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Effect of intraoperative low-pressure ventilation intervention on intraoperative blood loss in ovarian tumour surgery: a randomised controlled trial.

Effect of intraoperative low-pressure ventilation intervention on intraoperative blood loss in ovarian tumour surgery: a randomised controlled trial. - Effect of intraoperative low-pressure ventilation intervention on intraoperative blood loss in ovarian tumour surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000053995
Enrollment
80
Registered
2024-04-01
Start date
2024-04-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ovary cancer

Interventions

Low-pressure ventilation and low venous pressure interventions are continued from the start of surgery until the end of surgery. The intervention group is managed with zero PEEP and TV 6 ml/kg, and p

Sponsors

Chiba University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Patients undergoing ovarian cancer surgery at Chiba University Hospital.

Exclusion criteria

Exclusion criteria: 1.Minors 2.Emergency surgery 3.Patients for whom an experimental laparotomy will be performed in this surgery 4.Obese with a BMI of 30 or more 5.Patients diagnosed with chronic obstructive pulmonary disease 6. Patients under treatment for asthma (included in eligible patients if only pre-existing) 7.Patients with complications of heart failure 8.Patients with severe sleep apnoea syndrome 9.Smokers (if they have not stopped smoking for at least one month) 10.Anaemia Hb <9g/dl 11.Coagulation abnormalities APTT > 42 seconds, PT > 17 seconds 12.Platelets <100,000 13.Patients with preoperative physical status 4 or 5 of the American Society of Anaesthesiologists 14.Patients with a history of laparotomy (excluding exploratory laparotomy due to ovarian cancer) 15.Patients with ChildB or C cirrhosis 16.Patients deemed unsuitable as subjects by the principal (sub)investigator

Design outcomes

Primary

MeasureTime frame
intraoperative blood loss

Secondary

MeasureTime frame
Estimated blood loss Perioperative transfusion volume and transfusion rate Estimated and actual ascites volume Postoperative chest x-ray for atelectasis Estimated blood loss at 1 week post-operatively Respiratory events at 1 week postoperatively Postoperative complications Clavien-Dindo classification at 1 week and 30 days Length of hospital stay In-hospital mortality

Countries

Japan

Contacts

Public ContactKyongsuk Son

Chiba-University Hospital Department of Anesthesiology

adya5599@chiba-u.jp0432227171

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026