Ignite Creation Date:
2024-10-25 @ 7:49 PM
Last Modification Date:
2024-10-26 @ 3:37 PM
Study NCT ID:
NCT06539117
Status:
COMPLETED
Last Update Posted:
None
First Post:
2024-04-14
Brief Title:
Early Initiation of Oral Feeding Versus Traditional Feeding Post Caesarean Section
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Early Initiation of Oral Feeding Versus Traditional Feeding Post Caesarean Section A Randomized Controlled Trial
Status:
COMPLETED
Status Verified Date:
2024-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Early initiation of oral feeding within 6-12 hours post-caesarean section has been noticed to be well tolerated by patients and helps them recover fast Our study aimed to evaluate the tolerability safety and benefits of early oral feeding post-caesarean section
Detailed Description:
BACKGROUND Early initiation of oral feeding within 6-12 hours post-caesarean section has been noticed to be well tolerated by patients and helps them recover fast However the traditional method of waiting for 24 hours to commence oral feeding post-caesarean section is still being widely practiced due to the fear of post-operative ileus Though some studies have shown this fear to be unfounded early initiation of oral feeding is not yet universally accepted
OBJECTIVES To evaluate the tolerability safety and benefits of early oral feeding post-caesarean section
STUDY DESIGN AND SETTING This was a randomized control trial equivalence carried out at Alex Ekwueme Federal University Teaching Hospital Abakaliki Nigeria
METHODS Three hundred and six eligible women randomized into groups Aearly and Btraditional feeding group were admitted into the post natal ward after elective or emergency caesarean section Women in group A were commenced on graded oral sips 6 hours post- caesarean section and subsequently soft diets from the 12th hour after oral sips were well tolerated while those in group B were commenced on the same regimen as in group A 24 hours post-caesarean section
MAIN OUTCOME MEASURE Time of return of bowel sound time of resuming normal diets duration of hospital stay and post-operative complications ANALYSIS Data obtained were analyzed using the computer software IBM SPSS version 26 Frequency tables were made and results tested for significance using the t-test for continuous variables and Chi-square test for categorical variables Relative risk RR was also determined with confidence interval set at 95 and the level of significance determined by p-value 005
OBJECTIVES To evaluate the tolerability safety and benefits of early oral feeding post-caesarean section
STUDY DESIGN AND SETTING This was a randomized control trial equivalence carried out at Alex Ekwueme Federal University Teaching Hospital Abakaliki Nigeria
METHODS Three hundred and six eligible women randomized into groups Aearly and Btraditional feeding group were admitted into the post natal ward after elective or emergency caesarean section Women in group A were commenced on graded oral sips 6 hours post- caesarean section and subsequently soft diets from the 12th hour after oral sips were well tolerated while those in group B were commenced on the same regimen as in group A 24 hours post-caesarean section
MAIN OUTCOME MEASURE Time of return of bowel sound time of resuming normal diets duration of hospital stay and post-operative complications ANALYSIS Data obtained were analyzed using the computer software IBM SPSS version 26 Frequency tables were made and results tested for significance using the t-test for continuous variables and Chi-square test for categorical variables Relative risk RR was also determined with confidence interval set at 95 and the level of significance determined by p-value 005
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None