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Comparison of the effects of ciprofol and propofol on cerebral oxygen saturation in patients undergoing thoracoscopic surgery: a randomized controlled study

Comparison of the effects of ciprofol and propofol on cerebral oxygen saturation in patients undergoing thoracoscopic surgery: a randomized controlled study

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600120365
Enrollment
Unknown
Registered
2026-03-12
Start date
2026-03-01
Completion date
Unknown
Last updated
2026-03-16

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

Conditions

Perioperative cerebral oxygen management-related disorders associated with thoracoscopic surgery

Interventions

Ciprofol Group:1. Anesthesia induction: Intravenous bolus of ciprofol 0.4mg/kg (injection >60s), simultaneous bolus of sufentanil 0.3µg/kg and cisatracurium besylate 0.15mg/kg (injection >20s). Loss o
the anesthesia maintenance protocol after thoracotomy is the same as the ciprofol group. 3. Position operation: The time and method of position conversion are the same as the ciprofol group, included

Sponsors

Affiliated Hospital of North Sichuan Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-65 years, regardless of gender; 2. Scheduled for elective thoracoscopic lobectomy/wedge resection/segmentectomy; 3. ASA physical status classification Grade I-III; 4. BMI 18.0-30.0kg/m²; 5. Preoperative bilateral rSO2 >=65% (monitored by FNGINMED EGOS-600A); 6. Normal preoperative cognitive function (MMSE score: illiterate >=17 points, primary school education >=20 points, middle school education and above >=24 points); 7. Written informed consent signed by patients and their family.

Exclusion criteria

Exclusion criteria: 1. History of cerebrovascular disease (stroke, transient ischemic attack) or severe intracranial lesions; 2. Severe cardiopulmonary dysfunction (NYHA cardiac function Grade III-IV, FVC176µmol/L, blood urea nitrogen >7.1mmol/L, Child-Pugh Grade B and above); 4. Hypersensitivity to ciprofol, propofol, sevoflurane or cisatracurium besylate; 5. Use of sedative-hypnotics, opioids or antipsychotics within 1 week before surgery; 6. Forehead skin injury that cannot attach rSO2 probe; 7. Pregnant or lactating women, or those planning to become pregnant within 3 months.

Design outcomes

Primary

MeasureTime frame
AUC of rSO2 deviation from baseline during induction to thoracotomy;

Secondary

MeasureTime frame
MMSE scores at 6h, 12h, and 24h after surgery;Incidence of postoperative cognitive dysfunction;MAP values at T0-T8 time points;HR values at T0-T8 time points;Maximum decrease of MAP during induction to thoracotomy;Incidence of hypotension during induction to thoracotomy;Time to loss of consciousness;Total dosage of ciprofol/propofol during induction to thoracotomy;Dosage of vasoactive drugs during induction to thoracotomy;Incidence of injection pain during induction;Incidence of cough during induction;

Countries

China

Contacts

Public ContactJingyan Lin

Affiliated Hospital of North Sichuan Medical College

linjingyan@nsmc.edu.cn+86 159 8377 1119

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 20, 2026