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Effect of Domperidone on Completion Rate of Vedio Capsule Endoscopy

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Fudan University

Status

Completed

Conditions

Pediatric Disorder
Capsule Endoscopy

Treatments

Dietary Supplement: water
Drug: Domperidone

Study type

Interventional

Funder types

Other

Identifiers

NCT03662113
DomperidoneVCE

Details and patient eligibility

About

Video capsule endoscopy (VCE) has become an established technique to investigate the presence of small bowel pathology. But the limited battery life of capsules can lead to incomplete small bowel visualization. There is a rationale to use prokinetic agents prior to VCE reduce the chances of an incomplete small bowel examination via decrease gastric transit time (GTT). Investigators are aimed to prospectively compare the completion rate of VCE in pediatric patients receiving prokinetic with those receiving no prokinetic.

Full description

Eligible children were randomly divided into two groups: domperidone prior to VCE and water prior to VCE. The primary outcome measure was the completion rate. Secondary outcome measures included the GTT and SBTT.

Enrollment

200 patients

Sex

All

Ages

3 to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Indications of capsule endoscopy;
  • Informed consent form obtained.

Exclusion criteria

  • Contraindication of capsule endoscopy;
  • Domperidone allergy;
  • Unwilling to participate.

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

200 participants in 2 patient groups

Experimental: Domperidone
Experimental group
Description:
5ml domperidone prior to VCE
Treatment:
Drug: Domperidone
Control: water
Other group
Description:
5ml warm water prior to VCE
Treatment:
Dietary Supplement: water

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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