Water And Saline Head-to-head In The Blinded Evaluation Study Trial
Completed · Not applicable
Conditions studied: Acute Appendicitis, Abscess
In brief
Patients who are diagnosed with acute appendicitis consented and then randomized into two arms of the trial. In one arm, patients receive irrigation of the abdomen during surgery with normal saline, or salt water. In the other arm, patients receive irrigation of the abdomen during surgery with sterile water. Sometimes patients receive no irrigation if none is determined to be needed at the time of operation by the surgeon. We then followed patients after surgery for 30 days. The hypothesis of this study was that the use of sterile water as irrigation fluid during surgery in patients who have acute appendicitis will decrease the chance of a post-operative abscess or infection.
Key facts
- Study ID
- NCT02714023
- Run by
- University of Missouri-Columbia
- People needed
- 241
- Starts
- 2012-10-10
- Expected to finish
- 2017-11-29
- Last updated by the study team
- 2018-10-15
Who can join
Age: 6 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- All patients, age 6 and older, who present for an emergent or interval appendectomy to any one of the participating surgeons, meet the inclusion criteria for the study. Assent from all minors (under age 18) was obtained.
You may not qualify if…
- Pregnant patients, patients with mental handicap, Veterans, patients under 6 years old
Where it is running
- University of Missouri — Columbia, Missouri, United States
Full record on ClinicalTrials.gov
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