Use of Metal Stents on Benign Esophageal Lesions

Prospective Evaluation of the Clinical Utility of the Endoscopic Placement of Mental Stent for Benign Esophageal Lesions

Status

Withdrawn

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01238913

Enrollment

Registered

2010-11-11

Start date

2015-09-30

Completion date

2015-09-30

Last updated

2015-10-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Benign Esophageal Lesions

Brief summary

The evaluation of using metal stents as medically indicated for the treatment of benign esophageal lesions.

Interventions

PROCEDUREEndoscopy

Endoscopic placement of an esophageal metal stent as per medical indication.

Study design

Observational model

CASE_ONLY

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

1. Subject is 18 years or older 2. Subject has medical indication to undergo endoscopic placement of esophageal metal stent 3. Subject must be able to give informed consent

Exclusion criteria

1. Any contraindications for endoscopic placement of esophageal metal stent 2. The subject is unable to give informed consent.

Design outcomes

Primary

Measure	Time frame	Description
Successful stenting of Benign esophageal lesions	approximately 2-3 hours	This is an observational study to determine the effectiveness of stenting benign esophageal lesions with a metal stent.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026