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Appropriate Compatibility of Propofol and Sevoflurane for Orthopaedic Surgery of Patients With MCI

T

The Third Central Clinical College of Tianjin Medical University

Status

Unknown

Conditions

Cognitive Impairment, Mild

Treatments

Drug: Sevoflurane
Drug: Propofol

Study type

Interventional

Funder types

Other

Identifiers

NCT03165396
szxlcyj-chen

Details and patient eligibility

About

According to the inclusion and exclusion criteria, elderly patients undergoing elective orthopedic surgery were randomly divided into four groups. The different combinations of propofol and sevoflurane were used in the four groups: 1 day before surgery, after patients become wide-awake, and 3 days, 7 days, and 3 months after surgery, the patient's cognitive function was evaluated using a professional cognitive scale and other indicators. Finally, statistical analysis.

Enrollment

100 estimated patients

Sex

All

Ages

50 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Elective orthopaedic surgery
  • American Society of Anesthesiologists physical status: II

Exclusion criteria

  • Neurological diseases that may affect cognitive function (e.g., subdural hematoma)
  • Hypothyroidism
  • Alcoholic dementia

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

100 participants in 4 patient groups

Propofol
Experimental group
Description:
administrated Target Controlled Infusion (TCI)of propofol (Cp 2.0\~2.5μg/ml )for maintaining
Treatment:
Drug: Propofol
1.2 μg/ml Propofol
Experimental group
Description:
administrated Target Controlled Infusion (TCI)of propofol (Cp 1.2 μg/ml )combined with appropriate sevoflurane for maintaining
Treatment:
Drug: Sevoflurane
Drug: Propofol
0.6 μg/ml Propofol
Experimental group
Description:
administrated Target Controlled Infusion (TCI)of propofol (Cp 0.6 μg/ml )combined with appropriate sevoflurane for maintaining
Treatment:
Drug: Sevoflurane
Drug: Propofol
Sevoflurane
Experimental group
Description:
administrated 1.3 minimum alveolar concentration(MAC ) sevoflurane for maintaining
Treatment:
Drug: Sevoflurane

Trial contacts and locations

1

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Central trial contact

Haiyun Wang; Yimeng Chen

Data sourced from clinicaltrials.gov

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