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NCT02775227Active, not recruitingPhase 4

HYPAR Trial - Hydrocortisone vs. Pasireotide in Reducing Pancreatic Surgery Complications

HYPAR Trial - Hydrocortisone vs Pasireotide in Reducing Pancreatic Fistula and Other Complications After Pancreatic Resection - a Prospective, Randomized, Controlled Trial

Source: ClinicalTrials.gov · Last updated 24 Aug 2020

Brief summary (registry, in English)

Pancreatic resections carry a high risk for complications, especially pancreatic fistula. Both hydrocortisone and pasireotide have been shown to be effective in reducing complications in earlier RCTs. The aim of this study is to compare the effectiveness and safety of these two drugs in preventing complications of pancreatic surgery.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
126 (actual)
First submitted
14 May 2016
Start date
May 2016
Primary completion date
Jan 2019
Lead sponsor
Helsinki University Central Hospital
NCT number
NCT02775227

What you commit to

  • Study type: Interventional · Phase 4
  • Participants enrolled: 126
  • From May 2016 to the primary completion date, Jan 2019
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Allergy or other contraindication for hydrocortisone or pasireotide
  • Pancreatic resection cancelled (e.g. disseminated cancer)

Age

  • Age \< 18 years

Other

  • Preoperative exclusion criteria:
  • Atrophic pancreas and/or dilated pancreatic duct at the site of planned pancreatic transsection (applies only to patients undergoing pancreaticoduodenectomy)
  • Total pancreatectomy planned
  • No informed consent
  • Intraoperative exclusion criteria:
  • Hard pancreas and/or dilated pancreatic duct discovered during operation (applies only to patients undergoing pancreaticoduodenectomy)
  • Total pancreatectomy is performed

Who the study is looking for

  • Patients scheduled for pancreatic surgery (pancreaticoduodenectomy, distal pancreatectomy, enucleation, or other type of pancreatic resection)

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Helsinki University Central Hospital
Coordinator of this site? Confirm its status
HelsinkiFinlandUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.