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NCT03355378 Clinical Trial

Short Versus Standard Post-operative Stay After Elective Cesarean Delivery

Cesarean Section Complications Clinical Trial

Official title:
Short Versus Standard Post-operative Stay After Elective Cesarean Delivery

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT03355378
Other study ID # POSCS
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 1, 2017
Est. completion date December 2018

Study information
Verified date July 2018
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

After major open abdominal surgery, transient paralytic ileus usually follows. It has been suggested that stimulation of pain fibers, excessive sympathetic tone, and the release of inhibitory neurotransmitters from bowel wall associated with bowel manipulation and peritoneal irritation are responsible mechanisms. There have been concerns that early postoperative oral feeding would lead to vomiting with subsequent aspiration pneumonia, anastomotic leakage, and wound dehiscence.

Recruitment information / eligibility
Status Recruiting
Enrollment 200
Est. completion date December 2018
Est. primary completion date September 2018
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 35 Years
Eligibility Inclusion Criteria:

1. Women is sure of her last menstrual period or documented early pregnancy ultrasound.

2. Women aged 20-35 years.

3. Women with Body mass index18-22 kg/m2.

4. Estimated gestational age is ranging between 37-40 weeks gestation.

5. Accepting to participate in the study.

Exclusion Criteria:

1. Smoker = 11 cigarettes/day.

2. Caesarean hysterectomy .

3. Surgical management of severe postpartum haemorrhage .

4. History of bowel obstruction , inflammatory bowel disease .

5. Previous abdominal or pelvic radiation

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• gum chewing
chewing gum orally for 30 minutes

Locations
Country Name City State
Egypt Assiut Faculty of Medicine Assiut

Sponsors (1)
Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary duration of hospital stay time of postoperative recovery of gastrointestinal tract 48 hours
See also
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Not yet recruiting NCT06060327 - Comparing Tranexamic Acid Versus Ecbolics in Preventing Hemorrhage During and After Cesarean Section N/A
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