CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 140 enrolled
Drug / intervention
Not specified
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04988893
NCT04988893N/ACompleted

Quality of Recovery Scores in Parturients With Obesity: A Prospective Observational Cohort Study

In Brief

An observational study for Quality of Recovery and Post Operative Pain. Completed, enrolled 140 participants across 1 site.

Detailed Summary

The prevalence of obesity has increased dramatically recently. Obesity is a pro-inflammatory state which leads to chronic low grade inflammation having different systemic effects. This may make obesity an independent risk factor for severe acute postoperative pain. No prospective studies have been conducted to specifically evaluate the quality of recovery after caesarean delivery for women with morbid obesity when compared to non-obese parturients. In addition, while there is biological plausibility to infer worse pain scores in parturients with obesity, the magnitude of this difference is unknown and information guiding adjustments in pain management are lacking.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesCanada
Collaborators--

Timeline

N/ACompletedFinished
20222023202420252026
First PostedAug 4, 2021
Enrollment StartAug 9, 2021
Primary CompletionMar 18, 2023
TodayJul 2, 2026
Enrollment to primary: 1.6 yearsPosted 4.9 years ago