Effects of Prone Position After Major Abdominal Surgery

Last updated: May 29, 2024
Sponsor: Vastra Gotaland Region
Overall Status: Active - Recruiting

Phase

N/A

Condition

Surgery

Bronchitis (Pediatric)

Treatment

prone position

Clinical Study ID

NCT05630443
2021-06877-01
  • All Genders

Study Summary

Evaluation of postoperative prone position after major abdominal surgery. A randomized clinical trial of 100+100 patients and further add a voice/speech/singing protocol.

Eligibility Criteria

Inclusion

Patients eligable for abdominal surgery aim to cure with:

Inclusion Criteria:

  • malignancy of the esophagus, gastric- or pancreas

Exclusion

Exclusion Criteria:

-.not able to understand Swedish in writing or speaking

  • preoperatively unable to perform a prone position

Study Design

Total Participants: 200
Treatment Group(s): 1
Primary Treatment: prone position
Phase:
Study Start date:
October 01, 2022
Estimated Completion Date:
December 31, 2026

Study Description

Evaluation of postoperative prone position after major abdominal surgery. A randomized clinical trial of 100+100 patients and further add a voice/speech/singing protocol.

The patients will be randomized to the standard ERAS-protocol, enhanced recovery after surgery with or without adding periods of prone position after surgery.

They will be followed by protocol both as a momentum effect (experimental study) on POD 2-5 and also POD 7.

The aim is evaluation of prone position in order to improve the ventilation and hopefully diminish the risk of for example pneumonia and thromboembolism.

Inclusion criteria Patients referred to the Department of Surgery for major abdominal surgery of the esophagus, gastric- or pancreas surgery aim to cure.

Exclusion criteria Patients unable to understand Swedish in writing or speaking, preoperatively unable to perform a prone position.

The participation is voluntary and demands an inform consent from the patient operated upon.

The primary outcome is oxygen saturation and lung complications after surgery.

The secondary outcome is measurement of lung volumes, patient experience (7th graded Lickert scale), days of hospital care, 30 days complications etc.

Further investigations are perioperative properties as BMI, other forms of surgery, etc., and continues measurement of blood pressure, respiration frequency, heartrate, tubes and drainages, postoperative analgesic, blood samples with signs of bleeding, inflammation, infection.

Connect with a study center

  • Dept of Surgery

    Göteborg,
    Sweden

    Active - Recruiting

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