Hepatocellular Carcinoma
Conditions
Brief summary
This study is aiming to understand the effects of parecoxib on the postoperative complications of hepatocellular carcinoma (HCC) patients undergoing hepatic transcatheter arterial embolization (TACE). The investigators enrolled 242 patients who were diagnosed with HCC for the first time and who received hepatic TACE at the Cancer Prevention and Treatment Center of Sun Yat-sen University from October 2014 to March 2015 were prospectively enrolled. The patients were divided into study and control groups according to whether parecoxib sodium was administered postoperatively. Pain scores,body temperature, vomiting, and changes in liver function after surgery, as well as the length of the hospital stay, were recorded and compared.
Interventions
DRUGparecoxib sodium
parecoxib sodium was administered postoperatively, when transcatheter arterial embolization finished.
Sponsors
Sun Yat-sen University
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
1. Diagnosed with HCC according to the primary liver cancer diagnosis and treatment practices published by theMinistry of Health in 2011 2. A previous history of hepatitis B or positivity for hepatitis B surface antigen (HBsAg) 3. A Karnofsky Performance Status (KPS) score ≥70 points 4. Age between 18 and 65 years 5. Child-Pugh classA or B (class B patients had scores no greater than 7 points). In addition, the baseline laboratory tests had to meet the following criteria: white blood cells (WBCs) ≥1.5 × 109/L, platelets ≥50 × 109/L, hemoglobin ≥80 g/L, serum aspartate transaminase (AST) and alanine transaminase (ALT) ≤ 2 x the upper limit of normal (ULN), serum creatinine ≤ 1.5 x ULN, an international normalized ratio (INR)\<1.5 or prothrombin time \< the ULN + 4 seconds, albumin ≥30 g/L, and total bilirubin ≤34mmol/L
Exclusion criteria
1\. Patients who had iodine allergies, severe heart and lung diseases, significant fever or pain, or continuous use of anti-inflammatory drugs within the past three months were excluded
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Pain scores | 3 days after TACE | VAS pain scores recorded after TACE |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Body temperature | 3 Days after TACE | The maximum daily temperature at each of the time points were recorded before TACE,two hours postoperative, and the first, second, and third postoperative days, respectively. |
| Liver function | 2 days after TACE | Before and after TACE to compare |
| Hospital Stay | within 3 days after discharge | — |
Outcome results
None listed