Labor and Delivery Clinical Trial
Official title:
Does Oral Intake During Labor and Delivery Have an Effect on Complications and Outcome
The recommendations regarding eating and drinking during the labor and delivery process are
not clear.
The objective of this study is to assess whether eating and drinking during the labor process
improves obstetric outcomes and maternal satisfaction.
Patients admitted for the birthing center during the first stage of the delivery and after
having a regional anesthesia are instructed as a routine in our birthing center for fasting
and drinking only water and clear fluids during their stay at the labor and delivery room and
until after giving birth.
The patients will be asked if they are interested in participating in the study. A patient
that is interested will be randomized to join one of the two arms: Fasting arm, with the
routine management of water and clear fluids or eating, she will be asked to eat every 2
hours or less a food from a list supplied by the study team.
The list of food was created with the anesthesiologist team according the review board
demand.
The data regarding the patients' history, pregnancy and labor and delivery process.
Obstetrical and neonatal outcome will be collected. A satisfactory questioner well be sent to
all participants.
Status | Recruiting |
Enrollment | 500 |
Est. completion date | February 1, 2021 |
Est. primary completion date | December 1, 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 45 Years |
Eligibility |
Inclusion Criteria: - Pregnancy at 37 weeks or more - After an epidural anaesthesia Exclusion Criteria: - Preterm delivery before 37 weeks of pregnancy - Known anomalies or chromosomal abnormalities - Patient at increased risk for aspiration based on anesthesiologist assesment - A patient post epidural anesthesia with pain indicating the need for a new epidural insertion |
Country | Name | City | State |
---|---|---|---|
Israel | Meor Medical hospital | Kfar Saba |
Lead Sponsor | Collaborator |
---|---|
Meir Medical Center |
Israel,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | prolonged second stage of labor | The mean time from full dilatation to the delivery of the baby on each group | the delivery | |
Primary | duration of pushing | The mean time from beginning of pushing with the midwife to the delivery of the baby in each group | the delivery | |
Primary | operative vaginal delivery | The mean incidence of operative vaginal delivery in each group | the delivery | |
Primary | cesarean section | The mean incidence of cesarean section in each group | the delivery | |
Secondary | Maternal satisfaction | The median satisfaction from the delivery of the mother of the delivery process from 1-11 | from 2 days after delivery until 6 months after the delivery , she will be asked once |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT04102644 -
Limiting Adverse Birth Outcomes in Resource-Limited Settings
|
||
Completed |
NCT01990612 -
A Randomized Trial of Induction Versus Expectant Management
|
N/A | |
Completed |
NCT03364491 -
Tranexamic Acid for the Prevention of Obstetrical Hemorrhage After Cesarean
|
Phase 3 | |
Withdrawn |
NCT02803450 -
Epidural Loading: High Volume, Low Concentration
|
N/A |