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Impact of 3D-planimetry on Optimized Therapeutic Assessment in Complex Benign Esophageal Stenosis

NCT07026357 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 22

Last updated 2025-06-18

No results posted yet for this study

Summary

Esophageal stenosis has a high impact on patients quality of live and food intake affecting personal nutrition status and general health.

For benign strictures of the esophagus, endoscopic dilatation therapy is recommended by actual guidelines.

Since the extent of dilatation is currently directed by endoscopic view and fluoroscopic imaging, patients are exposed to radiation and the determination of the appropriate extent of dilatation is difficult.

Therefore, the aim of this study is to compare the effect of 3D-planimetric measurement with current fluoroscopic monitoring on the success of endoscopic esophageal dilatation therapy in patients with benign esophageal stenosis.

Conditions

  • Benign Esophageal Stricture

Interventions

DEVICE

3D-planimetric measurement

Esophageal stenosis is evaluated by 3D-planimetric measurement

RADIATION

Fluoroscopic control

Fluoroscopic control of dilatation therapy

DIAGNOSTIC_TEST

Endoscopic control

Macroscopic endoscopic control of dilatation therapy

Sponsors & Collaborators

  • University Hospital Tuebingen

    collaborator OTHER

  • University Hospital Augsburg

    collaborator OTHER

  • University Hospital Munich

    collaborator OTHER

  • Thomas Seufferlein

    lead OTHER

Principal Investigators

  • Benjamin Walter, PhD · University Hospital Ulm

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-12-28
Primary Completion
2024-03-27
Completion
2024-03-27

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07026357 on ClinicalTrials.gov