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

C

Canisius-Wilhelmina Hospital

Status and phase

Completed
Phase 4

Conditions

Pancreatitis

Treatments

Drug: Erythromycin
Drug: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT00999232
Bengmark_v1

Details and patient eligibility

About

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.

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

0 participants in 2 patient groups, including a placebo group

Erythromycin
Experimental group
Treatment:
Drug: Erythromycin
Placebo
Placebo Comparator group
Treatment:
Drug: Placebo

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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