Skip to content

TOF andPTC monitoring in thoracic surgery

TOF andPTC monitoring in thoracic surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-15007117
Enrollment
Unknown
Registered
2015-09-20
Start date
2015-08-20
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

No target disease

Interventions

Two groups: TOF monitoring andPTC monitoring:Maintaining TOF count 1 to 2 in TOF group andPTC 1 to 5 in PTC group

Sponsors

Shanghai chest hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: After written informed consent,general thoracic patients with physical status classed as I to II according to the American Society of Anesthesiologists ASA-classification aged 18–65 years were enrolledthere body mass index (BMI) are between 18 and25 kg/m2.

Exclusion criteria

Exclusion criteria: Patients were excluded if they have significant renal or hepatic dysfunction, a known neuromuscular disease anda known allergy to one of the drugs used in this study

Design outcomes

Primary

MeasureTime frame
The incidence of intraoperative adverse events;

Countries

China

Contacts

Public ContactXu Meiying
xumeiyingxk@163.com+86 18930857162

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 22, 2026