An interventional study of Savary bougie dilation in Benign Esophageal Stricture, sponsored by Radboud University Medical Center. Status unknown at 1 site in Netherlands. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2017-06-19.
Sponsored by Radboud University Medical Center · Not applicable, Interventional, and Treatment
A randomized controlled prospective clinical trial assessing the efficacy and safety of progressive esophageal dilation compared to conservative esophageal dilation in patients with severe benign esophageal strictures.
A randomized controlled prospective clinical trial assessing the efficacy and safety of progressive esophageal dilation (up to 6mm) compared to esophageal dilation according to the rule-of-3 in patients with severe benign esophageal strictures. Patients will be followed up for 6 months. When recurrent dysphagia occurs within 6 months the patients will be dilated according to the previously allocated strategy.
50 studies on the registry are indexed under Esophageal Stenosis; 11 are open to participants now.
This study's planned enrollment of 80 is above the median of 24 across 41 interventional studies indexed under Esophageal Stenosis.
Browse Esophageal Stenosis studies →Radboud University Medical Center is the lead sponsor of 959 studies on the registry; 134 are open to participants now.
Of its 6 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
Endoscopic exclusion criteria:
Patients will be dilated \> 3mm and can be dilated up to 6mm in diameter
Device: Savary bougie dilation
Patients will be dilated according to the rule-of-3 (i.e. dilation of no more than 3mm in diameter)
Device: Savary bougie dilation
Patients will be dilated with the use of the Savary bougienage device
Total number of dilation procedures within 6 months of follow-up
Total number of dilation procedures within 6 months of follow-up
Time frame: 6 months
Total number of dilation procedures during first dilation session to 16-18mm
Total number of dilation procedures during first dilation session to 16-18mm
Time frame: 1 month
Dysphagia free patients
Number of patients remaining dysphagia free within 6 months after dilation to 16-18mm
Time frame: 6 months
Timeframe first dilation session
Time from first dilation session to dilation of 16-18mm
Time frame: 1 month
Dysphagia free time period
Time to dilation of recurrent stricture after initial dilation to 16-18mm
Time frame: 6 months
Incidence of treatment-related mortality (serious) adverse events (safety)
Incidence of treatment-related mortality (serious) adverse events (safety)
Time frame: 7 months
Quality of Life
SF-36, disease specific questionnaire
Time frame: 6 months
Medical costs
Direct medicals costs: procedures, secondary interventions
Time frame: 7 months
Plan to share: No
No publications or documents are linked to this record.
This study is status unknown, as verified in May 2017. You cannot join it, but the record below documents what was studied.
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Radboud University Medical Center