Effect of Ciprofol on Intraoperative Hypotension in Elderly Patients Receiving Renin-angiotensin System Inhibitors

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age65+
SponsorSecond Affiliated Hospital, School of Medicine, Zhejiang University

About this trial

The prevention of intraoperative hypotension could reduce postoperative organ injury and mortality, particularly in elderly patients receiving long-term renin-angiotensin system inhibitors. Previous meta-analyses suggest that ciprofol, a novel intravenous anesthetic agent, may provide improved hemodynamic stability compared to propofol; however, its precise effects on perioperative hemodynamics remain unclear. The study will assess whether ciprofol improves perioperative hemodynamic stability in elderly patients receiving renin-angiotensin system inhibitors.

Eligibility criteria

Qualifiers

Patients undergoing elective abdominal surgery under general anesthesia

Duration of surgery exceeding 2 hours

Patients receiving long-term renin-angiotensin system inhibitor therapy (>3 months prior to surgery)

Age ≥ 65 years

Disqualifiers

History of allergy to opioids, propofol, or ciprofol components.

Anticipated difficult airway (limited mouth opening, restricted neck movement, or modified Mallampati grade III-IV) or difficult mask ventilation.

Severe hepatic dysfunction (total bilirubin ≥3.0 mg/dL or AST/ALT ≥2 times the upper limit of normal).

Severe renal impairment (creatinine clearance ≤30 mL/min).

Trial design

Treatments tested in this trial

  • Ciprofol group
  • Propofol group

Treatment groups

140 Participants
are divided into 2 treatment groups