Viewing Study NCT06547177



Ignite Creation Date: 2024-10-26 @ 3:37 PM
Last Modification Date: 2024-10-26 @ 3:37 PM
Study NCT ID: NCT06547177
Status: COMPLETED
Last Update Posted: None
First Post: 2022-12-20

Brief Title: The Effect of Nutrition and Fluid Intake in the First Stage of Labor
Sponsor: None
Organization: None

Study Overview

Official Title: The Effect of Nutrition and Fluid Intake in the First Stage of Labor on Maternal and Fetal Outcomes
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: Birth is a process that requires large amounts of energy As a result of skeletal and smooth muscle contractions at birth the bodys basal metabolic rate energy requirement hydration requirement and insensible fluid loss are significantly increased Information regarding the safety and effectiveness of increased hydration during labor is still controversial There is no consensus on whether this hydration should be given with intravenous solutions or orally The study aims to determine the effect of fluid intake in labor on the delivery process maternal-fetal outcomes and postpartum satisfaction of the mother
Detailed Description: Method of Study The study was planned as a randomized controlled experimental study to evaluate the effect of fluid intake during labor on mothers and babies

Location and Characteristics of the Research The research will be conducted in the delivery room of Sakarya Training and Research Hospital

Population and Sample of the Study The research will consist of pregnant women who apply to Sakarya Training and Research Hospital with signs of the onset of labor and will have an expected vaginal delivery in the delivery room Annually 7000-8000 women give birth in the hospital and approximately 50 have an expected vaginal delivery All pregnant women who met the sampling criteria and volunteered to participate in the study during the studys implementation will be included The research will be carried out in 3 groups experimental and control groups The study will be conducted with a total of 90 pregnant women 30 of whom are in each group

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