Skip to main content
Clinical Trials/NL-OMON23356
NL-OMON23356
Completed
Not Applicable

Endoscopic Treatment of Anastomotic Esophageal Stricture. A Randomised Study Comparing Initial Dilation by Electrocautery with Savary Bougies with Electrocautery.

Address of correspondenceM.L. Hordijk, MDDepartment of Gastroenterology and HepatologyErasmus Medical Center Rotterdam University HospitalP.O. Box 20403000 CA RotterdamTel: + 31 010 4635946Email: m.hordijk@erasmusmc.nl0 sites62 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
English:Anastomotic Esophageal Stricture, Randomised Study, Electrocautery, Savary Bougies, dilatation. Nederlands: stenose anastomose oesophagus, elektrocoagulatie, Savary Bougies, Gerandomiseerde studie
Sponsor
Address of correspondenceM.L. Hordijk, MDDepartment of Gastroenterology and HepatologyErasmus Medical Center Rotterdam University HospitalP.O. Box 20403000 CA RotterdamTel: + 31 010 4635946Email: m.hordijk@erasmusmc.nl
Enrollment
62
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
Address of correspondenceM.L. Hordijk, MDDepartment of Gastroenterology and HepatologyErasmus Medical Center Rotterdam University HospitalP.O. Box 20403000 CA RotterdamTel: + 31 010 4635946Email: m.hordijk@erasmusmc.nl

Eligibility Criteria

Inclusion Criteria

  • Sixty\-two unselected consecutive patients with dysphagia due to a benign anastomotic stricture after transhiatal oesophagectomy with gastric tube reconstruction and cervical anastomosis will be included and randomized to either treatment arm. After informed consent, patients will either undergo dilation with Savary bougies, or primary electocautery.

Exclusion Criteria

  • 1\. Esophageal dilation with bougies or electrocautery is rarely contraindicated.
  • Patients should however not be dilated if they recently suffered from acute esophageal perforation.

Outcomes

Primary Outcomes

Not specified

Similar Trials