Quality of Recovery From Obstetric Anaesthesia - a Multicentre Study
Last updated on July 2021Recruitment
- 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