Role of Drain in Decreasing Postoperative Complications

Role of Drain in Decreasing Postoperative Complications After Cesarean Section

postoperative complications are common after cesarean section

Study Overview

• Status: Unknown
• Conditions: Cesarean Section Complications
• Intervention / Treatment: Device: Drain insertion

Detailed Description

wound infection can occur after cesarean section

• Study Type: Interventional
• Enrollment (Anticipated): 200
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Egypt
  • Giza, Egypt
    • Algazeerah

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 42 years (Adult)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: Female

Description

Inclusion Criteria:

Women undergoing cesarean section

Exclusion Criteria:

• Women who deliver by normal vaginal delivery

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Other
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Triple

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: Drain	Device: Drain insertion; insertion of a drain
No Intervention: No drain

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
The number of women who will have complications	How many women who will have complications postoperative	within 2 weeks

Collaborators and Investigators

• Sponsor: Aljazeera Hospital

Study record dates

Study Major Dates

• Study Start (Anticipated): March 2, 2020
• Primary Completion (Anticipated): July 3, 2020
• Study Completion (Anticipated): August 10, 2020

Study Registration Dates

• First Submitted: February 26, 2020
• First Submitted That Met QC Criteria: February 26, 2020
• First Posted (Actual): February 27, 2020

Study Record Updates

• Last Update Posted (Actual): February 27, 2020
• Last Update Submitted That Met QC Criteria: February 26, 2020
• Last Verified: February 1, 2020

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Pathologic Processes; Postoperative Complications
• Other Study ID Numbers: drain

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No