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The study on efficacy and outcomes of treatment of mediastinum benign tumor by transesophageal endoscope

The study on efficacy and outcomes of treatment of mediastinum benign tumor by transesophageal endoscope

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000036447
Enrollment
Unknown
Registered
2020-08-23
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-09-14

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

Conditions

Mediastinal Tumor

Interventions

1:endoscopic surgery
2:thoracic surgery

Sponsors

Zhongshan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) Aged 18 to 75 years; 2) Patients with mediastinal benign tumor confirmed by CT imaging or endoscopic ultrasonography; 3) Those who can understand and accept the study protocol and sign informed consent voluntarily.

Exclusion criteria

Exclusion criteria: 1) Those who have no operation conditions or refuse to accept any operation; 2) Pregnant women; 3) Patients with dysphagia, known or suspected gastrointestinal obstruction, stenosis and fistula, obvious gastrointestinal bleeding, history of gastrointestinal surgery, or history of abdominal surgery and abdominal radiation that changed gastrointestinal anatomy; 4) Patients with contraindication of electronic gastroscope; 5) The researchers believe that there are other situations that are not suitable for this study; 6) Patients with pleural effusion and other malignant tumor indications.

Design outcomes

Primary

MeasureTime frame
complete tumor resection rate;

Secondary

MeasureTime frame
mediastinal organs and esophagus;improvement of symptoms;patient tolerance;long-term recurrence of tumor;survival of patients;satisfaction of patients;

Countries

China

Contacts

Public ContactGao Pingting

Zhongshan Hospital, Fudan University

gao.pingting@zs-hospital.sh.cn+86 13621908903

Outcome results

None listed

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