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The Effect of IoC on Analgesia for Elderly Patients With Postoperative Effectiveness

The Effect of IoC on the Level of Intraoperative Analgesia for Elderly Patients With Postoperative Effectiveness

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02827682
Enrollment
100
Registered
2016-07-11
Start date
2016-07-31
Completion date
2018-05-31
Last updated
2017-01-20

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

Conditions

Colorectal Cancer

Keywords

IoC, monitor, elderly, postoperative effectiveness

Brief summary

The morbidity of colorectal cancer and the surgery number among elderly is growing. The investigators need to provide more advanced and specific monitoring technology for these patients. Index of consciousness (IoC) monitor is now widely used among endoscopy, cholecystectomy and other common clinical applications. The investigators goal is to verify whether using IoC monitor could help to improve the postoperative recovery after colorectal surgery.

Detailed description

Participants will be randomly assigned, in a 1:1 ratio, to receive IoC monitoring or BIS monitoring during the operation as the criteria for adjustment of analgesics use. The randomization sequence will be computer-generated, and randomization will be performed in blocks and will be stratified according to participating center. The number of dialysis and patient's recovery after the transplantation will be recorded. The participation of each patient is scheduled till they discharge from hospital.

Interventions

DEVICEAngel-6000D Multiparameter Anesthesia Monitor (IoC)

The Angel-6000D Multiparameter Anesthesia Monitor, Shenzhen Weihaokang Medical Technology Co., Ltd, Guangdong, China

DEVICEBIS VISTA Monitor (BIS)

BIS VISTA Monitor, Covidien, Changchun city shi jia trade co., Ltd, Changchun, China

Sponsors

First Affiliated Hospital Xi'an Jiaotong University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Investigator)

Eligibility

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

Inclusion criteria

* Patients aged over 60 years old that underwent Colorectal surgery in the First Affiliated Hospital of Xi'an Jiaotong University.

Exclusion criteria

* Having severe comorbidity history,for example,severe cardiac dysfunction * Having central nervous system disease, severe endocrine, and history of mental disorders * Alcoholic and long-term use of sedatives and opioids history * Drug allergy history.

Design outcomes

Primary

MeasureTime frameDescription
Duration time in PACU24 hourspatients able to leave PACU with the proper Aldrete score

Secondary

MeasureTime frame
Use of remifentanilduring surgery
Use of propofolduring surgery
length of hospital stay (LOS)Participants will be followed for the duration of hospital stay, an expected average of 2 weeks

Countries

China

Contacts

Primary ContactJing Xu, MD
xuj0909@163.com13772052823
Backup ContactQiang Wang, PHD
dr.wangqiang@139.com13991236768

Outcome results

None listed

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