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Balloon catheter combination with APC and Savary bougienage via endoscopy for the treatment of Intractable anastomotic-stenosis after esophageal squamous cancer surgery

Balloon catheter combination with APC and Savary bougienage via endoscopy for the treatment of Intractable anastomotic-stenosis after esophageal squamous cancer surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-14004394
Enrollment
Unknown
Registered
2014-03-14
Start date
2014-03-18
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Esophygeas Cancer

Interventions

self-serve dilation group:Balloon catheter combination with APC and Savary bougienage via endoscopy
control:APC and Savary bougienage

Sponsors

1th Affiliated Hospital of Henan Univercity of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: Age 40-80 years old, written consent to participate in the study, undergone a transhiatal esophagectomy and intrathoracic gastric tube reconstruction with cervical anastomosis because of esophageal squamous cancer, III or IV degree of dysphagia, interval between treatment of stenosis and the initial surgery of esophageal cancer is less than 1 year, dysphagia recurrence after 1 time dilation by APC combination with SB at least within 3 months.

Exclusion criteria

Exclusion criteria: Anastomotic-stenosis caused by anastomotic recurrence of cancer and polyps, undergone APC or any form of re-canalization in the previous 30 days Karnofsky status < 40%, presenting with an esophageal fistula or with infiltration on the trachea or main bronchi on computed tomography.

Design outcomes

Primary

MeasureTime frame
dysphagia-free time;

Countries

China

Contacts

Public ContactShegan GAO

1st Affiliated Hospital, Henan Univercity of Science and Technology

gsg112258@163.com+86 18638859977

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026