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Assess the Effect of Erythromycin on the Rate of Success in Placement of a Self-propelled Feeding Tube

Information source: Canisius-Wilhelmina Hospital
ClinicalTrials.gov processed this data on August 23, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Pancreatitis

Intervention: Erythromycin (Drug); Placebo (Drug)

Phase: Phase 4

Status: Completed

Sponsored by: Canisius-Wilhelmina Hospital

Summary

The purpose of this study is to assess the effect of erythromycin on the Rate of Success in Placement of a Self-propelled Feeding Tube.

Clinical Details

Study design: Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Primary outcome: The success rate of spontaneous positioning the tubes tip into the jejunum, beyond Treitz ligament, after 48 hours.

Secondary outcome:

The success rate of spontaneous positioning the tubes tip into the jejunum, beyond Treitz ligament, after 24 hours.

Adverse events using this self-propelled tube

Eligibility

Minimum age: 18 Years. Maximum age: 80 Years. Gender(s): Both.

Criteria:

Inclusion Criteria:

- Aged 18-80 years

- Having pancreatitis

- Require jejunal enteral nutrition

Exclusion Criteria:

- Known impaired peristalsis (critically ill patients, postoperative patients, history

of surgery of the stomach/duodenum)

- Pregnancy

- Hypersensibility to erythromycin

- Cardiac arrhythmias with a prolonged QT-time

- Simultaneous usage of drugs impairing peristalsis

Locations and Contacts

Additional Information

Starting date: October 2004
Last updated: January 21, 2010

Page last updated: August 23, 2015

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