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Clinical Trial Summary

Patients will be randomized into 2 groups:

- Group 60: Patients will undergo a Roux-en-Y gastric bypass with a Biliopancreatic limb length of 60cm

- Group 100: Patients will undergo a Roux-en-Y gastric bypass with a Biliopancreatic limb length of 100cm

Bone mineral density will be evaluated before surgery and 2 years after it.


Clinical Trial Description

Patients will be randomized into 2 groups:

- Group 60: Patients will undergo a Roux-en-Y gastric bypass with a Biliopancreatic limb length of 60cm

- Group 100: Patients will undergo a Roux-en-Y gastric bypass with a Biliopancreatic limb length of 100cm Alimentary limb will be constant in both groups (150cm length)

Bone mineral density will be evaluated before surgery and 2 years after it, by means of X ray absorptiometry (DEXA). Changes in bone mineral density in lumbar column will be assessed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04377230
Study type Interventional
Source Hospital General Universitario Elche
Contact Carolina LLavero Garrido
Phone 649593020
Email carolinallavero@gmail.com
Status Not yet recruiting
Phase Phase 3
Start date May 7, 2020
Completion date May 1, 2022

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