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NCT01361750 Clinical Trial

The Effects of Gastric Tube on the Quality of Life and Nutritional Status After Ivor-Lewis Esophagectomy

Oesophageal Cancer Clinical Trial

Official title:
The Effects of Gastric Tube on the Quality of Life and Nutritional Status After Ivor-Lewis Esophagectomy: A Randomized Control Trial and Physiological Study

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT01361750
Other study ID # PKU-OES-001
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date May 2011
Est. completion date May 2012

Study information
Verified date March 2020
Source Peking University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is to investigate the effects of narrowed gastric tube on postoperative nutritional status and the quality of life in esophageal cancer patients treated with Ivor-Lewis esopagectomy in a 12-month follow-up period.

Recruitment information / eligibility
Status Terminated
Enrollment 21
Est. completion date May 2012
Est. primary completion date May 2012
Accepts healthy volunteers No
Gender All
Age group 30 Years to 75 Years
Eligibility Inclusion Criteria:

- esophageal cancer (squamous and adenocarcinoma subtypes)

- eligble for Ivor-Lowis esophagectomy

- expected survival time longer than 12 months

Exclusion Criteria:

- palliative resection(non-R0)

- anastomosis leak

- jejunum or colon transversum interponate

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• gastric tube
the stomach will be cut into a narrowed tube-shape conduit

Locations
Country Name City State
China Peking University School of Oncology Beijing Beijing

Sponsors (1)
Lead Sponsor Collaborator
Peking University

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary change of nutritional status and quality of life before and after operation before operation (baseline), 1 month, 6 month and 12 month after operation
Secondary change of serum markers and tissue inflammatory status before and after operation before operation (baseline), 1 month, 6 month and 12 month after operation
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