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Type of anaesthesia and male patients scheduled for lumbar surgery quality of recovery: a randomized trial comparing propofol–remifentanil total i.v. anaesthesia with sevoflurane anaesthesia

Type of anaesthesia and male patients scheduled for lumbar surgery quality of recovery: a randomized trial comparing propofol–remifentanil total i.v. anaesthesia with sevoflurane anaesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-16007987
Enrollment
Unknown
Registered
2016-02-24
Start date
2016-03-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

lumbar disease

Interventions

TIVA group:propofol–remifentanil
Sevoflurane group:sevoflurane-remifentanil

Sponsors

Southern District of Anhui Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: 1. Male patients; 2. Aged 18-64 year old; 3. BMI 18.5~24.9 kg/m2; 4. ASA physical status I-II.

Exclusion criteria

Exclusion criteria: 1. Abnormal hepatic and renal function; 2. Central nervous system diseases; 3. Communicative disorders; 4. Patients taking steroids, opioid, sedative or antiemetic drugs.

Design outcomes

Primary

MeasureTime frame
The Quality of Recovery-40(QoR-40) score;—

Secondary

MeasureTime frame
Nausea and vomiting occurrence;Remifentanil usage;Response time;Tracheal extubation time;Duration in PACU;Duration in hospital stay;—

Countries

China

Contacts

Public ContactLi Juan
huamuzi1999@126.com+86 13956005465

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 13, 2026