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Effect of the Duration of Preoperative Fasting on Hypotension Induced by General Anesthesia in the Elderly Person

The Influence of Duration of Fluid Abstinence on Hypotension During General Anaesthesia Induction for Traumatic Hip Surgery in the Elderly

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02891122
Acronym
JEÛNE PREOP
Enrollment
56
Registered
2016-09-07
Start date
2014-10-31
Completion date
2015-07-31
Last updated
2016-09-07

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

Conditions

Preoperative Fasting and Hypotension

Brief summary

This study aims to determine if prolonged fasting represents an independent risk factor for hypotension during induction of general anesthesia in the elderly.

Detailed description

Preoperative fasting aims to reduce the risk of adverse events (eg, inhalation), but may be responsible for dehydration whose consequence is a major hypotension. This problem of hypotension is important because it (MAP \<55 mmHg) is directly correlated to the occurrence of pejorative events on the cardiac and renal level and even more so that the duration of the hypotension is long.

Interventions

None listed

Sponsors

University Hospital, Brest
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Risk Score anesthetic ASA I-III * Patients ≥ 70 years * Suffering from a femoral neck fracture to be treated surgically: * either through prosthesis, * either by intramedullary nailing (gamma nail)

Exclusion criteria

* Risk Score anesthetic ASA IV * Patient on Angiotensin Converting Enzyme (ACE) inhibitors or ARBs (ARA2) within 10 hours before surgery * Obesity (BMI\> 35) or weight \<40kg * Need to make a rapid sequence induction * Inability to achieve the femoral block (standardization of induction) or patient refusal with respect to the technique.

Design outcomes

Primary

MeasureTime frame
Follow-up of the variation of the Mean arterial pressure8 months

Countries

France

Outcome results

None listed

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