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Ciprofol Accelerates Early Postoperative Immune Reconstitution in Lung Cancer Patients by Maintaining Mitochondrial Metabolic Flexibility: A Randomized Controlled Trial

Ciprofol Accelerates Early Postoperative Immune Reconstitution in Lung Cancer Patients by Maintaining Mitochondrial Metabolic Flexibility: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128988
Enrollment
Unknown
Registered
2026-07-29
Start date
2026-08-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Non-small cell lung cancer

Interventions

Ciprofol Group:Induction: 0.4 - 0.5 mg/kg, administered slowly
Maintenance: Initial infusion rate 1.0 mg/kg/h. Adjust according to BIS value (target 40 - 60) in real time, and make adjustments every 5 minutes.
Propofol Group:Induction: 1.5 - 2 mg/kg
Maintenance: TCI mode (Marsh or Schnider), target concentration 2.5 - 4 ug/ml, the adjustment target is also BIS 40 - 60.

Sponsors

Guangdong Second Provincial General Hospital (Guangdong Provincial Emergency Hospital)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Patients scheduled to undergo video-assisted thoracoscopic radical lung cancer surgery (lobectomy or segmentectomy; 2.Age range: 18 - 75 years old. Gender: No restrictions. 3.American Society of Anesthesiologists (ASA) classification grades I to II; 4.Body Mass Index (BMI) ranging from 18.5 to 28.0 kg/m^2; 5.The preoperative pathological diagnosis predicted to be primary non-small cell lung cancer (NSCLC); 6.Voluntarily participate in this study and sign the informed consent form;

Exclusion criteria

Exclusion criteria: 1.Those who had received chemotherapy, radiotherapy or immunotherapy before the surgery; 2.Those with severe immune system disorders (such as autoimmune diseases, primary immunodeficiency diseases) or those who have been taking immunosuppressants/synthetic corticosteroids for a long time (more than 3 months); 3.Combined with severe liver and kidney dysfunction (Child-Pugh grade C or eGFR < 30 ml/min/1.73m^2); 4.For those who are allergic to fat emulsion, ketamine or propofol; 5.Pregnant or lactating women; 6.Participants who also took part in other clinical studies; 7.Other circumstances that the researchers considered unsuitable for inclusion in the study;

Design outcomes

Primary

MeasureTime frame
(SRC);

Secondary

MeasureTime frame
Postoperative recovery quality;PD-1 positive rate (exhaustion marker);Physical endurance;(OCR);CD107a positive rate (degranulation function);(ECAR);NKG2D positivity rate (activation marker);Laboratory safety indicators;Adverse events;

Countries

China

Contacts

Public ContactZhang hui

Guangdong Second Provincial General Hospital (Guangdong Provincial Emergency Hospital)

zhanghui@gd2h.org.cn+86 20 89168167

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026