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Proximal Roux-en-y Gastrojejunal Anastomosis on Delayed Gastric Emptying After Pylorus-resecting Pancreaticoduodenectomy

Proximal Roux-en-y Gastrojejunal Anastomosis on Delayed Gastric Emptying After Pylorus-resecting Pancreaticoduodenectomy: A Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02954302
Enrollment
140
Registered
2016-11-03
Start date
2016-09-30
Completion date
2018-12-31
Last updated
2016-11-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bile Duct Cancer, Duodenal Cancer, Pancreatic Cancer

Keywords

Delayed gastric emptying, pancreaticoduodenectomy

Brief summary

This study aims to evaluate whether the incidence of delayed gastric emptying (DGE) can be reduced by proximal Roux-en-y gastrojejunal anastomosis in comparison with the standard gastrojejunal anastomosis in pylorus-resecting pancreaticoduodenectomy (PrPD).

Detailed description

Delayed gastric emptying (DGE) is a common complication after pancreaticoduodenectomy (PD), occurring in 20% to 70% of the patients. DGE is usually not a life-threatening complication, but it contributes significantly to increased length of hospital stay, health care costs, and patient discomfort. In a recent study by Sakamoto et al, proximal Roux-en-y gastrojejunal anastomosis is associated with a reduced incidence of DGE after pylorus-resecting pancreaticoduodenectomy (PrPD); however, these results may have been biased because of the retrospective nature. Therefore, the investigators conducted the present randomized controlled trial (RCT) to evaluate the impact of the proximal Roux-en-y gastrojejunal anastomosis on reducing DGE following PrPD.

Interventions

PROCEDUREPrPD with proximal Roux-en-y gastrojejunal anastomosis

the distal antrum was divided about 1 to 2 cm proximal to the pylorus ring, preserving more than 95% of the stomach. The proximal jejunum was divided approximately 2 to 4 cm distal to the duodeno-jejunal junction. After completion of the resection, the proximal end of the first loop of jejunum was then brought through the transverse mesocolon, and the gastrojejunal anastomosis (GJA) was performed in two layers by using 3-0 PDS sutures and 4-0 silk sutures in an end-to-side fashion. The jejunum was then divided 35 to 40 cm distal to the GJA, and the distal limb was brought separately through the transverse mesocolon to be placed in the duodenal bed for reconstruction of the pancreatojejunal anastomosis (PJA) and hepatojejunal anastomosis (HJA).

PROCEDUREconventional PrPD

After completion of the pancreatojejunal anastomosis (PJA) and hepatojejunal anastomosis (HJA), a hand-sewn, isoperistaltic GJA was performed 25 to 30 cm distal to the HJA in two layers by using 3-0 polydioxanone (PDS) sutures and 4-0 silk sutures.

Sponsors

LanZhou University
CollaboratorOTHER
Eastern Hepatobiliary Surgery Hospital
CollaboratorOTHER
The First Affiliated Hospital of Xiamen University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients who were scheduled to undergo PD and provided written informed consent. * In the opinion of the surgeon, the subject has no medical contraindications to PD. * At least 18 years of age.

Exclusion criteria

* Patients who underwent other surgical procedures than PD, such as total pancreatectomy (TP) or a palliative biliary and gastroenteric anastomosis. * Drug abusers or alcoholics. * Patient who have previous transabdominal surgery. * The patient who were scheduled to undergo laparoscopic PD. * The patient who does not want to participate the clinical trials.

Design outcomes

Primary

MeasureTime frameDescription
Delayed gastric emptying,rate60 days after operationThe severity of DGE was classified into 3 grades (A, B, or C) according to the ISGPS's clinical criteria, based on the patient's clinical course and postoperative management, such as the need for NGT in the postoperative period or the inability to tolerate solid oral intake. Grade A was defined as needing the NGT for more than 7 days or reinsertion of the NGT after postoperative day 3, or as being unable to tolerate a solid diet by postoperative day 7. Grade B was defined as needing for NGT for 8 to 14 days after surgery or reinsertion of the NGT after day 7, or as being unable to tolerate a solid diet by postoperative day 14. Grade C was defined as needing the NGT for more than 14 days or reinsertion of the NGT after day 14, or as being unable to tolerate a solid diet by day 21.

Secondary

MeasureTime frame
Morbidity,rate60 days after operation
Mortality,rate60 days after operation
Length of hospital stay,days60 days after operation
Pancreatic fistula,rate60 days after operation
Bile leakage,rate60 days after operation
Intra-abdominal abscess,rate60 days after operation
wound infection,rate60 days after operation
Hemorrhage,rate60 days after operation

Other

MeasureTime frame
nonsurgical complications,rate60 days after operation

Countries

China

Contacts

Primary ContactMingqiang Lin, Dr
80218353@qq.com8605922139708
Backup ContactYanming Zhou, Dr
zhouymsxy@sina.cn8605922139708

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026