Three different limited bowel preparation regimes for CT colonography: evaluation of image quality and patient acceptance

Three different limited bowel preparation regimes for CT colonography: evaluation of image quality and patient acceptance - CTC tagging study

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON32386

Enrollment

Registered

2008-09-15

Start date

2008-10-01

Completion date

Unknown

Last updated

2024-05-06

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

Conditions

colorectal carcinoma colorectal polyps

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: All patients who are tested positive in the framework of the ZONMW granted FOBT pilot study, who are willing to undergo colonoscopy and who want to give informed consent.

Exclusion criteria

Exclusion criteria: Patients who had examinations for research purposes with radiation exposure in the last 12 months, iodine contrast allergy, hyperthyroidism and pregnancy.

Design outcomes

Primary

Measure	Time frame
The main study endpoints are the homogeneity and density of the residual faeces, the amount of residual fluid and the quality of tagging in CTC*s and the patient acceptance in three patient groups that received different iodine tagging preparations.	—

Secondary

Measure	Time frame
Secondary endpoint is evaluation of the polyp detection in the three patient groups that received a different bowel preparation.	—

Countries

Netherlands

Outcome results