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1000 Titel
  • Evaluation of robotic versus open partial pancreatoduodenectomy—study protocol for a randomised controlled pilot trial (EUROPA, DRKS00020407)
1000 Autor/in
  1. Klotz, Rosa |
  2. Dörr-Harim, Colette |
  3. Bruckner, Thomas |
  4. Knebel, Philipp |
  5. Diener, Markus K. |
  6. Hackert, Thilo |
  7. Mihaljevic, André L. |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-01-08
1000 Erschienen in
1000 Quellenangabe
  • 22(1):40
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s13063-020-04933-8 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7796523/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Background!#!Partial pancreatoduodenectomy (PD) is the indicated surgical procedure for a wide range of benign and malignant diseases of the pancreatic head and distal bile duct and offers the only potential cure for pancreatic head cancer. The current gold standard, open PD (OPD) performed via laparotomy, is associated with morbidity in around 40% of cases, even at specialised centres. Robotic PD (RPD) might offer a viable alternative to OPD and has been shown to be feasible. Encouraging perioperative results have been reported for RPD in a number of small, non-randomised studies. However, since those studies showed a considerable risk of bias, a thorough comparison of RPD with OPD is warranted.!##!Methods!#!The EUROPA (EvalUation of RObotic partial PAncreatoduodenectomy) trial is designed as a randomised controlled unblinded exploratory surgical trial with two parallel study groups. A total of 80 patients scheduled for elective PD will be randomised after giving written informed consent. Patients with borderline or non-resectable carcinoma of the pancreatic head as defined by the National Comprehensive Cancer Network guidelines, distant metastases or an American Society of Anaesthesiologists (ASA) score > III will be excluded. The experimental intervention, RPD, will be compared with the control intervention, OPD. An intraoperative dropout of approximately eight patients per group is expected because they may receive another type of surgical procedure than planned. Overall, 64 patients need to be analysed. The primary endpoint of the trial is overall postoperative morbidity within 90 days after index operation, measured using the Comprehensive Complication Index (CCI). The secondary endpoints include the feasibility of recruitment and assessment of clinical, oncological and safety parameters and quality of life and cost-effectiveness.!##!Discussion!#!The EUROPA trial is the first randomised controlled trial comparing RPD with OPD. Differences in postoperative morbidity will be evaluated to design a future multicentre confirmatory efficacy trial.!##!Trial registration!#!German Clinical Trial Register DRKS00020407 . Registered on 9 March 2020.
1000 Sacherschließung
lokal Pancreaticoduodenectomy/adverse effects [MeSH]
lokal Study Protocol
lokal Robotic surgical procedures
lokal Humans [MeSH]
lokal Pancreatoduodenectomy
lokal Randomized Controlled Trials as Topic [MeSH]
lokal Cost-benefit analysis
lokal Randomised controlled trial
lokal Robotic Surgical Procedures/adverse effects [MeSH]
lokal Postoperative complication
lokal Quality of Life [MeSH]
lokal Pilot Projects [MeSH]
lokal Pancreatic Neoplasms/surgery [MeSH]
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0003-4123-261X|https://frl.publisso.de/adhoc/uri/RMO2cnItSGFyaW0sIENvbGV0dGU=|https://frl.publisso.de/adhoc/uri/QnJ1Y2tuZXIsIFRob21hcw==|https://frl.publisso.de/adhoc/uri/S25lYmVsLCBQaGlsaXBw|https://frl.publisso.de/adhoc/uri/RGllbmVyLCBNYXJrdXMgSy4=|https://frl.publisso.de/adhoc/uri/SGFja2VydCwgVGhpbG8=|https://frl.publisso.de/adhoc/uri/TWloYWxqZXZpYywgQW5kcsOpIEwu
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1000 Erstellt am 2023-11-16T14:16:20.226+0100
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