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OpenTrials
Completed

NCT Number: NCT01867567

Early Bandage Removal Post-Cesarean Delivery

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.

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Key information

Age range

18 year–44 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Ziv Medical center

Safed, 13100, Israel

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • age of 18 to 44
  • elective cesarean section, primary or repeat
  • low risk pregnancy

Exclusion criteria

  • under the age of 18 and above the age of 44
  • diabetes, preeclampsia or other pregnancy complications
  • unable or unwilling to give informed consent
  • chorioamnionitis
  • BMI over 35
  • more than 3 cesareans

Treatment and study plan

abdominal bandage

Procedure

Primary outcomes

  1. Wound Disruption

    Time frame: 5 - 7 days

Secondary outcomes

  1. Wound Infection

    Time frame: 5 - 7 days

  2. Patient satisfaction

    Time frame: 5 - 7 days

Sponsors and collaborators

Lead sponsor

Ziv Hospital

Other Gov

Registry information

Important dates

Study start
2013
Primary completion
2015
Study completion
2015
First posted
Jun 4, 2013
Registry last updated
Dec 30, 2015

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.

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