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Clinical Trial Details — Status: Suspended

Administrative data

NCT number NCT03990974
Other study ID # 20190236
Secondary ID
Status Suspended
Phase Phase 3
First received
Last updated
Start date September 2020
Est. completion date July 2021

Study information

Verified date March 2020
Source Sun Yat-sen University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This trial is a multi-center, double-blinded, randomized (1:1) clinical trial. The aim is to compare the postoperative infection rate between the 3 days postoperative AMP group and the placebo group in HCC patients undergoing hepatectomy.


Description:

This trial includes two phase. The first phase is the internal pilot study to explore the expulsion rate and recruited population. The second phase is the main phase III trial.


Recruitment information / eligibility

Status Suspended
Enrollment 458
Est. completion date July 2021
Est. primary completion date June 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Age: over 18 years;

- Diagnosed as primary HCC according to the EASL criteria and plan to receive hepatectomy;

- Child-Pugh A class;

- No history of antibiotics in 1 week before surgery, except for antimicrobial prophylaxis in the 24h before surgery.

- No evidence of infection during preoperational assessment

Exclusion Criteria:

- Underwent hepatectomy combined with resection of other organs, except for gallbladder;

- Found obvious infection during operation;

- Combination with other operations, such as biliary reconstruction or tube drainage, bile duct exploration and stone remove, etc.;

- Allergic to the antibiotics used in the 24h before surgery;

- Emergency surgery;

- Tumor rupture;

- Did not underwent hepatectomy because of any reasons;

- Admission to ICU after surgery;

- ASA grade = 3;

- Denial of informed consent.

Study Design


Intervention

Drug:
postoperative antimicrobial prophylaxis
The drugs are all common antibiotics used to prevent postoperative infection in each hospital.
Other:
No postoperative antimicrobial prophylaxis
Patients will receive no antibiotics after hepatectomy unless necessary.

Locations

Country Name City State
China The First Affiliated Hospital of Sun Yat-sen University Guangzhou Guangdong

Sponsors (1)

Lead Sponsor Collaborator
Sun Yat-sen University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary 30-day postoperative infection rate the incidence rate of postoperative infection occurred in 30 days after surgery, including surgical site infections, distant infection or infection from unknown sources 30 days after hepatectomy
Secondary Surgical site infection rate the incidence rate of surgical site infection, including infections of the incision or organ or space that occur after surgery. 30 days after hepatectomy
Secondary Postoperative complication rate the incidence rate of postoperative complications, grading as Clavien-Dindo grades 3 months after hepatectomy
Secondary Severe infection rate the incidence rate of postoperative complications over grade 3 30 days after hepatectomy
Secondary Distant infection rate the incidence rate of distant infections, including respiratory system infection, urinary system infection, catheter related infections or sepsis (defined as fever (temperature =38 ?) or elevated white blood cell (> 10 x10^9 / L) accompanied by sputum, urine, catheter secretions, or blood culture positive. 30 days after hepatectomy
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