Predictive Model Identifies Painful Sedation-free Colonoscopy
A Predictive Model Identifies Patients Likely To Be Painful During Sedation-free Colonoscopy.
1 other identifier
observational
679
1 country
1
Brief Summary
Colorectal cancer is one of the most common cancers globally and a leading cause of cancer-related death. Colonoscopy is the standard screening method for colorectal cancer, significantly reducing mortality rates. However, the pain experienced during the procedure is one of the main reasons people avoid getting a colonoscopy. If operators can identify patients who are more likely to feel pain before the procedure, operators can take steps to reduce their discomfort. Previous research has developed a model to predict discomfort during colonoscopy, but this model have some limitations in clinical use. Therefore, investigators plan to develop a new model that also predicts the likelihood of painful colonoscopies. This study aims to identify factors related to pain in non-sedated colonoscopy and create a more accurate prediction model to help reduce pain during the procedure. A total of 679 patients will be divided into two groups randomly for training and validation. Participants meet the inclusion criteria for this study, and investigators will ask participants to participate voluntarily. If participants agree, investigators will collect some of participants basic information and medical history, and assess participants' pain during the procedure. Participants will only need to follow the doctors' instructions, complete bowel investigators' preparation, and undergo the colonoscopy as usual. The data collection will not interfere with participants' regular care
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Oct 2024
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 22, 2024
CompletedFirst Posted
Study publicly available on registry
October 10, 2024
CompletedStudy Start
First participant enrolled
October 10, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 21, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
September 21, 2025
CompletedNovember 24, 2025
September 1, 2025
12 months
September 22, 2024
November 19, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
colonoscopy-related pain
The primary outcome is the the pain during the procedure of sedated-free colonoscopy according to a 4-point verbal rating scale (VRS-4), which is a four-category lanuage scale that classifies pain as no(0), slight(1), moderate(2), and se vere(3).
during the intubation procedure of sedated-free colonoscopy
Eligibility Criteria
the people who is about to have a sedation-free colonoscopy
You may qualify if:
- Patients undergoing non-sedated colonoscopy at Ningbo University Affiliated Hospital from September 2024 to September 2025.
- Age: Patients aged 18 to 75 years.
- Voluntary participation: Patients who voluntarily agree to participate in the study and have signed the informed consent form.
You may not qualify if:
- Patients under 18 years old.
- Patients who are unwilling or unable to provide informed consent.
- Patients with malignant diseases, severe chronic heart or lung diseases, or those who have received treatment or radiation therapy for coronary artery or cerebrovascular events requiring hospitalization in the past 3 months.
- Patients with a history of colorectal resection or those with an incomplete colon.
- Patients who do not require reaching the ileocecal valve.
- Patients who have not completed bowel preparation or who have only used enemas for bowel cleaning.
- Patients with severe bowel obstruction or bowel perforation.
- Pregnant or breastfeeding women. -
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
the First Affiliated Hospital of Ningbo University, Ningbo
Ningbo, Zhejiang, 315000, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 22, 2024
First Posted
October 10, 2024
Study Start
October 10, 2024
Primary Completion
September 21, 2025
Study Completion
September 21, 2025
Last Updated
November 24, 2025
Record last verified: 2025-09