SYM score ranges from 0 to 48.

Interventions

  • DEVICE Rectal Expulsion Device (RED) - Feasibility
  • DEVICE Rectal Expulsion Device (RED) - Validation

Trial Details

FieldValue
Enrollment Target 99 participants
Start Date 2020-06-15
Est. Completion 2021-09-13
Phase NA
Dartmouth-Hitchcock Medical Center

427 total trials

What the finished NCT04159350 record still lists

NCT04159350 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 99 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower).

The record links to 0 conditions, and to 2 interventions - of which Rectal Expulsion Device (RED) - Feasibility is the first listed.

NCT04159350 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04159350 about?

NCT04159350 is a clinical study titled "Point-of-care Anorectal Testing to Predict Outcomes With Biofeedback Therapy: Clinical Trial". To prospectively evaluate the clinical utility of baseline anorectal function testing using a point-of-care device in predicting response of chronically constipated patients to physical therapy biofeedback training.

What is the current status of trial NCT04159350?

This trial is currently completed. It is a NA study. The enrollment target is 99 participants. The study started on 2020-06-15. Estimated completion is 2021-09-13.

What interventions are being tested in trial NCT04159350?

The interventions under investigation include: Rectal Expulsion Device (RED) - Feasibility (DEVICE), Rectal Expulsion Device (RED) - Validation (DEVICE).

Who is sponsoring clinical trial NCT04159350?

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

How this trial's enrollment target compares

Where NCT04159350's enrollment target sits among peer trials

99 920th of 2000 higher than 1,079 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 NCT04159350, the US trial registry maintained by the National Library of Medicine. NCT04159350 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.