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Evaluating Location of Biopsy Procurement in Active Crohn*s Disease

Evaluating Location of Biopsy Procurement in Active Crohn*s Disease - RP1602

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON43265
Enrollment
20
Registered
2016-08-29
Start date
2016-09-14
Completion date
Unknown
Last updated
2024-04-23

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

Conditions

Crohn's Disease inflammatory bowel disease

Interventions

None listed

Sponsors

Robarts Clinical Trials BV
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: (1) Male or females, 18 years of age or older. (2) Histologically confirmed Crohn*s disease (L1, L2 or L3) prior to study ileo-colonoscopy (3) Not on systemic anticoagulation therapy including warfarin or novel oral anticoagulants (4) Ability of subject to participate fully in all aspects of this clinical trial. (5) Written informed consent must be obtained and documented. (6) A single ulcer > 0.5 cm at study ileo-colonoscopy

Exclusion criteria

Exclusion criteria: Pregnant Women

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)