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Clinical Trials in Canada / NCT06701929
Recruiting Observational

The Impact of Fasting Duration on Quality of Recovery After Cesarean Section

NCT06701929 · tracked via the Priya Life Science Canada tracker
Phase
Observational
Started
2025-03-18
Last updated
2026-08-10

Condition(s) studied

Quality ImprovementQuality of Recovery From AnaesthesiaCesarean SectionFasting ( 6H for Solid ; 2H for Clear Fluid )

Study summary

This study will evaluate the effect of fasting duration and elective c-section start time on the overall quality of recovery. Patients will be seen 24 hours after surgery to answer 11 questions on their overall recovery after surgery. Several factors will be tracked to determine their effect on recovery, with the primary variable of interesting

Eligibility

Sex
FEMALE
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Presenting for elective c-section under spinal anesthesia Exclusion Criteria: * Unable to communicate in French or English * Urgent c-section * Planned general anesthesia

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Jewish General Hospital Montreal Quebec Recruiting

More Jewish General Hospital trials in Canada

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06701929 on ClinicalTrials.gov ↗ ← All trials in Canada