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Irrigation Versus Suction in Complicated Acute Appendicitis

Randomized Trial Comparing Irrigation Versus Suction in Laparoscopic Appendectomy for Complicated Acute Appendicitis in Adults

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02688244
Acronym
ISAAC
Enrollment
210
Registered
2016-02-23
Start date
2015-11-30
Completion date
2017-10-31
Last updated
2016-02-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Appendicitis, Abdominal Abscess, Acute Disease, Cecal Diseases, Infection

Keywords

complicated appendicitis, laparoscopic appendectomy, irrigation, suction, abdominal abscess

Brief summary

This study evaluates the intraabdominal abscess rate after laparoscopic appendectomy in complicated acute appendicitis performing irrigation of the abdominal cavity or only suction without lavage.

Detailed description

Despite the available literature for and against the irrigation of the abdominal cavity in complicated acute appendicitis, in the current practice of this and other centres, the irrigation and no irrigation is made equally depending on the surgeon who performs the intervention. Those who systematically irrigate the abdominal cavity in laparoscopic appendectomies do it as an inherited act from open surgery and those who systematically do not irrigate the abdominal cavity base their choice in theories such as abscess migration due to the irrigation and difficulty of the suction of all the irrigated fluid, spreading, therefore, the infection. The intention of the investigators is to provide evidence about this technique in order to either systematize peritoneal irrigation in laparoscopic appendectomy for complicated appendicitis or avoid an unnecessary gesture, if it were established so. This will be a prospective, randomized clinical trial involving patients who present to the hospital with complicated acute appendicitis. Power calculation was based on abscess rate in the investigators' hospital calculated retrospectively (15%) Subjects will be those patients above 18 y.o. who are found to have complicated acute appendicitis (defined as perforated appendicitis before or during surgery, gangrenous appendicitis and/or purulent peritonitis). The final decision to include a patient in the study will made after complication has been visually confirmed during surgery. The randomization assignment will be made known at the initiation of the operation, and confirmation of complication will confirm the patient will utilize the next randomization slot. The irrigation group will have suction irrigator set up with a 1 liter bag of normal saline. The surgeon must use at least 300 ml of this bag but may use as much as they choose. The no irrigation group will have the suction irrigator set up without the saline attachment. This will leave them with the capacity for suction only. Since several suction devices exist, this will assure the same type of suction for both groups. After the operation, both groups will be managed in the same manner. When the patient is tolerating a regular diet, on oral pain medication and has been afebrile for over 12 hours, they will be discharged on oral antibiotics to complete a course of 7 days. If the participants stay until the 5th post-operative day, a white blood cell count will be checked, which if it is normal, they will be discharged to home without antibiotics.

Interventions

PROCEDUREIrrigation

Irrigation of the abdominal cavity with at least 300ml of normal saline using the power suction/irrigator

PROCEDURENo irrigation

Suction only, using suction device

Sponsors

Hospital Universitario Virgen de la Arrixaca
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with complicated acute appendiccitis * Laparoscopic approach

Exclusion criteria

* Open approach * Medical or psychiatric condition of the patient that compromises the informed consent authorisation * Non complicated acute appendicitis * Underage patients (\<18) * Refusal to participate in the study.

Design outcomes

Primary

MeasureTime frameDescription
Incidence of post-operative abscess1 monthNumber of post-operative abscesses in each arm
Location of post-operative abscessOne monthNumber of abscesses in every quadrant of the abdomen
Treatment of post-operative abscessOne monthNumber of post-operative abscesses treated with a radiological drain

Secondary

MeasureTime frameDescription
Postoperative pain (Visual analogic scale)6 daysVisual analogic scale, from 1 to 10
Postoperatory fever6 daysBody temperature in Celsius degrees
Operating time1 dayLength of surgery, in minutes.
Hospital stay (Time until discharge)2 weeksTime until discharge, in days.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026