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Early Cognitive Function in Elderly Patients After Laser Laryngeal Surgery: Des vs Prop

Early Cognitive Function and Recovery in Elderly Patients After Laser Laryngeal Surgery: Desflurane-based vs Propofol-based Anesthesia

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03194074
Acronym
POCDLLS
Enrollment
70
Registered
2017-06-21
Start date
2017-08-15
Completion date
2019-12-31
Last updated
2018-07-27

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

Conditions

Cognition Disorders in Old Age

Keywords

Laser Laryngeal Surgery, Desflurane, Propofol

Brief summary

Postoperative cognitive impairment is one of the most common complications in elderly surgical patients. Laser laryngeal surgery is a short procedure, but characterized by high risk of disastrous airway fire. So the recommended oxygen concentration is less than 30%. For elderly patients, because of preoperatively declined cardiovascular and lung function and cognitive function, there is a potential that intraoperative low oxygen concentration may lead to drop of arterial oxygen tension, decrease of brain oxygenation, and exacerbate brain function impairment. Intravenous anesthesia and inhalation anesthesia is two commonly used technique for general anesthesia. Consequently, we carry out this study to identify whether different classes of anesthetics can affect postoperative cognitive function in old patient undergoing laser laryngeal surgery.

Detailed description

The allocation sequence is generated by computer random number generation, and the allocation is placed in sequentially numbered opaque sealed envelopes by a non-investigator. Enrolment and data collection are performed by trained research staff who are not involved in the care of the patients. The treating clinicians are not blinded to the assignment group, but all other staff involved in both the collection and collation of data, and administration of neurocognitive testing, are blinded to group allocation The primary measurement is the MMS scores. The secondary measurements are intraoperative desaturation score (multiplying Spo2 \< 90% by time (seconds)), extubation time, orientation time, and time to discharge from the post-anaesthesia care unit (PACU). A sample size of 35 was determined by using a power analysis based on the assumptions that the incidence of postoperative cognitive impairment in adult after otorhinolaryngological surgery would be as high as 50 %, b) a 70% reduction (from 50% to 15%) would be of clinical significance, and c) α= 0.05, β= 0.2. The continuous variables were expressed as means ± standard deviation (SD) whereas categorical variables were expressed as frequency and percentage for data description. The outcome of interest is cognitive decline. A Generalized estimating equation (GEE) model with compound symmetry covariance structure was constructed to compare differences between two treatments with different time points as the repeated factors. As the effect of treatments may vary across different time points, an interaction between treatments and time was included in the model. Bonferroni-corrected post hoc test was conducted to adjust the observed significant level for multiple comparisons if the null hypothesis was rejected.

Interventions

DRUGPropofol

In propofol/remifentanil group, propofol at a rate 75\ 150 µg/kg/min and remifentanil at 0.1-0.3 µg/kg/min are maintained throughout surgery.

DRUGDesflurane

In desflurane/remifentanil group, desflurane at end tidal concentration at 0.7\ 1.0 minimum alveolar concentration (MAC) and remifentanil 0.1-0.3 ug/kg/min are used.

Sponsors

Eye & ENT Hospital of Fudan University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients scheduled for laser laryngeal surgery under general anesthesia with either Propofol or desflurane based technique.

Exclusion criteria

* Patients with cardiac, pulmonary, hepatic, or renal dysfunction, epilepsy, or uncontrolled hypertension, or those taking medications that influence the central nervous system, are excluded from the study. Patients who show obvious alteration of mental status, or refuse to participate, are also excluded from the study.

Design outcomes

Primary

MeasureTime frameDescription
Change of Mini-Mental State (MMS) test scoreChange of MMS score between two time points (the day before surgery and 30min postoperativelyChange of 30-point questionnaire that is used to measure cognitive impairment before and after surgery

Secondary

MeasureTime frameDescription
Change of Mini-Mental State (MMS) test scoreChange of MMS score between two time points (the day before surgery and 1h postoperativelyChange of 30-point questionnaire that is used to measure cognitive impairment before and after surgery

Countries

China

Contacts

Primary ContactXia Shen, M.D.
zlsx@yahoo.com8613611874118
Backup ContactHui Qiao, M.D.
theyellow@163.com8615900598163

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026