Clinical trial · Interventional
The Combination Effect of Statin Plus Metformin on Relapse-free
NCT02819869CI-TRIAL-00027062terminatedPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): insufficient for the fund
Summary
Brief summary (as posted)
The study demonstrated that either statin or metformin served as notable use in reducing the incidence of many cancers.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Hepatocellular Carcinoma | Hepatocellular Carcinoma | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Statin and Metformin use | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Taking both statin and metformin Group
- description
- The experimental group take Lotidon 500mg/ tablet per day and Lipitor 10mg/ tablet per day for two years or until of a recurrence.
- interventionNames
- Drug: Statin and Metformin use
- type
- NO_INTERVENTION
- label
- Non- taking both statin and metformin Group
- description
- Non- taking both statin and metformin.
Primary outcomes (1)
- measure
- relapse-free survival of hepatocellular carcinoma patients
- timeFrame
- Up to 2 years
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 20 Years
Show eligibility criteria text
Inclusion Criteria:
* 1\. 20 years or older at the time of obtaining consent. 2. Systemic conditions are 0 to 2 score of Performance Status (according to Eastern Cooperative Oncology Group: ECOG). 3.Diagnosis of hepatocellular carcinoma is based on the following 1) or 2).
1. Patients who are confirmed to have early tumor stain and typical finding(s) of hepatocellular carcinoma with CT or MRI imaging
2. Patients who underwent tumor biopsy and are histopathologically diagnosed as hepatocellular carcinoma 4. First onset or recurrence of hepatocellular carcinoma is not more than 1 time.
5\. Patients who underwent the following 1) or 2) prior to registration to determine therapeutic effect.
1. Patients who underwent local therapy to achieve complete hepatonecrosis and are confirmed to have complete hepatonecrosis with CT imaging or MRI.
2. Patients who underwent surgical treatment(s) and are confirmed not to have residual tumor with CT or MRI imaging. 6. Patients who are given full explanation of study participation (including cancer notification) and submit written consent forms with their understanding as well as voluntary will for this study.
Exclusion Criteria:
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1. Hepatocellular carcinoma: 1) Patients who have extrahepatic metastasis 2) Patients who have portal invasion 3) Patients who experienced with systemic administration of anti-malignant tumor drugs to treat hepatocellular carcinoma
2. Patients with encephalopathy in which pharmacotherapy is ineffective
3. Patients with ascites or pleural effusion that cannot be managed with diuretics
4. Systemic conditions:
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1. Patients unable to receive oral administration
2. Patients with a history of gastrectomy or extensive resection of digestive tract
3. Patients who are suspected to have biliary occlusion, choleretic disorder,cholecystectomy, or malabsorption of liposoluble agents
4. Patients with multiple cancers (within a 5-year cancer-free period \[from the same day of 5 years earlier to the day of obtaining consent forms) 5. Drug administration:
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1. Patients on warfarin therapy
2. Patients who already use statin or metformin 6.Other exclusion criteria
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1. Women of pregnant, lactating, childbearing potential, or with the intention of becoming pregnant
2. Patients who are presently participating in another clinical study (except for follow-up surveys for study outcomes)
3. Patients who are judged to be ineligible for study entry by the investigator or subinvestigator
4. GOT or GPT three times greater than normal
5. Cr. 1.5 times greater than normal
6. Child-pugh score CReferences
Publications (0)
Data not yet available
No reference posted for this study.