NCT07772648

Brief Summary

The main questions it aims to answer are: Does starting colonoscopy in the supine position compared with the left lateral position affect the time required to reach the cecum? Does the starting position affect endoscopist comfort, patient comfort, procedure duration, polyp and adenoma detection, or the need to change the patient's position during the procedure? Participants will be randomly assigned to undergo colonoscopy starting either in the supine position or in the left lateral position. The colonoscopy will otherwise be performed according to standard clinical practice.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
158

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Mar 2025

Shorter than P25 for not_applicable

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

Study Start

First participant enrolled

March 1, 2025

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 31, 2025

Completed
8 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 5, 2025

Completed
8 months until next milestone

First Submitted

Initial submission to the registry

August 13, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

August 19, 2026

Completed
Last Updated

August 19, 2026

Status Verified

November 1, 2024

Enrollment Period

1 month

First QC Date

August 13, 2026

Last Update Submit

August 18, 2026

Conditions

Keywords

Endoscopist ergonomicsCecal intubation timePatient positioning

Outcome Measures

Primary Outcomes (2)

  • Endoscopist Comfort Score (ECS)

    Endoscopist comfort was assessed using a 100-mm visual analog scale (VAS), converted to a 0-10 numeric score, with higher scores indicating greater comfort.

    Immediately after completion of the colonoscopy

  • Patient Comfort Score (PCS)

    Patient comfort was assessed using a 100-mm visual analog scale (VAS), converted to a 0-10 numeric score, with higher scores indicating greater comfort.

    After recovery from anesthesia on the day of the colonoscopy

Secondary Outcomes (7)

  • Cecal Intubation Time (CIT)

    During the colonoscopy, from colonoscope insertion to cecal intubation

  • Withdrawal Time (WT)

    During the colonoscopy

  • Adenoma Detection Rate (ADR)

    Up to 30 days after colonoscopy

  • Polyp Detection Rate (PDR)

    During the colonoscopy

  • Requirement for Patient Repositioning

    During the colonoscopy

  • +2 more secondary outcomes

Study Arms (2)

Supine Position

EXPERIMENTAL

Participants assigned to this arm underwent colonoscopy starting in the supine position.

Procedure: Colonoscopy Starting Position

Left Lateral Position

ACTIVE COMPARATOR

Participants assigned to this arm underwent colonoscopy starting in the left lateral position

Procedure: Colonoscopy Starting Position

Interventions

Participants were assigned to undergo colonoscopy starting either in the supine position or in the left lateral position according to randomization. The assigned position was used at the beginning of the procedure. Patient repositioning during colonoscopy was permitted when clinically required to facilitate colonoscope advancement or completion of the procedure.

Left Lateral PositionSupine Position

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Adults aged 18 years or older. Scheduled to undergo screening colonoscopy. No history of colorectal cancer. No history of colorectal surgery.

You may not qualify if:

  • Failure to achieve cecal intubation. Inflammatory bowel disease. Inadequate bowel preparation, defined as a Boston Bowel Preparation Scale (BBPS) score \<2.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Şişli Hamidiye Etfal Training and Research Hospital

Istanbul, Istanbul, 34371, Turkey (Türkiye)

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
General Surgeon, MD

Study Record Dates

First Submitted

August 13, 2026

First Posted

August 19, 2026

Study Start

March 1, 2025

Primary Completion

March 31, 2025

Study Completion

December 5, 2025

Last Updated

August 19, 2026

Record last verified: 2024-11

Data Sharing

IPD Sharing
Will not share

There is no current plan to share individual participant data (IPD).

Locations