Perioperative Hypothermia and Sevoflurane Consumption in Elderly Patients
1 other identifier
observational
70
0 countries
N/A
Brief Summary
This prospective observational study aims to evaluate the association between perioperative hypothermia and sevoflurane consumption in elderly patients undergoing hip arthroplasty under general anesthesia. Patients aged 65 years and older will be included. Perioperative body temperature and anesthetic consumption will be recorded, and the relationship between hypothermia and anesthetic requirements will be analyzed. The findings may help clarify whether hypothermia influences anesthetic depth monitoring and anesthetic consumption in elderly surgical patients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Mar 2026
Shorter than P25 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 8, 2026
CompletedFirst Posted
Study publicly available on registry
March 12, 2026
CompletedStudy Start
First participant enrolled
March 20, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2026
CompletedMarch 12, 2026
March 1, 2026
3 months
March 8, 2026
March 8, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Sevoflurane consumption (mL/hour)
Intraoperative period
Study Arms (2)
Hypothermia cohort
Normothermia cohort
Eligibility Criteria
Patients aged 65 years and older undergoing elective hip arthroplasty under general anesthesia.
You may qualify if:
- Age ≥ 65 years
- Elective hip arthroplasty under general anesthesia
- ASA physical status I-III
You may not qualify if:
- Preoperative Mini-Cog score ≤ 2
- Neurological or psychiatric disorders affecting cognitive function
- Endocrine or metabolic disorders affecting thermoregulation
- Excessive intraoperative blood loss
- Emergency surgery
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- MD
Study Record Dates
First Submitted
March 8, 2026
First Posted
March 12, 2026
Study Start
March 20, 2026
Primary Completion
July 1, 2026
Study Completion
July 1, 2026
Last Updated
March 12, 2026
Record last verified: 2026-03