Impact of Indigo Carmine Pump Spraying on the Adenoma Detection Rate

Not Applicable

Completed

• Conditions: Colonic Polyps; Adenomatous Polyps; Adenoma Detection Rate; Chromoendoscopy; Colorectal Neoplasms
• Interventions: Procedure: Chromoendoscopy; Procedure: Conventional colonoscopy

• Registration Number: NCT06596317
• Lead Sponsor: Shandong University

Brief Summary

Detection and removal of polyps during colonoscopy is crucial for the prevention of colorectal cancer. Indigo carmine spraying up to the colonic mucosa could probably increase the adenoma detection rate. The traditional method of dye spraying with spraying catheter or syringe would consume a lot of time and dye volume. Now, the more convenient auxiliary water supply channel can be used to spray indigo carmine. In order to explore the clinical application value of spraying indigo carmine solution by auxiliary water channel in high-risk population, we performed a prospective, randomized controlled trial to compare adenoma detection rate of conventional colonoscopy and chromoendoscopy.

Detailed Description

If patients scheduled for colonoscopy meet the inclusion criteria but not the exclusion criteria, he or she will be recruited to the study and randomized to one of two groups. Subjects in Group A (treatment group) will undergo colonoscopy with spraying indigo carmine solution during withdrawal process. Subjects in Group B (control group) will undergo a standard conventional colonoscopy without spraying any solution during withdrawal process. The traditional method of dye spraying with spraying catheter or syringe would consume a lot of time and dye volume. The solution spraying process was implemented by a water jet channel using auxiliary foot pump. Any lesions found during the procedure will be removed and sent for pathological examination. The investigator will record the patient's general information (such as gender, age, symptoms, body mass index， etc.), colonoscopy data (such as duration, dye amount, etc.), and lesion characteristics (such as location, morphology, histopathological classification, etc.). Randomization was done with SPSS program. All data were analyzed according to the ITT analysis, and the PP analysis was performed for all outcomes. Continuous variables were presented as means ± standard deviation (SD), and compared using the Student t test. Categorical data were expressed as number with percentage and analyzed using the chi-squared test or the Fisher exact test. All statistical analyses were performed using IBM SPSS Statistics or R Statistics, and 2-sided P\<0.05 was statistically significant.

Study Timeline

• Study First Submitted: 2023-04-12
• Study Start: 2024-01-11
• Study First Submitted QC: 2024-09-10
• Study First Posted: 2024-09-19
• Primary Completion: 2024-12-30
• Study Completion: 2024-12-30
• Status Verified: 2025-03
• Last Update Submitted: 2025-03-11
• Last Update Posted: 2025-03-12

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 330

Inclusion Criteria

• Patients with a history of colorectal cancer or colorectal adenoma
• Patients whose first-degree relatives have a history of colorectal cancer or colorectal adenoma
• Patients with gastrointestinal symptoms (abdominal pain, bloody stool, chronic diarrhea or constipation, Unexplained anemia or weight loss;
• Patients with positive fecal occult blood tests

Exclusion Criteria

• Patients with severe comorbidity
• Patients who are not suitable for colonoscopy
• Patients who received urgent or therapeutic colonoscopy
• Patients with pregnancy, inflammatory bowel disease, polyposis syndromes, suspected CRC; intestinal obstruction, coagulopathy
• Patients with aspirin, clopidogrel or other anticoagulants/ antiplatelet drugs intake within 7 days
• Patients with failed cecal intubation
• Patients with inadequate bowel preparation quality (Boston score ≤5)
• Patients who refuse to participate or to provide informed consent

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Chromoendoscopy with indigo carmine solution spray	Chromoendoscopy	Patients in this group will be carefully observed with spraying indigo carmine solution during the colonoscopy withdraw.
Conventional colonoscopy without indigo carmine solution spray	Conventional colonoscopy	Patients in this group will be carefully observed without spraying anything during the colonoscopy withdraw.

Primary Outcome Measures

Name	Time	Method
adenoma detection rate(ADR)	procedure time	ADR was calculated as the number of patients with at least one adenoma divided by the total number of patients. In other words, the adenoma detection rate of the sample was the proportion of patients with adenoma detected.

Secondary Outcome Measures

Name	Time	Method
detected rate of different lesions	procedure time	Lesions are classified according to their size, location, morphology and histopathology, the corresponding detection rate was calculated as secondary outcome measures.

Trial Locations

Locations (1)

Qilu Hospital of Shandong University; 🇨🇳 Jinan, Shandong, China