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Celecoxib prevents postoperative fever in hepatocellular carcinoma patients receiving transcatheter arterial chemoembolization: a prospective randomized trial

Celecoxib prevents postoperative fever in hepatocellular carcinoma patients receiving transcatheter arterial chemoembolization: a prospective randomized trial

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-17010323
Enrollment
Unknown
Registered
2017-01-04
Start date
2017-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Hepatocellular carcinoma

Interventions

Intervention group:Celecoxib fever after hepatic artery embolization for Celecoxib was used for fever after hepatic artery embolization with hepatocellular carcinoma
control group:none

Sponsors

Lishui Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Aged from 18 to 80 years; (2) Diagnosed with HCC based on the criteria established by the American Association for the Study of Liver Diseases (AASLD); (3) Inoperable HCC; the nodule size is greater than 3 cm; (4) Without radiotherapy, chemotherapy and molecular targeted therapy in a month; (5) Main portal vein without clogging, or occlusion but the formation of collateral vessels; (6) had a Karnofsky Performance Status (KPS) score =70; (7) stage A or B HCC according to the Barcelona Clinic Liver Cancer (BCLC) staging classification.

Exclusion criteria

Exclusion criteria: (1) a history of serious allergic reactions to medicines, pregnancy or breastfeeding women; (2) heart failure, severe hepatic and renal dysfunction; (3) hypersensitivity to celecoxib; (4) white blood cell counts (WBCs)<4.0×10^9/L, platelets <50×10^9/L; (5) Coagulation defects; (6) Intrahepatic arteriovenous fistula; (7) Obvious pleural effusion and ascites; (8) gastrointestinal hemorrhage in the last 6 months.

Design outcomes

Primary

MeasureTime frame
Quality of life;Safety;

Secondary

MeasureTime frame
post-operative complication;progression free survival;Immune status;

Countries

China

Contacts

Public ContactJiansong Ji

Lishui Central Hospital

jjstcty@sina.com+86 13857088508

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026