Effect of More Distal Enteral Bypass After Pancreaticoduodenectomy: A Prospective Multicenter Randomized Clinical Trial
NCT ID: NCT01755273
Last Updated: 2016-10-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
90 participants
INTERVENTIONAL
2013-01-31
Brief Summary
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Detailed Description
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In plan (to study if more distal bypass of gastrojejunostomy may increase remission of new-onset DM cases), the major concern of potential risk for patients participating the clinical trial is malnutrition due to enteral bypass. Other surgical procedures are the same as standard PD. For the monitoring of malnutrition, patients visited outpatient clinic every month for the first six months, and every three months afterward. The complete blood count and value of serum albumin will be checked very three months. The body weight loss \> 10% during three months is considered malnutrition. The peripheral parenteral nutrition will be administered to manage the malnutrition, and total parenteral nutrition should be used if malnutrition persisted. However, malnutrition is also a common phenomenon for recurrent cancer cases. The management of malnutrition for cancer patients will be managed according to clinical guidelines at National Taiwan University Hospital.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Standard pancreaticoduodenectomy
Cases receiving pancreaticoduodenectomy with standard enteral bypass
Pancreaticoduodenectomy with more distal enteral bypass
Patients undergoing pancreaticoduodenectomy, the enteral bypass (gastrojejunostomy/duodenojejunostomy is extra 100 cm away from standard bypass )
Interventions
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Pancreaticoduodenectomy with more distal enteral bypass
Patients undergoing pancreaticoduodenectomy, the enteral bypass (gastrojejunostomy/duodenojejunostomy is extra 100 cm away from standard bypass )
Eligibility Criteria
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Inclusion Criteria
* Patients with impaired fasting glucose before operation
Exclusion Criteria
* History of pancreatitis
* Hepatic dysfunction (Child-Pugh \> 2)
* Renal dysfunction (serum creatinine concentration \> 3 mg/L, hemodialysis, or both)
* Pregnancy
* Malnutrition (pre-operative BMI \<20)
20 Years
ALL
No
Sponsors
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National Taiwan University Hospital
OTHER
Responsible Party
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Principal Investigators
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Yu-Wen Tien, M.D. PhD
Role: PRINCIPAL_INVESTIGATOR
National Taiwan University Hospital
Locations
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National taiwan University Hospital
Taipei, Taipei, Taiwan
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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201203073RIC
Identifier Type: -
Identifier Source: org_study_id
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