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RECRUITING NA

Early Versus Late Endoscopic Stenting for Refractory Benign Esophageal Strictures

NCT06991049 · View on ClinicalTrials.gov ↗

Study Summary

This project is being done to compare two current treatment clinical options for management of RBES: 1) Frequent dilations followed by temporary esophageal stent placement if dilations fail, or 2) Early stent placement followed by dilations

Interventions

  • DEVICE Fully covered self-expandable metal esophageal stent

Study Locations (1)

Wisconsin

  • Froedtert Hospital — Milwaukee

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2025-10-14
Est. Completion 2027-07
Phase NA

Sponsor

Medical College of Wisconsin

614 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06991049

The ClinicalTrials.gov registry entry for NCT06991049 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Medical College of Wisconsin, which has 614 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Refractory Benign Esophageal Strictures appearing as the primary indexed condition, and to 1 intervention — of which Fully covered self-expandable metal esophageal stent is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06991049 reports 1 study location spanning 1 distinct geographic area — top geographies include Wisconsin. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06991049 about?

NCT06991049 is a clinical study titled "Early Versus Late Endoscopic Stenting for Refractory Benign Esophageal Strictures". This project is being done to compare two current treatment clinical options for management of RBES: 1) Frequent dilations followed by temporary esophageal stent placement if dilations fail, or 2) Early stent placement followed by dilations

What is the current status of trial NCT06991049?

This trial is currently recruiting. It is a NA study. The enrollment target is 20 participants. The study started on 2025-10-14. Estimated completion is 2027-07.

What conditions does trial NCT06991049 study?

This clinical trial studies the following conditions: Refractory Benign Esophageal Strictures. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06991049?

The interventions under investigation include: Fully covered self-expandable metal esophageal stent (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06991049?

This trial is sponsored by Medical College of Wisconsin, which has 614 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06991049 being conducted?

This trial has 1 study location across Wisconsin. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial