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Effect of Aspirin and Atorvastatin on liver function in patients with hepatic failure

The effect of combination therapy with Atorvastatin and Aspirin on the severity of fibrosis and liver function in compensated cryptogenic cirrhosis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016120531252N1
Enrollment
40
Registered
2017-02-28
Start date
2017-01-20
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Liver Cirhhosis. Chronic hepatic failure

Interventions

Intervention 1: Atorvastatin, tab 20 mg oral, once daily, for 6 months along with ?Asprin, tab 80 mg Oral, once daily, for six months. Intervention 2: Atorvastatin, tab 20 mg, oral, once daily, for 6
Treatment - Drugs
Placebo
Atorvastatin, tab 20 mg oral, once daily, for 6 months along with ?Asprin, tab 80 mg Oral, once daily, for six months
Atorvastatin, tab 20 mg, oral, once daily, for 6 months along with placebo (of Aspirin), Oral, once daily, for 6 months

Sponsors

Office of Research & Technology, Qom University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients with compensated cryptogenic cirrhosis; living in Qom; Age of 18 to 75 years; patient without another type of cirrhosis; who have not been treated with statins; patients with serum LDL>70; Patients with PLT>50000 Exclusion criteria: Increased liver enzymes more than three times, three months after treatment; Lack of cooperation in the proper use of drugs; Statin-induced myopathy; use of Fibrates, Erythromycin, and other drugs that suppressed metabolism of p450 liver enzyme

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Sevirity of fibrosis. Timepoint: six months after begining intervention. Method of measurement: kpa with fibroscan.;Liver function. Timepoint: six months after begining intervention. Method of measurement: child score.

Secondary

MeasureTime frame
Liver enzymes levels. Timepoint: six month after begining of intervention. Method of measurement: IU/L.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMansoureh Molaei

Qom University of Medical Sciences

Mansourehmolaei@ymail.com; Mahdijahangiry@yahoo.com+98 256122053

Outcome results

None listed

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