NCT07649382

Brief Summary

We describe a single-center, retrospective case series (n = 10) for the utilization of dual instruments to extract foreign body at physiological narrowing. Foreign bodies that failed to remove with a single instrument or located in physiological narrowing into the duodenal bulb or descending duodenum were considered appropriate for this technique. Informed consent was obtained from all patients before the procedure.

Trial Health

75
On Track

Trial Health Score

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

Enrollment
10

participants targeted

Target at below P25 for all trials

Timeline
4mo left

Started Oct 2025

Geographic Reach
1 country

1 active site

Status
active not recruiting

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

Study Progress73%
Oct 2025Dec 2026

Study Start

First participant enrolled

October 1, 2025

Completed
8 months until next milestone

First Submitted

Initial submission to the registry

June 8, 2026

Completed
8 days until next milestone

First Posted

Study publicly available on registry

June 16, 2026

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2026

Expected
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2026

Last Updated

August 5, 2026

Status Verified

October 1, 2025

Enrollment Period

1 year

First QC Date

June 8, 2026

Last Update Submit

August 3, 2026

Conditions

Keywords

foreign body

Outcome Measures

Primary Outcomes (1)

  • Successful Endoscopic Foreign Body Removal Rate

    Percentage of patients in whom the foreign body is completely removed using the dual-instrument endoscopic retrieval technique without the need for surgical intervention. Success will be assessed by direct endoscopic visualization and procedural records.

    1 day

Secondary Outcomes (1)

  • Procedure-Related Adverse Event Rate

    1 week

Study Arms (1)

dual-instrument

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

In this study, we retrospectively examined the records of 10 patients who underwent endoscopic foreign body extraction at Zhongshan Hospital, Fudan University between January 2018 and January 2026. All patients initially presented to the emergency department and underwent an initial single-instrument endoscopic retrieval attempt. When single-instrument retrieval was unsuccessful or unstable, a dual-instrument endoscopic retrieval technique was subsequently applied. All procedures were performed by a single experienced therapeutic endoscopist.

You may qualify if:

  • Consecutive patients who underwent dual-instrument endoscopic retrieval for upper gastrointestinal foreign bodies at our center during the study period.

You may not qualify if:

  • Patients with incomplete clinical or procedural records. Patients lost to follow-up immediately after the procedure.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Zhongshan Hospital

Shanghai, China

Location

Related Publications (1)

  • 1. Yu S, Wang X, Chen X. Removal of giant spherical foreign body in the esophagus by double-forceps endoscope and double balloon. J Int Med Res. 2020;48(8):0300060520941332. doi:10.1177/0300060520941332 2. Birk M, Bauerfeind P, Deprez P, et al. Removal of foreign bodies in the upper gastrointestinal tract in adults: European society of gastrointestinal endoscopy (ESGE) clinical guideline. Endoscopy. 2016;48(05):489-496. doi:10.1055/s-0042-100456 3. Emara M, Darwiesh E, Refaey M, Galal S. Endoscopic removal of foreign bodies from the upper gastrointestinal tract: 5-year experience. CEG. Published online July 2014:249. doi:10.2147/CEG.S63274

    BACKGROUND

MeSH Terms

Conditions

Foreign Bodies

Condition Hierarchy (Ancestors)

Wounds and Injuries

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

June 8, 2026

First Posted

June 16, 2026

Study Start

October 1, 2025

Primary Completion (Estimated)

October 1, 2026

Study Completion (Estimated)

December 1, 2026

Last Updated

August 5, 2026

Record last verified: 2025-10

Data Sharing

IPD Sharing
Will not share

Locations