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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01967745
Other study ID # 01091981
Secondary ID
Status Completed
Phase N/A
First received October 11, 2013
Last updated October 22, 2014
Start date January 2007
Est. completion date September 2013

Study information

Verified date October 2014
Source Varazdin General Hospital
Contact n/a
Is FDA regulated No
Health authority Croatia: Ethics Committee
Study type Observational

Clinical Trial Summary

Comparison of open and laparoscopic appendectomy


Description:

Adult patients with presumptive diagnosis of acute appendicitis were were operated by laparoscopic appendectomy or open appendectomy group during a three-year period (between 2007 and 2009).


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date September 2013
Est. primary completion date December 2009
Accepts healthy volunteers No
Gender Both
Age group 16 Years to 90 Years
Eligibility Inclusion Criteria:

- patients older than 16 years with presumptive diagnosis of acute appendicitis

Exclusion Criteria:Appendectomy performed during diagnostic laparoscopy and incidental appendectomies patients with:

- cirrhosis

- ascites

- coagulation disorder

- diffuse peritonitis

- shock on admission

- large ventral hernia. Appendectomy performed during diagnostic laparoscopy and incidental appendectomies were also excluded

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Intervention

Procedure:
laparoscopic appendectomy
The laparoscopic appendectomy was performed with three trocars. Pneumoperitoneum was created using an open Hasson technique. The mesoappendix was divided using a harmonic scalpel or endoscopic tissue fusion device. The appendix was divided by placing one endoscopic loop and cut with harmonic scalpel. The specimen was removed through the umbilical port.
open appendectomy
The open appendectomy was carried out in the standard way with McBurney muscle splitting incision (in supine position).

Locations

Country Name City State
Croatia Varazdin General Hospital Varazdin

Sponsors (1)

Lead Sponsor Collaborator
Varazdin General Hospital

Country where clinical trial is conducted

Croatia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Cost of hospitalization based on the final hospital bills from the beginning of the surgery till discharge from hospital (an expected average of 8 days, maximmum 20 days) No
Secondary Analgesia demands The number of doses of analgesics, and time from surgery to the last dose of analgesics. from the beginning of the surgery till discharge from hospital (an expected average of 8 days, maximmum 20 days) No
Secondary Complications No. of wound infection and intrabdominal abscesses. during first 4 weeks after the surgery No
Secondary Length of hospital stay No. of days from surgery to discharge of hospital from the beginning of the surgery till discharge from hospital (an expected average of 8 days, maximmum 20 days) No
Secondary Time until resumption of clear liquid and regular diet No. of days from surgery to the resumption of clear liquid and regular diet from the beginning of the surgery to the resumption (an expected average 2 days after the surgery) No
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