NCT06635941

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
679

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Oct 2024

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 22, 2024

Completed
18 days until next milestone

First Posted

Study publicly available on registry

October 10, 2024

Completed
Same day until next milestone

Study Start

First participant enrolled

October 10, 2024

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 21, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 21, 2025

Completed
Last Updated

November 24, 2025

Status Verified

September 1, 2025

Enrollment Period

12 months

First QC Date

September 22, 2024

Last Update Submit

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

Age18 Years - 80 Years
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

Location

MeSH Terms

Conditions

Pain

Condition Hierarchy (Ancestors)

Neurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

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

Locations