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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03860129
Other study ID # RUB 4780-13-B
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 10, 2014
Est. completion date May 31, 2017

Study information

Verified date February 2019
Source Ruhr University of Bochum
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The MIRUS system (TIM, Andernach, Germany) as well as the AnaConDa uses a reflector to conserve volatile anaesthetics (VA). Both systems can be paired with ICU ventilators, but MIRUS features an automated control of end-tidal VA concentrations (etVA). We compare depth of 0.5 MAC inhalational long-term sedation with Isoflurane (ISO), Sevoflurane (SEVO) or Desflurane (DES).


Description:

The study was approved by the appropriate Institutional Review Board. Thirty ASA II-IV patients, undergoing elective or emergency surgery under general anaesthesia were included and randomized into three equal groups: ISO, SEVO or DES. We used MIRUS, a gas delivery system with a VA reflector, just like AnaConDa, that can be paired with common ICU ventilators. Additionally, MIRUS features the unique ability to maintain the end-tidal concentration (etVA) in target by automatically adjusting the delivery rate. Every 8 hours, the RASS was assessed by the nurse. The log of the EEG-Narcotrend Index (NI) was also included in the study.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date May 31, 2017
Est. primary completion date May 5, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Signing of the informed consent document (patient or relatives).

- Patient age 18 years or older.

- ASA I-III

Exclusion Criteria:

- ASA IV patients

- Epidural or spinal analgesia

- Allergy or known hypersensitivity to any of the study drugs

- Patients with known or suspected genetic susceptibility to malignant hyperthermia

- Previous participation in this trial

- Participation in another clinical trial within 4 weeks prior to selection.

- Pregnant women

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Isoflurane
Group A: Isoflurane (0.5 MAC)
Sevoflurane
Group B: Sevoflurane (0.5 MAC)
Desflurane
Group C: Desflurane (0.5 MAC)

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Ruhr University of Bochum

References & Publications (3)

Bellgardt M, Drees D, Vinnikov V, Procopiuc L, Meiser A, Bomberg H, Gude P, Vogelsang H, Weber TP, Herzog-Niescery J. Use of the MIRUS™ system for general anaesthesia during surgery: a comparison of isoflurane, sevoflurane and desflurane. J Clin Monit Comput. 2018 Aug;32(4):623-627. doi: 10.1007/s10877-018-0138-z. Epub 2018 Apr 9. — View Citation

Bomberg H, Glas M, Groesdonk VH, Bellgardt M, Schwarz J, Volk T, Meiser A. A novel device for target controlled administration and reflection of desflurane--the Mirus™. Anaesthesia. 2014 Nov;69(11):1241-50. doi: 10.1111/anae.12798. Epub 2014 Jul 9. — View Citation

Romagnoli S, Chelazzi C, Villa G, Zagli G, Benvenuti F, Mancinelli P, Arcangeli G, Dugheri S, Bonari A, Tofani L, Belardinelli A, De Gaudio AR. The New MIRUS System for Short-Term Sedation in Postsurgical ICU Patients. Crit Care Med. 2017 Sep;45(9):e925-e931. doi: 10.1097/CCM.0000000000002465. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary usage of volatile anesthetics at 0.5 MAC during ICU Sedation Comparison between Isofluarne, Sevoflurane and Desflurane up to one week
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