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Postoperative Comput Tomography as a Predictor of Postoperative Complications After Pancreatic Surgery

C

CHU de Reims

Status

Completed

Conditions

Pancreatectomy

Treatments

Procedure: CT scan

Study type

Interventional

Funder types

Other

Identifiers

NCT02814812
PO14086

Details and patient eligibility

About

Pancreatectomy represents the classic approach for resectable lesions of the pancreas, duodenum and periampullary region. Due to the technical skills required, the complex anatomy and the extreme fragility of the pancreatic parenchyma, pancreatic resection is still considered to be at risk of postoperative complication mainly due to pancreatic juice leaks. Anastomotic leaks are the major cause of morbidity and in-hospital mortality due to the activation of pancreatic enzymes and the following infectious and hemorrhagic complications. Severe complications negatively affect postoperative outcomes, long-term survival, quality of life, and costs. Operative mortality traditionally has been defined as the rate within 30 days or during the initial hospitalization. But in pancreatic surgery mortality rates within 90 days after pancreatic resection are double those at 30 days. In the present study, the investigators sought to evaluate the usefulness of postoperative CT-scan on the seventh postoperative day before discharging the patients to detect undiagnosed postoperative complication.

Enrollment

80 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Will be included in this study, patients:

  • Having an indication of pancreatic surgery
  • In scheduled surgery
  • Agreeing to participate in the research (ie who signed the informed consent to research participation)
  • >18yo

Exclusion criteria

Will not be included in this study, patients:

  • With emergency surgery
  • Protected by law
  • Under 18 years
  • Presenting an against-indications to the scanner: documented severe allergy to contrast material, kidney failure against-showing the contrast medium injection, pregnancy, lactation and/or MRI (pacemaker, metallic intraocular foreign body)

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

80 participants in 1 patient group

pancreatic surgery
Experimental group
Treatment:
Procedure: CT scan

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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