Evaluation the Impact of Subcutaneous Irrigation on Wound Complications

Cesarean Section; Complications, Wound, Hematoma Clinical Trial

Official title:

Evaluation the Impact of Subcutaneous Irrigation on Wound Complications

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03321175
• Other study ID #: 2017/219
• Status: Completed
• Phase: N/A
• First received: October 22, 2017
• Last updated: April 3, 2018
• Start date: October 23, 2017
• Est. completion date: March 30, 2018

Study information

• Verified date: April 2018
• Source: Kanuni Sultan Suleyman Training and Research Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

to evaluate the effect of subcutaneous irrigation on wound complications

Description:

Cesarean section is the most common abdominal operation performed worldwide. As with every other surgical procedure, it is sometimes accompanied by surgical complications. Wound complications are encountered in approximately 5% of women that undergo CS and include haematomas, seromas and infection. To evaluate the effects and benefits of subcutaneous irrigation during cesarean section we decide to conduct this randomized study.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 185
• Est. completion date: March 30, 2018
• Est. primary completion date: March 30, 2018
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 40 Years

Eligibility

Inclusion Criteria:

• Age 18-40, undergoing cesarean section

Exclusion Criteria:

• patients with systemical disease, body mass index>30

Related Conditions & MeSH terms

• Cesarean Section; Complications, Wound, Hematoma
• Hematoma
• Wounds and Injuries

Intervention

Other:
• subcutaneous saline irrigation
200 cc saline irrigation

Locations

Country	Name	City	State
Turkey	Kanuni SSTRH	Istanbul

Sponsors (1)

Lead Sponsor	Collaborator
Kanuni Sultan Suleyman Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	wound complications	wound complications will be evaluated 1 week after the surgery.	1 week