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Single-center Prospective Study: Impact of Neoadjuvant Therapy on Ciprofol Consumption in Esophageal Cancer Surgery

Single-center Prospective Study: Impact of Neoadjuvant Therapy on Ciprofol Consumption in Esophageal Cancer Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500114144
Enrollment
Unknown
Registered
2025-12-08
Start date
2025-12-15
Completion date
Unknown
Last updated
2025-12-15

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

Conditions

Esophagectomy

Interventions

Neoadjuvant therapy group:Neoadjuvant therapy (determined as necessary by medical or surgical oncologists according to guidelines
no restrictions on the choice of neoadjuvant drugs).
No neoadjuvant therapy group:No neoadjuvant therapy (determined as unnecessary by medical or surgical oncologists according to guidelines).

Sponsors

The Cancer Hospital, Shantou University Medical College
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Preoperative diagnosis of esophageal cancer, intending to perform radical esophagectomy. 2. ASA Classification I-IV.

Exclusion criteria

Exclusion criteria: 1. Open surgery; 2. Recurrence after non-surgical treatment of esophageal cancer; 3. Presence of other malignant tumors or severe mental illness; 4. Severe cardiopulmonary insufficiency; 5. Severe liver or kidney dysfunction; 6. History of adverse reactions to sedation or general anesthesia; 7. Allergy to opioids; 8. Allergy to tecresol or propofol; 9. Allergy to rocuronium bromide; 10. Long-term use of medications known to synergistically interact with propofol or HSK3486; 11. Preoperative identification of potential difficult airway.

Design outcomes

Primary

MeasureTime frame
Average dose of ciprofol (mg/kg/h);

Secondary

MeasureTime frame
Time to achieve BIS <= 60 after drug administration;Time to loss of consciousness after propofol injection;Heart rate and blood pressure at baseline, after drug administration, immediately after intubation, and 5 min after intubation;Other secondary indicators: total consumption of propofol and propofol consumption; number of intraoperative adjustments of propofol infusion rate; incidence of postoperative nausea and vomiting; time from drug discontinuation to awakening; time from drug discontinuation to eyelid movement in response to verbal stimulation; remifentanil consumption; atracurium consumption; norepinephrine consumption; incidence of MAP decrease by 30% or below 65 mmHg after drug administration but before intubatio;

Countries

China

Contacts

Public ContactSu Zegeng

Cancer Hospital Of Shantou University Medical College

goctor@163.com+86 754 8859 9623

Outcome results

None listed

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