Esophageal Fully Covered Metal Stents in Caustic Strictures Study

Boston Scientific Corporation1 enrolled

Overview

The purpose of this study is to establish clinical proof of concept of temporary indwell of the WallFlex™ Esophageal Fully Covered Metal Stent (FCMS) for the treatment of refractory benign esophageal strictures caused by caustic ingestion. Also to collect data in support of a hypothesis required to prospectively document the safety and effectiveness of temporary indwell of the WallFlex™ Esophageal Fully Covered Metal Stent (FCMS) compared to repeated Bougie Dilation for the treatment of refractory benign esophageal strictures caused by caustic ingestion.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Refractory Benign Esophageal Strictures Caused by Caustic Ingestion

Interventions

Metal Stent (WallFlex™ Esophageal RX)DEVICE

Eligibility

Sex: ALLMin age: 18 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: 1. Availability of medical history pertaining to dysphagia score prior to and during the preceding SECSER. 2. Availability of patient history pertaining to weight prior to and at completion of SECSER. 3. Benign esophageal stricture caused by caustic ingestion 12 or more weeks prior to enrollment. 4. Single esophageal stricture or multiple esophageal stricture over a length \< 6 cm. 5. Having completed the SECSER consisting of 3 dilations intended to reach 15 mm each, separated by 2 weeks, followed by 3 dilations intended to reach 15 mm each with steroid injections, separated by 2 weeks. The dilations may be performed using Bougie or balloon dilation at the discretion of the investigator. 6. Refractory stricture defined as recurrence of stricture with associated dysphagia within 6 months after completion of SECSER. 7. Dysphagia score of 2 (ability to swallow semi-solid foods), 3 (ability to swallow liquids only) or 4 (unable to swallow liquids) at baseline. 8. Unable to pass a standard endoscope (approximately 9.8 mm diameter). 9. Age 18 years or older. 10. Willing and able to comply with the study procedures and provide written informed consent to participate in the study. Exclusion Criteria: 1. Stricture within 2 cm of the upper esophageal sphincter. 2. Concomitant Esophageal ulcerations. 3. Prior esophageal stent placements. 4. Concurrent gastric and/or duodenal obstruction. 5. Patients with prior full or partial gastrectomy. 6. Sensitivity to any components of the stent or delivery system. 7. Concurrent medical condition that would affect the investigator's ability to evaluate the patient's condition or could compromise patient safety. 8. Participation in a clinical trial evaluating an investigational device within 3 months prior to enrollment in this study.

Locations (2)

Postgraduate Institute of Medical Education and Research

Chandigarh, India

Asian Institute of Gastroenterology

Hyderabad, India

Outcomes

Primary Outcomes

Clinical Success

Clinical success consisting of stent tolerability and adequate ability to sustain nutrition to 6 months after stent removal. Stent tolerability defined as absence of pain-related stent removal. Adequate ability to sustain nutrition defined as absence of dysphagia-related reintervention.

Time frame: From stent placement on day 0 to 6 months after stent removal

Secondary Outcomes

Stent Placement Success

Number of participants with successful stent placement. Successful stent placement defined as the ability to deploy the stent in satisfactory position across the stricture

Time frame: Stent placement on Day 0

Stent Removal Success

Number of participants with successful stent removal. Successful stent removal defined as the ability to remove the stent endoscopically without serious stent removal related complications.

Time frame: Stent removal at Week 8 (±7 days)

Change in Patient's Report on Pain Compared to Baseline

Change in Patient's report on pain compared to Baseline at Day 2, Week 1, Week 2, Week 4, Week 6, and Thereafter every 2 weeks until stent removal at Week 8. Pain is reported on the VAS Pain Score scale from 0 (0 being No Pain) to 10 (10 being Worst Pain Ever). Higher score means a worse outcome. If reporting a score on a scale, please include the unabbreviated scale title, the minimum and maximum values, and whether higher scores mean a better or worse outcome.

Time frame: From baseline to stent removal at Week 8 (±7 days)

Change of Pain Medication Intake From Baseline

Change of pain medication intake from baseline at Day2, Week1, Week2, and thereafter every 2 weeks until stent removal

Time frame: From baseline to stent removal at Week 8 (±7 days)

Data from ClinicalTrials.gov

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Change in Dysphagia Score Compared to Baseline

Change in dysphagia score compared to Baseline at Day 2, Week 1, Week 2, Week 4, Week 6, Week 8, and thereafter every 2 weeks until end of study at Week 32. Change value was calculated as dysphagia score measured during stent treatment minus dysphagia score at Baseline. Dysphagia is reported using Dysphagia Scoring System (see scoring system below) with higher score meaning a worse outcome. 0 = ability to eat a normal diet 1. = ability to eat some solids 2. = ability to eat some semisolids only 3. = ability to swallow liquids only 4. = complete dysphagia

Time frame: From stent placement on day 0 to end of study at Week 32.

Dysphagia Score During Stent Treatment Compared to Score During Proceeding Standardized Esophageal Caustic Stricture Endoscopic Treatment Regimen (SECSER)

Change in Dysphagia score during stent treatment compared to dysphagia score during proceeding standardized esophageal caustic stricture endoscopic treatment regimen (SECSER). Change value was calculated as dysphagia score during stent treatment (Day 2, Week 1, Week 2, and thereafter every 2 weeks until end of study at Week 32 minus dysphagia score at SECSER. Dysphagia is reported using Dysphagia Scoring System (see scoring system below) with higher score meaning a worse outcome. 0\. = ability to eat a normal diet 1. = ability to eat some solids 2. = ability to eat some semisolids only 3. = ability to swallow liquids only 4. = complete dysphagia

Time frame: Dysphagia score at SECSER was measured prior to baseline. Dysphagia score during stent treatment was measured from stent placement on day 0 to end of study at Week 32

Change in Quality of Life (QOL) Compared to Baseline

Change in overall Quality of Life (QOL) health score compared to Baseline at Day 2, Week 1, Week 2, Week 4, Week 6, Week 8, and thereafter every 2 weeks until end of study at Week 32. QOL Overall Health Score is measured on a scale of 0 to 100, with 0 meaning the worst health you can imagine and 100 meaning the best health you can imagine. Higher score means a better outcome.

Time frame: From stent placement on Day 0 to end of study at Week 32

Occurrence of Adverse Events

Occurrence of Adverse Events Related to the Stent and/or the Stent Placement or Stent Removal Procedure and of All Serious Adverse Events Throughout the Duration of the Study