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Efficacy of the Transversus Abdominis Plane Block on Analgesia After Cephalic Duodeno-pancreatectomy (TAP-Block)

U

University Hospital, Strasbourg, France

Status

Completed

Conditions

Pancreatic Neoplasms

Study type

Observational

Funder types

Other

Identifiers

NCT05546970
8703 (Other Identifier)

Details and patient eligibility

About

Pancreatic duodenectomy is one of the treatments offered to patients with neoplastic disease of the pancreas. In France, in 2018, 14,000 duodeno-pancreatectomies were performed, including 140 at the Hautepierre hospital at the Strasbourg University Hospital. Pancreaticoduodenectomy is a major surgery, causing significant postoperative pain that should be minimized through multimodal analgesia involving in particular locoregional anesthesia. Since 2019, the recommendations of the ERAS company concerning ERAS (Improved Rehabilitation After Surgery) after pancreaticoduodenectomy recommend the establishment of thoracic epidural analgesia in order to limit postoperative pain. When there is a contraindication to the placement of a thoracic epidural, in particular due to arterial and/or venous vascular reconstructions requiring potential perioperative curative anticoagulation, the administration of local anesthetic by pericatricial catheter is recommended. recommended. The Transversus Abdominis Plane (TAP) block has proven analgesic efficacy, safety and harmlessness in colorectal surgery.

Enrollment

80 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Major subject (≥18 years of age)
  • Subject operated at HUS for cephalic duodeno-pancreatectomy between 01/01/2018 and 01/04/ 2022.
  • Subject who has not expressed an objection to the reuse of their data for scientific research purposes.

Exclusion criteria

  • Subject having expressed his/her opposition to participate in the study
  • Admission in intensive care unit after the operation
  • Morphine treatment at home
  • Drug addiction, weaned or not

Trial contacts and locations

1

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Central trial contact

Julie GAUDEFROY, MD

Data sourced from clinicaltrials.gov

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