Evaluation of a new preparation regimen in colon capsule endoscopy

Evaluation of a new preparation regimen in colon capsule endoscopy - A new preparation regimen in colon capsule endoscopy

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000024073

Enrollment

Registered

2016-09-20

Start date

2016-10-01

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asymptomatic volunteer

Interventions

Standard preparation regimen in Europe New preparation regimen

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Volunteers who are able to write a consent form

Exclusion criteria

Exclusion criteria: 1. Subjects who have dysphagia or aspiration pneumonia 2. Subjects who have history of surgery in gastrointestinal tract 3. Subjects who may have gastrointestinal obstruction 4. Subjects who have toxic megacolon 5. Subjects who have hypertension or renal failure 6. Subjects who have congestive heart failure or unstable angina 7. Subjects who have long QT syndrome or serious arrythmia 8. Subjects who have ascites 9. Subjects who have electrolyte imbalance 10. Subjects who have delayed gastric emptying 11. Subjects who have pacemaker or implantable cardioverter-defibrillator 12. Subjects who have allergy for drugs and foods used in the study 13. Subjects who are pregnant and who are breast-feeding 14. Subjects who are not suitable for the study

Design outcomes

Primary

Measure	Time frame
capsule excretion rate	—

Secondary

Measure	Time frame
feelings during and after prepation	—

Countries

Japan

Contacts

Public ContactShiko Kuribayashi

Gunma University Hospital Department of Gastroenterology and Hepatology

shikokuri@gunma-u.ac.jp0272208137

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026