Using prior CT scans to guide colonoscope insertion

The Impact of Image-Assisted Colonoscope on Patient Experience, Physician Workload, and Examination Quality

Not applicable Interventional Peking Union Medical College Hospital · NCT07541924

This trial will test whether using a patient's existing abdominal/pelvic CT scan to guide colonoscope insertion makes colonoscopy faster and more comfortable for adults having screening or diagnostic colonoscopy.

Quick facts

PhaseNot applicable
Study typeInterventional
Enrollment200 (estimated)
Ages18 Years to 80 Years
SexAll
SponsorPeking Union Medical College Hospital Academic / other
Locations1 site (Beijing, Beijing Municipality)
Trial IDNCT07541924 on ClinicalTrials.gov

What this trial studies

This single-blind, randomized controlled trial at Peking Union Medical College Hospital will randomize 140 participants 1:1 to image-assisted insertion based on a prior abdominal/pelvic CT (≤5 years) or to standard insertion. The primary outcome is cecal intubation time, with secondary outcomes including patient-reported pain (VAS), willingness for future colonoscopy, operator workload (NASA-TLX), looping events, total procedure time, and polyp detection rate. Operators will record procedural findings and investigators will compare those findings with CT-based anatomical predictions to measure consistency and feasibility. The trial aims to provide prospective evidence on whether individualized, anatomy-informed insertion strategies improve examination quality and patient experience.

Who should consider this trial

Good fit: Adults aged 18–80 undergoing colonoscopy at Peking Union Medical College Hospital who have an abdominal/pelvic CT from within the past 5 years and no major abdominal surgery afterward are ideal candidates.

Not a fit: Patients without a usable CT within 5 years, those with prior colonic resections that alter anatomy, and those with severe cardiopulmonary dysfunction, coagulopathy, or pregnancy are unlikely to benefit or be eligible.

Why it matters

Potential benefit: If successful, this approach could shorten insertion time, reduce patient discomfort and operator workload, and improve overall exam quality and polyp detection.

How similar studies have performed: Retrospective CT-based analyses and fluoroscopy-guided maneuvers have suggested anatomical guidance can reduce looping and procedural difficulty, but prospective randomized evidence is currently lacking.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age 18-80 years, or expected natural survival \>3 years
* Undergoing colonoscopy at Peking Union Medical College Hospital
* Presence of an abdominal/pelvic CT scan performed within ≤5 years and no - - - major abdominal surgery afterward
* Patient or legal guardian able to understand the study and provide written consent

Exclusion Criteria:

* No available CT or CT quality insufficient for anatomical evaluation
* Prior colonic surgery affecting anatomy (e.g., right hemicolectomy, transverse colectomy)
* Severe cardiopulmonary dysfunction or coagulopathy
* Pregnancy
* Refusal to participate or inability to complete questionnaires
* Patient or guardian unable to understand study requirements

Where this trial is running

Beijing, Beijing Municipality

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions Colorectal Cancer ScreeningColonic Polyps/Colonoscopy/Colorectal NeoplasmsDifficult ColonoscopyColonoscopy-Related DiscomfortColonoscopyCecal Intubation TimeLoopingImage-Assisted Colonoscopy
Last reviewed 2026-06-09 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.