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Desflurane vs. Sevoflurane in Endovascular Aortic Repair

B

Begoña Quintana Villamandos

Status and phase

Completed
Phase 4

Conditions

Renal Failure

Treatments

Drug: Sevoflurane
Drug: Desflurane

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT03917186
DESEVAR

Details and patient eligibility

About

Randomized Clinical Trial following the evaluation of the impact on renal function in patients undergoing endovascular aortic aneurysm repair with two anesthetics protocols (Desflurane versus Sevoflurane) on the first 24 hours after surgery.

Full description

Randomized Clinical Trial to evaluate the impact on renal function in patients undergoing endovascular aortic aneurysm repair with two anesthetics protocols (Desflurane versus Sevoflurane) on the first 24 hours after surgery.

Secondary Endpoint: Among secondary endpoints we will evaluate clinical variables such emergence and recovery characteristics (time to extubation and time to emergence-open eyes and response to verbal command), the need for postoperative mechanical ventilation, the post-anesthesia recovery score and ICU length of stay.

Enrollment

80 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • older than 18 years undergoing elective endovascular aortic repair
  • who have signed informed consent

Exclusion criteria

  • urgent surgery
  • with known hypersensitivity to Desflurane or Sevoflurane.
  • Renal failure in hemodialysis

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

80 participants in 2 patient groups

Group sevoflurane
Active Comparator group
Description:
Administration under labelling conditions
Treatment:
Drug: Sevoflurane
Group desflurane
Experimental group
Description:
Administration under labelling conditions
Treatment:
Drug: Desflurane

Trial contacts and locations

1

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Central trial contact

Begoña Quintana, PhD

Data sourced from clinicaltrials.gov

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