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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT01958697
Other study ID # AG-BMI
Secondary ID
Status Active, not recruiting
Phase N/A
First received October 7, 2013
Last updated October 7, 2013
Start date July 2013
Est. completion date June 2014

Study information

Verified date October 2013
Source University Hospital, Gasthuisberg
Contact n/a
Is FDA regulated No
Health authority Belgium: Federal Agency for Medicines and Health Products, FAMHP
Study type Observational

Clinical Trial Summary

Esophagectomy for cancer is often accompanied with severe preoperative weight loss. Body Mass Index (BMI) values are age-independent and the same for both sexes. From the perspective that these two parameters should actually be taken into account too, we developed a model to calculate "age-gender specific BMI-percentiles" (AG-BMI) and tested this model in relation to survival outcome after esophagectomy for cancer.


Description:

Age-Gender specific BMI percentiles are more accurate compared to the current BMI classes in predicting Overall Survival (OS) after esophagectomy for cancer. Furthermore we believe in a more devastating impact on OS from underweight and not from overweight.

By preoperatively identifying risk patients for poorer OS, especially the non-tumoral deaths, this can be a tool to tailor postoperative nutritional strategies to counter further weight loss and bringing postoperative weight to normal ranges.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 650
Est. completion date June 2014
Est. primary completion date October 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 95 Years
Eligibility Inclusion Criteria:

- any type of esophagectomy

Exclusion Criteria:

- Preoperative organ metastasis (cM+ or yM+)

- esophageal bypass surgery

Study Design

Observational Model: Cohort, Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
Belgium Univresity Hospital Leuven - dept. Thoracic Surgery Leuven

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Gasthuisberg

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Overall 5 year survival Overall 5-year survival after esophagectomy for cancer 5 years after esophagectomy No
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