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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05528003
Other study ID # 202104032RINB
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 1, 2013
Est. completion date April 30, 2022

Study information

Verified date August 2022
Source National Taiwan University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Homemade and commercialized single-assess port devices are two kinds of port devices commonly used for single-incision laparoscopic appendectomy. This study aimed to compare these two port devices in terms of short-term surgical outcomes and medical costs.


Description:

The advantages of homemade port devices include accessibility of the composites and lower equipment costs to the patients; however, the potential disadvantage is the easy leakage of CO2, ballooning of the surgical glove, and device instability, leading to difficult maneuverability. On the other hand, commercialized port devices have relatively easy maneuverability, flexibility for instrument changes, and port stability for long-duration surgery ; however, their higher equipment cost is a disadvantage.


Recruitment information / eligibility

Status Completed
Enrollment 161
Est. completion date April 30, 2022
Est. primary completion date April 30, 2022
Accepts healthy volunteers No
Gender All
Age group 9 Years and older
Eligibility Inclusion Criteria: - The patients were diagnosed as acute appendicitis and undergoing single-incision laparoscopic appendectomy Exclusion Criteria: - The patient was not diagnosed as acute appendicitis based on surgical finding or pathological findings - The patients underwent surgery other than single-incision laparoscopic surgery

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Commercialized single-access port devices
Two kinds of commercialized single-access port devices were used.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
National Taiwan University Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Total surgical complications Complications were defined by Clavien-Dindo classification and comprehensive complication index. Complications happened within 30 days
Primary Superficial incisional surgical site infection (SSI) SSI was defined according to the American Centers for Disease Control and Prevention (CDC) classification Complications happened within 30 days
Primary Deep/organ SSI SSI was defined according to the American Centers for Disease Control and Prevention (CDC) classification Complications happened within 30 days
Primary Postoperative ileus Postoperative ileus was defined as the presence of symptoms and signs of abdominal distention, nausea, or vomiting combined with abdominal radiography, such as plain radiography or CT, within 30 days after SILA. Complications happened within 30 days
Secondary Surgical time Total time needed for completing surgery Time from skin incision to application of gauzes
Secondary Time to resume soft diet Total time needed to resume bowel ability to resuming soft diet The time to resume a soft diet was measured as the duration between the time leaving the recovery room and the time to resume a soft diet recorded in the nursing note.
Secondary Postoperative length of hospitalization Total time to stay in hospital Postoperative LOH was defined as the duration between leaving the recovery room and discharge.
Secondary Total medical costs Medical costs were defined as the medical fees paid by the National Health Insurance and did not include the self-paid equipment fees needed in SILA (e.g., commercialized single-access port devices, or wound protector). From the time patient being brought to emergency room to the time patient being discharged
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