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Effect of Fospropofol Disodium Combined with Sufentanil on Attenuating Tracheal Intubation Stress Response in Geriatric Patients During General Anesthesia

Effect of Fospropofol Disodium Combined with Sufentanil on Attenuating Tracheal Intubation Stress Response in Geriatric Patients During General Anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101005
Enrollment
Unknown
Registered
2025-04-17
Start date
2025-04-21
Completion date
Unknown
Last updated
2025-04-21

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

Conditions

Hypotension

Interventions

Case series:fospropofol disodium (modified Dixon sequential method)+ sufentanil

Sponsors

Affiliated Cancer Hospital of Guizhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1 Age: 65 to 90 years old, regardless of gender; 2 Patients scheduled for elective surgery under general anesthesia with single-lumen endotracheal intubation; 3 ASA (American Society of Anesthesiologists) physical status classification I or II; 4 18 kg/m^2 < BMI < 30 kg/m^2; 5 Fully comprehend the study protocol, voluntarily participate, and provide personally signed informed consent.

Exclusion criteria

Exclusion criteria: 1 Patients not receiving standardized antihypertensive therapy or with poorly controlled blood pressure (systolic blood pressure >= 160 mmHg or = 100 mmHg); 2 Heart rate (HR) 120 bpm; 3 Uncontrolled diabetes mellitus or coronary heart disease; 4 Severe hepatic/renal dysfunction (Child-Pugh score >7, estimated glomerular filtration rate [eGFR] <30 mL/min/1.73m^2); 5 Anticipated difficult airway; 6 History of allergic diseases or hypersensitivity to the investigational drugs; 7 Family history of malignant hyperthermia; 8 Untreated or uncontrolled hyperthyroidism; 9 Participation in other drug clinical trials within the preceding 3 months; 10 Pregnancy, lactation, or intention to conceive within 1 month postoperatively; 11 History of alcoholism or substance abuse.

Design outcomes

Primary

MeasureTime frame
Endotracheal intubation response;

Secondary

MeasureTime frame
Blood pressure;Heart rate;Saturation of Peripheral Oxygen ;The injection pain;

Countries

China

Contacts

Public ContactLin Xiaofen

Affiliated Cancer Hospital of Guizhou Medical University

392737182@qq.com+86 182 8514 9556

Outcome results

None listed

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