Could a simple stitch prevent a common complication after pancreatic surgery?
NCT ID NCT07681128
First seen Jul 02, 2026 · Last updated Jul 02, 2026
Summary
This trial investigates whether adding a Braun anastomosis—a connection between two loops of the small intestine—during pancreatic cancer surgery can lower the risk of delayed gastric emptying, a frequent complication where the stomach takes too long to empty. About 264 adults scheduled for pancreaticoduodenectomy will be randomly assigned to receive either the standard reconstruction or the standard plus Braun anastomosis. The study aims to provide clear evidence on whether this extra step improves recovery and reduces hospital stays.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Braun anastomosis (a surgical procedure)
- What this could lead to
- If effective, this simple surgical addition could reduce delayed gastric emptying, shorten hospital stays, and improve recovery after pancreatic cancer surgery.
- What could go wrong
- Previous studies have shown mixed results, and the extra surgical step may increase operation time or technical difficulty without clear benefit.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 264 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2026
- Expected to finish
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Sep 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age ≥ 18 years, male or female; * Scheduled to undergo curative pancreaticoduodenectomy (PD); * Undergoing PD for malignant or borderline tumors, with planned antecolic Billroth II reconstruction; * Mentally competent and able to provide written informed consent. Exclusion Criteria: * Age \< 18 years; * Prior diagnosis of gastroparesis; * Benign disease as the indication for PD; * Previous history of upper gastrointestinal surgery; * Preoperative pyloric obstruction; * Planned pylorus-preserving pancreaticoduodenectomy (PPPD); * Patients who have received neoadjuvant or conversion therapy; * Preoperative glycated hemoglobin (HbA1c) \> 7.5%; * Preoperative total bilirubin level \> 200 μmol/L; * Unable or unwilling to provide written informed consent.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Tianjin Medical University Cancer Institute & Hospital
RECRUITINGTianjin, Tianjin Municipality, 300060, China
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