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Esophageal Stenosis clinical trials

View clinical trials related to Esophageal Stenosis.

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NCT ID: NCT04524897 Not yet recruiting - Clinical trials for Esophageal Stricture

The Use of Triamcinolone Injection in Treatment of Refractory Benign Esophageal Stricture in Children

Start date: December 1, 2020
Phase: Phase 4
Study type: Interventional

To evaluate the efficacy of Intra-lesional triamcinolone injection in the management of refractory benign esophageal Stricture in children.

NCT ID: NCT04372784 Not yet recruiting - Clinical trials for Esophageal Stricture

Cryoablation for Benign Gastrointestinal Anastomotic Strictures

Start date: September 2020
Phase: N/A
Study type: Interventional

Anastomotic stricture is a common complication following foregut surgery. The standard of care for these benign foregut anastomotic strictures is balloon dilatation. However, re-stenosis of strictures is also common, requiring frequent repetition of balloon dilatation. Cryotherapy is a novel therapy that may improve clinical outcomes following dilatation. The purpose of the present study is to conduct a randomized controlled trial to characterize the impact of cryotherapy on clinical outcomes and complications for benign anastomotic strictures following esophagectomy, gastrectomy, and bariatric surgery.

NCT ID: NCT04221867 Not yet recruiting - Clinical trials for Esophageal Stricture

Feasibility and Therapeutic Potential of Free Fat Grafts in the Treatment of Esophageal Strictures (ESOGRAFT)

ESOGRAFT
Start date: August 15, 2021
Phase: N/A
Study type: Interventional

In this study the investigators investigate the feasibility and therapeutic potential of free autologous fat grafting combined to dilation therapy in the treatment of benign esophageal strictures.

NCT ID: NCT03760354 Not yet recruiting - Esophageal Stenosis Clinical Trials

Corticosteroid Treatment in the Acute Phase of Caustic Ingestion Management

CORTICAU
Start date: February 15, 2019
Phase: Phase 2
Study type: Interventional

The management of patients who have ingested a caustic product has changed since 2007. Whereas previously the lesion assessment and surgical indication were based on endoscopic data, the therapeutic algorithm is currently based solely on the results of a CT scan with contrast injection, performed 6 hours after ingestion. This examination makes it possible to reliably assess the viability of the esophageal and gastric walls and thus to indicate digestive resection. The therapeutic consequences of this new treatment are important because, by expanding the indications for conservative treatment after severe ingestion, it brings a significant gain in terms of survival, morbidity and functional outcome. In the absence of emergency digestive resection, however, the functional prognosis is often overshadowed by the formation of esophageal stenosis in the months following ingestion. Patients then require endoscopic dilation treatment. In the event of failure or impossibility of dilation, which defines refractory stenosis, esophageal reconstruction is necessary. In case of sequential pharyngeal stenosis following ingestion, esophageal and pharyngeal reconstruction is indicated as a first-line treatment, since these stenosis do not respond to endoscopic dilations. The expansion of the indications for conservative treatment after severe ingestion using CT scans has led to an increase in the incidence of after-effect stenosis. We aim to develop a therapeutic approach that will prevent the development of refractory and pharyngeal esophageal stenosis. Indeed, there is currently no strategy that has proven effective in this regard in adults. The value of corticosteroid therapy for the prevention of caustic stenosis has only been evaluated in children and remains controversial. The main objective is to evaluate the effect of early systemic corticosteroid therapy on the risk of refractory esophageal or pharyngeal stenosis within one year of ingestion of a caustic substance in a population of patients at high risk of stenosis, defined according to tomodensitometric criteria (grade IIb: severe lesions, absence of transparietal necrosis), and for whom there is no indication of urgent digestive resection.

NCT ID: NCT03189927 Not yet recruiting - Clinical trials for Benign Esophageal Stricture

BD-Covered Stent for Benign Esophageal Strictures: a Safety and Feasibility Study

BIDARCA
Start date: July 1, 2017
Phase: N/A
Study type: Interventional

A non-randomized prospective clinical, pilot study in a single centre assessing the safety and feasibility of the esophageal biodegradable covered stent for refractory benign esophageal strictures with or without fistulae