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Water And Saline Head-to-head In The Blinded Evaluation Study Trial (WASHITBEST)

Primary Purpose

Acute Appendicitis, Abscess

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Normal Saline
Sterile Water
Sponsored by
University of Missouri-Columbia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Appendicitis

Eligibility Criteria

6 Years - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • 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.

Exclusion Criteria:

  • Pregnant patients, patients with mental handicap, Veterans, patients under 6 years old

Sites / Locations

  • University of Missouri

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

No Intervention

Arm Label

Normal Saline

Sterile Water

No irrigation used

Arm Description

Patients were randomized to receive normal saline as an irrigation solution during appendectomy.

Patients were randomized to receive sterile water as an irrigation solution during appendectomy.

Patients who do not receive any irrigation at time of operation.

Outcomes

Primary Outcome Measures

Post-operative deep space organ infection as defined by the Surgical Infection Society
Infection after surgery within the peritoneal space

Secondary Outcome Measures

Temperature greater than 38.5 degree Celsius
Chart review for evidence of prolonged fever >38.5 for >2 days
Greater than 2 days to return of bowel function as evident by either flatus or bowel movement
Chart review for evidence of prolonged ileus for >2days
Length of Hospital Stay
Medical record will be reviewed for hospital length of stay following surgery

Full Information

First Posted
March 8, 2016
Last Updated
October 10, 2018
Sponsor
University of Missouri-Columbia
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1. Study Identification

Unique Protocol Identification Number
NCT02714023
Brief Title
Water And Saline Head-to-head In The Blinded Evaluation Study Trial
Acronym
WASHITBEST
Official Title
Water And Saline Head-to-head In The Blinded Evaluation Study Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2018
Overall Recruitment Status
Completed
Study Start Date
October 10, 2012 (Actual)
Primary Completion Date
September 10, 2015 (Actual)
Study Completion Date
November 29, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Missouri-Columbia

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
All patients, aged 6 and above, who present for an emergent or interval appendectomy to any one of the participating surgeons will potentially be enrolled in the study. Prior to surgery, the patient or the patient's guardian if a minor, will be informed of the study and consent (assent of minors will be obtained) will be requested. If consent is obtained, the patient's name and medical record number will then be sent to the inpatient pharmacy. They will be randomly assigned using a master list to either water or saline arm. The pharmacy will then send the correct solution to the operating room in the form of 3 one Liter bags. This will be ordered prior to going to the operating room. Next, a laparoscopic or open appendectomy will be performed according to the current standard of care. The surgeon will also be free to convert a laparoscopic procedure to an open procedure if deemed appropriate by his or her clinical judgment. The type of irrigant used during the case, however, will be blinded to the surgeon. The surgeon will use as much irrigation solution as they deem necessary based on an intra-operative decision. This will likely not have any affect on the study, as there is no standard amount of irrigation that is needed during appendectomies, and we do not wish to change the current practices of our surgeons. Additionally, the study question of if sterile water will decrease infectious rates will not be affected either. The science of this study will remain the same whether 10 mL or 3000 mL of irrigation solution is utilized. The surgeon may use more irrigation if deemed necessary to adequately wash the abdomen and remove all particulate matter and blood clots. At the end of the case, the surgeon will record the amount of irrigant used along with surgery date, duration of symptoms, surgery start and finish time, preoperative antibiotics, height and weight. The patient will be followed in the study for 30 days after surgery. There is usually a follow up office visit one to two weeks after the procedure. A chart review after the case will capture the length of stay, post-operative antibiotic, pathology report results, and complications consisting such as prolonged ileus (>2 days), bowel obstruction, prolonged fever (> 2 days), post-operative abscess, irrigation volume, and wound infection.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Appendicitis, Abscess

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
241 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Normal Saline
Arm Type
Active Comparator
Arm Description
Patients were randomized to receive normal saline as an irrigation solution during appendectomy.
Arm Title
Sterile Water
Arm Type
Active Comparator
Arm Description
Patients were randomized to receive sterile water as an irrigation solution during appendectomy.
Arm Title
No irrigation used
Arm Type
No Intervention
Arm Description
Patients who do not receive any irrigation at time of operation.
Intervention Type
Procedure
Intervention Name(s)
Normal Saline
Intervention Description
Intra-operative irrigation with normal saline
Intervention Type
Procedure
Intervention Name(s)
Sterile Water
Intervention Description
Intra-operative irrigation with sterile water
Primary Outcome Measure Information:
Title
Post-operative deep space organ infection as defined by the Surgical Infection Society
Description
Infection after surgery within the peritoneal space
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Temperature greater than 38.5 degree Celsius
Description
Chart review for evidence of prolonged fever >38.5 for >2 days
Time Frame
30 days
Title
Greater than 2 days to return of bowel function as evident by either flatus or bowel movement
Description
Chart review for evidence of prolonged ileus for >2days
Time Frame
30 days
Title
Length of Hospital Stay
Description
Medical record will be reviewed for hospital length of stay following surgery
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 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. Exclusion Criteria: Pregnant patients, patients with mental handicap, Veterans, patients under 6 years old
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Arthur Rawlings, MD
Organizational Affiliation
University of Missouri-Columbia
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Missouri
City
Columbia
State/Province
Missouri
ZIP/Postal Code
65212
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
21396311
Citation
Moore CB, Smith RS, Herbertson R, Toevs C. Does use of intraoperative irrigation with open or laparoscopic appendectomy reduce post-operative intra-abdominal abscess? Am Surg. 2011 Jan;77(1):78-80.
Results Reference
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23427791
Citation
Hughes MJ, Harrison E, Paterson-Brown S. Post-operative antibiotics after appendectomy and post-operative abscess development: a retrospective analysis. Surg Infect (Larchmt). 2013 Feb;14(1):56-61. doi: 10.1089/sur.2011.100. Epub 2013 Feb 21.
Results Reference
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8069421
Citation
Bonanni F, Reed J 3rd, Hartzell G, Trostle D, Boorse R, Gittleman M, Cole A. Laparoscopic versus conventional appendectomy. J Am Coll Surg. 1994 Sep;179(3):273-8.
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PubMed Identifier
9834347
Citation
Paik PS, Towson JA, Anthone GJ, Ortega AE, Simons AJ, Beart RW Jr. Intra-abdominal abscesses following laparoscopic and open appendectomies. J Gastrointest Surg. 1997 Mar-Apr;1(2):188-92; discussion 192-3. doi: 10.1016/s1091-255x(97)80108-4.
Results Reference
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PubMed Identifier
11296116
Citation
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PubMed Identifier
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Citation
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PubMed Identifier
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Citation
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PubMed Identifier
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Citation
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Results Reference
result

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Water And Saline Head-to-head In The Blinded Evaluation Study Trial

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