- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03475303
Effect of Early Versus Traditional Hospital Discharge on Maternal Outcome
The Effect of Early Versus Traditional Hospital Discharge on Maternal Outcome for Women Undergoing Elective Cesarean Section
This study will investigate the effect of early hospital discharge versus traditional one on maternal outcome for women undergoing elective cesarean sections.
aim of the work is to assess rate of maternal hospital revisits after early hospital discharge at 8-12 hours following elective cesarean delivery compared to the current practice of discharge at 24-48 hours postoperatively.
Study Overview
Status
Intervention / Treatment
Detailed Description
The effect of early versus traditional hospital discharge on maternal outcome for women undergoing elective cesarean section
Randomized clinical trial
Protocol of a thesis for partial fulfillment of master degree in obstetrics and gynecology
Postgraduate Student: Hebatallah Saad Sedky Mohamed Degree: M.B.B.Ch., faculty of medicine- Alexandria university (2013)
Co-DIRECTOR: Prof. Dr. Ahmed Hamdy Nagiub Abdulrahman Academic Position: professor of Obstetrics and Gynecology Department: faculty of medicine- Ain Shams University
Co-DIRECTOR: Dr. Mohamed Esmat Abbas Shawky Academic Position: Lecturer of Obstetrics and Gynecology Department: faculty of medicine- Ain Shams University
What is already known on this subject? What does this study add? The rate of cesarean delivery is increasing, in developing countries, its rate ranges from 13 to 47% of all cases of delivery (Gibbons et al 2010). Current practice is to discharge women from hospital 24-48 hours after cesarean delivery, however in some rural areas there is a common practice of earlier discharge. The effect of earlier discharge on women health is controversial. The present study will investigate the possibility of earlier discharge to reduce the cost of hospitalization and postoperative care, increase the turnover rate of obstetric hospitals and improve maternal outcome.
Many studies were concerned by early discharge of patients as there is evidence for colorectal surgery suggests that enhanced recovery programmes can reduce hospital stays by 0.5-3.5 days compared with conventional care (Fiona Paton et al 2014).
The average hospital stay following Cesarean delivery in most hospitals is 2 to 4 days (Tan et al 2012). Hospitalization allows close monitoring of women and early discovery and management of complication. Early discharge would, therefore, be a disadvantage and may delay identification and treatment of maternal and infant morbidity (National Institute of Health 2011). In contrast, several studies concluded that early discharge after Cesarean delivery is not associated with maternal readmissions (Brown et al 2011) and is associated with more maternal satisfaction and lesser cost (Umbeli et al 2010) and will decrease burden on medical facilities, increase turnover of obstetrics, reduce the cost of postoperative care, reduce rate of hospital acquired complications and Improve maternal neonatal relationship.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Egy 818
-
Cairo, Egy 818, Egypt, 11311
- Recruiting
- AinShams Maternity Hospital
-
Contact:
- Hebatallah S Sedky, M.B.B.Ch
- Phone Number: 01145797676
- Email: heba.allah_saad@yahoo.com
-
Contact:
- Mohamed E Abbas, lecturer
- Phone Number: 01007644642
- Email: moh_3smat@yahoo.com
-
Principal Investigator:
- Heba S Sedky, M.B.B.Ch
-
-
Egy818
-
Cairo, Egy818, Egypt, 11311
- Recruiting
- AinShams Maternity Hospital
-
Contact:
- Hebatallah S Sedky, M.B.B.Ch
- Phone Number: 01145797676
- Email: heba.allah_saad@yahoo.com
-
Contact:
- Mohamed E Abbas, lecturer
- Phone Number: 01007644642
- Email: moh_3smat@yahoo.com
-
Principal Investigator:
- Heba S Sedky, M.B.B.Ch
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
Age between 20 and 35 years
- Gestational age between 37-42 weeks
- BMI less than 30 kg/m2
- Have normal uncomplicated pregnancy
- Planned lower uterine segment Cesarean section
- Planned for primigravida or previous one or two Cesarean sections
- Planned to have spinal anesthesia
- Cesarean sections without intra-operative complications
- Accepting to participate in the study
Exclusion Criteria:
• Emergency Cesarean section
- Gestational age less than 37 or more than 42 weeks
- BMI 30 kg/m2 or more.
- Multiple pregnancies
- Polyhydraminos
- Abnormal placenta
- Premature rupture of membranes
- Previous abdominal surgeries or uterine surgeries
- Not more than previous two Cesarean sections
- Anemia: Hemoglobin level less than 10 g/dl
- Cesarean section with intraoperative complications
- General anesthesia
- Fibroid uterus
- RH incompatibility ( as there maybe delay of availability of anti-d immunoglobulins)
- History of complicated pregnancy or delivery
- Medical disorders(hypertension, diabetes mellitus, cardiac, pulmonary, renal, hepatic, endocrine and autoimmune disorders).
- Women refusing participating in the study
- Women having any contraindications or refusing spinal anesthesia
Study Plan
How is the study designed?
Design Details
- Primary Purpose: DIAGNOSTIC
- Allocation: NA
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: early hospital discharge
women will be discharged early from hospital 12 hours postoperatively after elective cesarean sections.
|
early hospital discharge at 8-12 hours for women undergone elective cesarean section
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Rate of maternal hospital revisits
Time Frame: one week postoperatively
|
the aim is to reduce rate of maternal hospital revisits after discharge from the hospital which will be assessed by questionnaire
|
one week postoperatively
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Maternal and family satisfaction,
Time Frame: one week postoperatively
|
the aim is to get the maximum satisfaction which will be assessed by questionnaire
|
one week postoperatively
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Hebatallah S Sedky, M.B.B.Ch, Ain Shams University
Publications and helpful links
Study record dates
Study Major Dates
Study Start (ANTICIPATED)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- Early discharge
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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