TCTR20240321004CompletedNot Applicable
Optimal End-Tidal Sevoflurane concentration in patients with shock undergoing general anesthesia
KhonKaen university0 sites15 target enrollmentStarted: March 21, 2024Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 15
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Observational
Eligibility Criteria
- Ages
- 18 Years to 65 Years (—)
- Sex
- All
Inclusion Criteria
- •1. Aged 18 to 65 years old
- •2. Patients with shock undergoing general anesthesia
Exclusion Criteria
- •1. Decline to participate in the study
- •2. Pregnancy
- •3. History of seizures
- •4. History of Malignant hyperthermia
- •5. History of regular alcohol consumption
- •6. Patients with neurological conditions
- •7. End-stage kidney or liver disease
- •8. Who are unable to apply bispectral index monitor
Investigators
Similar Trials
Not yet recruiting
Phase 3
Minimum dose of anaesthetic agent required for securing intravenous cannula in children undergoing eye surgeryCTRI/2017/08/009456Department of Anaesthesia
Completed
Phase 3
Requirement sevoflurane (an anesthetic agent) for two airway devices placementCTRI/2014/04/004517Post Graduate Institute of Medical Education and Research
Not yet recruiting
Not Applicable
Adequate concentration of Anaesthetic agent for the safe removal of two supra-glottic airway devices in anesthetized adults.CTRI/2018/05/013968Medical College Baroda Vadodara
Completed
Phase 3
Sevoflurane and desflurane concentration for the removal of the ProSeal Laryngeal Mask AirwayCTRI/2012/12/003250Post Graduate Institute of Medical Education and Research40
Not yet recruiting
Phase 1
comparing the level of sevoflurane needed for adequate general anaesthesia using 2 different drugs-lignocaine vs morphineCTRI/2023/11/060084AMRITA INSTITUTE OF MEDICAL SCIENCES
