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Persistent Postoperative Pain After Major Emergency Abdominal Surgery

Z

Zealand University Hospital

Status

Unknown

Conditions

Chronic Postoperative Pain

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Perioperative pain is one of the most significant complaints and problems for patients undergoing major open surgery. Pain after surgery carry an abundance of consequences such as reduced mobilization, reduced nutrition intake, reduced pulmonary capacity and increased risk of complications and length of hospitalization. The literature does not supply much information on short- or longer-term outcomes of pain treatment for emergency surgery. The investigators know that for planned surgery in general around 10-50 percentage suffer from persistent postoperative pain. It is therefore important to follow-up on the longer-term outcomes after the standardized analgesic pain treatment. Based on a predefined patient group called OMEGA (Optimizing Major EMergency Abdominal surgery) the investigators hypothesize that OMEGA patients will present a significant incidence rate of patients with persistent postoperative pain and/or continued opioid/non-opioid usage. Therefore this study is to investigate the incidence of prolonged postoperative pain and opioid/non-opioid consumption in OMEGA patients at 3 month after major emergency abdominal surgery.

Enrollment

110 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • OMEGA patients (patients who have undergone major emergency abdominal surgery including the stomach, small or large bowel, or rectum for conditions such as perforation, ischemia, abdominal abscess, bleeding or obstruction)
  • Age 18 or more
  • Surgery performed within 72 hours of an acute admission or as an acute re-operation

Exclusion criteria

  • Elective laparoscopy
  • Diagnostic laparotomy/laparoscopy where no subsequent procedure is performed
  • Non-elective hernia repair without bowel resection
  • Admission or transfer to an intensive care unit

Trial design

110 participants in 1 patient group

OMEGA
Description:
Patients who have undergone major emergency abdominal surgery including the stomach, small or large bowel, or rectum for conditions such as perforation, ischemia, abdominal abscess, bleeding or obstruction.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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