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Ciprofol for video-assisted thoracic surgery effect of postoperative pain in patients

Ciprofol for video-assisted thoracic surgery effect of postoperative pain in patients

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086944
Enrollment
Unknown
Registered
2024-07-15
Start date
2023-07-01
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

postoperative pain of VATS

Interventions

Ciprofol group:Anesthetic drugs use Ciprofol for induction and maintenance
Propofol group:Anesthetic drugs use Propofol for induction and maintenance

Sponsors

The First Affiliated Hospital of USTC
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Patients undergoing VATS lung surgery under elective general anesthesia (2) ASA scale 1-3 (3) Age is 18~65 years old (4) Patient compliance was good

Exclusion criteria

Exclusion criteria: (1) A history of psychiatric and neurological diseases (such as cerebrovascular disease, epilepsy, Alzheimer's disease, schizophrenia and depression, etc.) (2) Patients with multiple chronic diseases who cannot tolerate surgical anesthesia (3) Severe heart, pulmonary and renal dysfunction (4) Abnormal blood coagulation function (5) Recent history of propofol or cypofol drug use (6) Patients with related drug allergy history and contraindications (7) Patients with a history of chronic chest pain

Design outcomes

Primary

MeasureTime frame
Mechanical pain threshold;VAS scale;

Secondary

MeasureTime frame
Opioid dosage;Intraoperative hemodynamic-related measures;Incidence of nausea and vomiting;

Countries

China

Contacts

Public ContactYanhu Xie

The First Affiliated Hospital of USTC

xyh200701@sina.cn+86 139 5601 3081

Outcome results

None listed

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