The study of looking for the optimal evaluation method of clinical activity by using new UC-Capsule Endoscopic Sore (UCCAS) LUCCAS study

The study of looking for the optimal evaluation method of clinical activity by using new UC-Capsule Endoscopic Sore (UCCAS) LUCCAS study - LUCCAS study

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000016156

Enrollment

Registered

2015-02-01

Start date

2015-02-01

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

Ulcerative colitis

Interventions

colonic capsule endoscopic examination

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: active UC patients with CAI more than 4 patients with written informed consent patients more than 18 and below 70 years old

Exclusion criteria

Exclusion criteria: patients with conformed or suspicious intestinal obstruction, stenosis or fistula patients with conformed and suspicious radiation colitis patients who will not be able to perform capsule endoscopy because of the history of abdominal surgery patients treated with operation of pacemaker and/or electric device patients with confirmed and suspicious swallowing disturbance patients with pregnancy and lactation patients with the treatment of malignancy papatients defined inappropriate for the entry into this study

Design outcomes

Primary

Measure	Time frame
correlation between UCCAS and CAI	—

Countries

Japan

Contacts

Public ContactShingo Kato

Saitama Medical Center, Saitama Medical University Department of Gastroenterology and Hepatology

skato@saitama-med.ac.jp049-228-3564

Outcome results

None listed

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