Skip to content

A multicenter randomized controlled study of the effects of different general anesthesia induction methods on hemodynamics in elderly patients

A multicenter randomized controlled study of the effects of different general anesthesia induction methods on hemodynamics in elderly patients

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600117874
Enrollment
Unknown
Registered
2026-01-29
Start date
2026-02-01
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

The elderly patients are prone to hypotension and arrhythmia during anesthesia induction

Interventions

P Group:Fospropfol

Sponsors

Sanbo Brain Hospital Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >=60 years old, gender is not limited; 2.American Society of Anesthesiologists (ASA) : Level I-II; 3.Body mass index (BMI) : 18.5-28 kg/m^2; 4. Elective surgery is required under general anesthesia, and the estimated operation time is greater than 30 minutes; 5.Voluntary participation and signing of the informed consent form;

Exclusion criteria

Exclusion criteria: 1. Those who have contraindications to general anesthesia or have a history of anesthesia accidents; 2. Respiratory insufficiency, obstructive pulmonary disease, presence of a difficult airway, or determination of tracheal intubation difficulty (modified Markov score level III or IV); 3. uncontrolled diabetes or high blood pressure; 4.A history of drug use, alcoholism or drug dependence; 5. Abuse or long-term use of narcotic, sedative and analgesic drugs; 6.Those who are known or suspected to be allergic to or contraindicated by the process administration of various components or protocols of the study drug (sufentanil citrate injection, propofol medium/long chain fat milk, remifentanil hydrochloride for injection, and propofol disodium for injection); 7.People with a history of mental illness; 8. Participants in any drug clinical trial within 1 month before screening; 9. Subjects who have any other factors deemed unsuitable for participation in this study by the investigator.

Design outcomes

Primary

MeasureTime frame
Incidence of hypotension during anesthesia induction;

Secondary

MeasureTime frame
Complications during the induction period of anesthesia;Total intraoperative dose of remifentanil;Use of vasoactive drugs during surgery;Serum alkaline phosphatase levels before and after surgery;

Countries

China

Contacts

Public ContactYongxing Sun

Sanbo Brain Hospital Capital Medical University

8793705@163.com+86 10 62856757

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026