Ziv Medical center
Safed, 13100, Israel
NCT Number: NCT01867567
Women undergoing their first second or third cesarean section will be randomized into two groups. One group will have the abdominal bandage removed at 6 hours post-surgery and the other group will have the bandage removed at 24 hours. Staple removal will be at 5 - 7 days for both groups. The incision will be inspected at the time of staple removal. The 2 groups will be compared for incision disruption and infection. Also, the women will be asked about their satisfaction for time of bandage removal.
Looking for future studies?
Notify Me18 year–44 year
Female
Interventional
Not applicable
Safed, 13100, Israel
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 5 - 7 days
Time frame: 5 - 7 days
Time frame: 5 - 7 days
Ziv Hospital
Other Gov
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT02992951
Bacterial Infections, Bacterial Infections and Mycoses
Hull, East Riding of Yorkshire, United Kingdom
View Trial DetailsNCT05684198
Digestive System Diseases, Infections
Gdansk, Pomeranian Voivodeship, Poland
View Trial DetailsNCT03887299
Behavior, Cesarean Section Complications
Galveston, Texas, United States
View Trial DetailsNCT02018094
Amputation Wound, Infections
Hull, United Kingdom
View Trial Details