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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01528059
Other study ID # DongFang
Secondary ID FNSP2009Y0039
Status Recruiting
Phase Phase 2/Phase 3
First received February 2, 2012
Last updated February 6, 2012
Start date February 2012
Est. completion date March 2013

Study information

Verified date February 2012
Source Xiamen University
Contact Yu Wang, M.D
Phone 13805019453
Email flyfishwang@hotmail.com
Is FDA regulated No
Health authority China: Ministry of Health
Study type Interventional

Clinical Trial Summary

Gastric bypass improves glycemic levels in type 2 diabetes. However, the efficacy may be varied by different gastric-small intestine reconstruction used in the procedure. There are reports that Roux en Y reconstruction may give a better result. The purpose of this study is to compare Roux en Y and Billroth II reconstruction in patients with gastric cancer comorbid with type 2 diabetes.


Description:

Type 2 diabetes may cause severe complications such as nephropathy and retinopathy. Additionally, it is associated with increased risk for cardiovascular events and diseases. Surgical intervention with gastric bypass has been shown to attenuate glycemic levels in obese patient comorbid with type 2 diabetes. However, since gastric bypass is not a standard procedure, surgical protocol including stomach and small intestine reconstruction may be varied. The investigators and others have found that stomach and small intestine reconstruction may affect the efficacy of diabetic treatment. In this study, the investigators will compare the efficacy of Billroth II and Roux en Y reconstruction on glycemic control in stomach cancer patients with type 2 diabetes. Both Billroth II and Roux en Y are used in stomach-small intestine reconstruction after subtotal gastrectomy. No differences in postoperative outcomes and quality of life have been reported in Billroth II and Roux en Y reconstruction.


Recruitment information / eligibility

Status Recruiting
Enrollment 110
Est. completion date March 2013
Est. primary completion date February 2012
Accepts healthy volunteers No
Gender Both
Age group 30 Years to 70 Years
Eligibility Inclusion Criteria:

1. Diagnosed with Type 2 diabetes

2. Diagnosed with gastric cancer

Exclusion Criteria:

1. Type 1 diabetes

2. Unresectable cancers

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Intervention

Procedure:
Stomach-small intestine reconstruction
Billroth II or Roux en Y reconstruction will be performed after gastric resection in stomach patients co-morbid with type 2 diabetes

Locations

Country Name City State
China DongFang Hospital Fuzhou Fujian

Sponsors (1)

Lead Sponsor Collaborator
feng Zheng

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Glycemic control Fasting and postprandial glycemic levels, HbA1C
Number of anti-diabetic drugs
Dosage of anti-diabetic drugs
1 year after surgery No
Secondary Nutritional status assessment Body mass index
Anthropometric analysis
Plasma concentrations of albumin, pre-albumin, transferrin,and CRP
1 year after surgery No
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