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NCT01156129 · ClinicalTrials.gov registry record · Phase 1

Interventions to Decrease the Impact of Post-OPerative Ileus After Liver Transplant or Resection Surgery

A Phase 1 study, sponsored by University of Nebraska.

Completed
Registry status
Phase 1
Development phase
111
Enrollment target

NCT01156129 is a Phase 1 study that has completed, run by University of Nebraska. The registered enrollment target is 111 participants.

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The verdict

NCT01156129, a Phase 1 study, has completed, sponsored by University of Nebraska.

COMPLETED
Registry status
Phase 1
Development phase
111 participants
Enrollment target

Study Summary

This is a randomized controlled trial to assess ways to address post-operative ileus (POI) in adult patients on the liver transplant service undergoing either liver transplant or resection surgery. Patient who speak and understand English will be randomized into one of three groups including a.)control group receiving standard therapy for post-operative ileus, b.)group receiving standard therapy and acupressure bracelets, and c.)group receiving standard therapy and sugar free gum four times daily.

Interventions

  • DRUG stool softener
  • DEVICE Arm B: Acupressure bracelet
  • DIETARY_SUPPLEMENT sugar free gum

Trial Details

FieldValue
Enrollment Target 111 participants
Start Date 2010-09-01
Est. Completion 2012-12-01
Phase Phase 1

Sponsor

University of Nebraska

407 total trials

What the Registry Record Tells You About NCT01156129

The ClinicalTrials.gov registry entry for NCT01156129 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 111 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Nebraska, which has 407 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which stool softener is the first listed.

NCT01156129 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01156129 about?

NCT01156129 is a clinical study titled "Interventions to Decrease the Impact of Post-OPerative Ileus After Liver Transplant or Resection Surgery". This is a randomized controlled trial to assess ways to address post-operative ileus (POI) in adult patients on the liver transplant service undergoing either liver transplant or resection surgery. Patient who speak and understand English will be randomized into one of three groups including a.)cont...

What is the current status of trial NCT01156129?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 111 participants. The study started on 2010-09-01. Estimated completion is 2012-12-01.

What interventions are being tested in trial NCT01156129?

The interventions under investigation include: stool softener (DRUG), Arm B: Acupressure bracelet (DEVICE), sugar free gum (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT01156129?

This trial is sponsored by University of Nebraska, which has 407 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.