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Clinical Trials in China / NCT05526534
Recruiting Not applicable

A RCT on the Preventive Effect of HFNC on Postoperative Pulmonary Complications in Patients With Gynecologic Neoplasms

NCT05526534 · tracked via the Priya Life Science China tracker
Sponsor
Sichuan Cancer Hospital and Research Institute
Phase
Not applicable
Started
2022-11-01
Last updated
2025-05-23

Condition(s) studied

Gynecologic SurgeryHigh-flow Nasal CannulaPost-operative Pulmonary Complications

Investigational drug(s) / intervention(s)

heated humidified high flow nasal cannula oxygen therapy, HFNCNasal cannula oxygen

heated humidified high flow nasal cannula oxygen therapy, HFNC: HFNC can accurately provide 21% \~ 100% oxygen concentration through air oxygen mixer. And through the heating and humidification device to provide 37℃, relative humidity of 100% gas, the maximum flow of 70L/min.

Nasal cannula oxygen: Nasal cannula oxygen has become a routine part of postoperative treatment

Study summary

Patients at high risk of post-operative pulmonary complications (PPC) will be screened out from gynecological tumor patients undergoing surgical treatment, and randomly assigned into the HFNC group and control group, which uses conventional nasal cannula oxygen therapy. The primary outcome is the incidence of PPC, including postoperative hypoxemia, atelectasis, pneumonia, etc. Secondary outcomes are the improvement of postoperative oxygenation, antibiotic use, length of hospital stay, adverse events related to oxygen therapy, etc.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
90 Years
Healthy volunteers
No
Inclusion Criteria: * Patients with gynecologic Neoplasms, including benign gynecologic tumors and malignant gynecologic tumors, who are 18 to 90 years old and are scheduled for surgical treatment in our center shall receive plain chest CT scan within 1 week before surgery, and the estimated surgical time shall be ≥2 hours, and at least one of the following conditions shall be met: 1. Assess respiratory risk in surgical patients in Catalonia (ARRSPC) ≥45 points; 2. BMI≥30; 3. Moderate to severe asthma; 4. Moderate to severe chronic obstructive pulmonary disease (COPD); 5. Smoking history ≥20 packs/year Exclusion Criteria: 1. Patients with lung metastasis of malignant tumor or primary lung malignant tumor; 2. previous lung surgery or radiotherapy; 3. the surgery involved segmental bowel resection.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Sichuan Cancer Hospital and Research Institute Chengdu Sichuan Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05526534 on ClinicalTrials.gov ↗ ← All trials in China