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To explore the difference between sevoflurane and propofol in modified oxygenation index of patients undergoing gynecological laparoscopic surgery: a randomized controlled study

To explore the difference between sevoflurane and propofol in modified oxygenation index of patients undergoing gynecological laparoscopic surgery: a randomized controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200065644
Enrollment
Unknown
Registered
2022-11-10
Start date
2022-11-30
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

gynecological disease

Interventions

First:Propofol
Second:Sevoflurane

Sponsors

The University of Hong Kong-Shenzhen Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 45 Years

Inclusion criteria

Inclusion criteria: Female, ASA ?-?, BMI <= 30, age 20-45 years, intended to undergo gynecological laparoscopic surgery.

Exclusion criteria

Exclusion criteria: Patients with preoperative hypertension, diabetes, cardiopulmonary insufficiency, liver and kidney dysfunction, long-term smoking, and patients with neurological diseases who could not understand and cooperate with the test were excluded.

Design outcomes

Secondary

MeasureTime frame
respiratory parameter;—

Primary

MeasureTime frame
Blood Gas Analysis;—

Countries

China

Contacts

Public ContactJiang Tao

The University of Hong Kong-Shenzhen Hospital

jiangt@hku-szh.org+86 13510908346

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026