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Effect of Different Inspired Oxygen Fractions on Postoperative Nausea and Vomiting in Patients Undergoing Orthopedic Surgery Under General Anesthesia

Effect of Different Inspired Oxygen Fractions on Postoperative Nausea and Vomiting in Patients Undergoing Orthopedic Surgery Under General Anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600121370
Enrollment
Unknown
Registered
2026-03-30
Start date
2026-03-30
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Postoperative Nausea and Vomiting

Interventions

Control group:30% Inspired Oxygen Fractions during operation
Experimental group:80% Inspired Oxygen Fractions during operation

Sponsors

Huashan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Age: 18–65 years (2) ASA physical status: I–II (3) Patients scheduled for elective orthopedic surgery under general anesthesia, including: (4) Spine surgery: involving procedures of the cervical, thoracic, and lumbar spine, etc. (5) Joint surgery: including open or arthroscopic procedures of the ankle, knee, hip, shoulder, elbow, etc.

Exclusion criteria

Exclusion criteria: (1) Severe cardiopulmonary or cerebral diseases: chronic obstructive pulmonary disease (COPD, GOLD stage = 3); pulmonary hypertension (mPAP = 25 mmHg); uncontrolled heart failure (NYHA class = III); history of myocardial infarction or cerebral infarction. (2) Special populations: pregnant or lactating women; patients undergoing emergency surgery; patients who received antiemetic medications (e.g., tropisetron, dexamethasone) or steroids within 24 hours preoperatively; patients requiring beach chair or sitting positions during surgery. (3) Other confounding factors: history of drug or alcohol dependence; severe psychiatric disorders or communication barriers; known allergy to any anesthetic agents used in the study protocol.

Design outcomes

Primary

MeasureTime frame
the incidence of postoperative nausea and vomiting within 24 hours after surgery;

Secondary

MeasureTime frame
Severity of postoperative nausea;Incidence of postoperative severe vomiting;Incidence of postoperative adverse events;

Countries

China

Contacts

Public ContactQiong Yu

Huashan Hospital, Fudan University

yu_qiong816@sina.com+86 21 5288 9999

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026