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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
AgeNot listed
SponsorJewish General Hospital

About this trial

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 criteria

This trial does not accept healthy volunteers

Qualifiers

Presenting for elective c-section under spinal anesthesia

Disqualifiers

Unable to communicate in French or English

Urgent c-section

Planned general anesthesia

Trial population

All patients presenting to the Jewish General Hospital for elective cesarean section under spinal anesthesia will be considered for inclusion.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Obstetric Quality of Recovery (ObsQoR-11)

Obstetric quality of recovery after c-section, which has been validated based on the total score of 11 questions, with total scores ranging from 0 to 110, where 0 is the worst, and 110 is the best.

Time frame
3 months

Secondary outcomes

1

Nausea & Vomitting

The presence of nausea vomiting or retching during or within 24 hours of surgery

Time frame
24 hours
2

Numeric Rating Scale (NRS) Pain Score 2 hours after surgery

Rating of pain, on a scale where 0 is no pain, and 10 is the worst pain imaginable.

Time frame
2 hours after surgery

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.