Recruitment

Recruitment Status
Not yet recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Anesthesia Morbidity
  • Obstetric Anesthesia Problems
  • Quality of Life
Type
Observational
Design
Observational Model: OtherTime Perspective: Prospective

Participation Requirements

Age
Between 18 years and 55 years
Gender
Only males

Description

An observational survey based study, for 3 consecutive week days, chosen by the local investigating team during a two-week period across multiple centres. Local investigators will complete the survey with each patient who has received anaesthetic intervention from an anaesthetist, 1 day, around 24hr...

An observational survey based study, for 3 consecutive week days, chosen by the local investigating team during a two-week period across multiple centres. Local investigators will complete the survey with each patient who has received anaesthetic intervention from an anaesthetist, 1 day, around 24hrs after delivery in line with their routine anaesthetic follow up. At 30 days, a telephone survey will be conducted with each patient to repeat the ObsQoR survey and ask key questions regarding functional recovery and activities of daily living post delivery. In addition for a small number of sites, elective caesarean delivery patients will have blood taken at the point of anaesthesia and 24 hours post delivery to assess the immune function and any changes which may predict poorer outcome in these women.

Tracking Information

NCT #
NCT04192045
Collaborators
Stanford University
Investigators
Study Chair: Kariem El-Boghdadly GSTT