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Phase 4 N=60 Randomized Double-blind Prevention

Role of Propofol Postconditioning on Oxidative Stress and Cognitive Function

Cerebral Arterial Aneurysm

Enrolled (actual)
60
Serious AEs
0.0%
Results posted
Sep 2016
Primary outcome: Primary: Evidences of Clinically Definite Oxidative Stress Confirmed by ELISA Kit — 72.87; 74.02; 67.10; 65.91 U/ml

Study Design & Population

Study type
Interventional
Phase
Phase 4
Interventions
propofol postconditioning (Drug); sevoflurane (Drug)
Age
Pediatric, Adult, Older Adult
Sex
All
Sponsor
The Third Central Clinical College of Tianjin Medical University
Primary completion
Dec 2015

Outcome Measures

OutcomeResultp-value
PRIMARY
Evidences of Clinically Definite Oxidative Stress Confirmed by ELISA Kit
72.87; 74.02; 67.10; 65.91; 66.74; 51.58
PRIMARY
Evidences of Clinically Definite Oxidative Stress Confirmed by ELISA
1.15; 1.18; 1.19; 1.22; 1.54; 1.70
PRIMARY
Evidences of Clinically Definite Oxidative Stress:Micronuclei
185.83; 186.40; 194.57; 195.73; 230.77; 375.87
PRIMARY
Evidences of Clinically Definite Oxidative Stress Confirmed by High Performance Liquid Chromatography
12.67; 12.22; 6.13; 6.12; 6.71; 5.91
PRIMARY
Evidences of Clinically Definite Oxidative Stress: Nuclear Buds
50.40; 53.93; 54.33; 57.43; 61.10; 62.87
PRIMARY
Evidences of Clinically Definite Oxidative Stress: Nucleoplasmic Bridges
66.50; 68.73; 78.77; 80.80; 88.40; 96.23
SECONDARY
Mini Mental State Examination (MMSE)
27.63; 27.23; 23.40; 17.73; 24.43; 20.33
SECONDARY
Montreal Cognitive Assessment (MoCA)
20.43; 19.87; 21.53; 19.20; 22.53; 20.80

Summary

The purpose of this study was to evaluate differences between propofol postconditioning and sevoflurane anesthesia in the intracranial aneurysm surgery about antioxidant effect.

Eligibility Criteria

Inclusion Criteria

  • Clinical diagnosis intracranial aneurysm surgery ,
  • American Society of Anesthesiologists (ASA)Ⅰ-Ⅱ.

Exclusion Criteria

  • severe hepatic and renal dysfunction
  • coagulation disorder
  • taking antioxidant perioperative period
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02691416). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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