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effect of Pentoxifylline on fatigue and sleep disturbances in Cirrhosis

Preliminary study of the efficacy and safety of Pentoxifylline in addressing fatigue and sleep disturbances among individuals with cirrhosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20121021011192N21
Enrollment
30
Registered
2025-10-26
Start date
2025-12-22
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Liver Cirrhosis. Other and Unspecified cirrhosis of liver

Interventions

Intervention 1: Intervention group: Participants in the intervention group will receive Pentoxifylline 400 mg tablets (Amin Pharmaceutical Co., Iran).Pentoxifylline is a methylxanthine derivative with

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Adults (=18 years) with cirrhosis and fatigue symptoms Willingness to participate and provide informed consent. Fatigue Severity Scale (FSS) equal and greater than 28 patients with Cirrhosis child pugh score A and B

Exclusion criteria

Exclusion criteria: patients with Cirrhosis child pugh score C Known allergy to Pentoxifylline or xanthine derivatives Recent cerebral or retinal hemorrhage Significant drug interactions (e.g., warfarin, theophylline)

Design outcomes

Primary

MeasureTime frame
Fatigue Severity. Timepoint: before intervention and 30 days after intervention. Method of measurement: Fatigue Severity Scale (FSS).;Quality of Sleep. Timepoint: before intervention and 30 days after intervention. Method of measurement: Pittsburgh Sleep Quality Index.

Secondary

MeasureTime frame
TNF Alpha Serum Level. Timepoint: before intervention and 30 days after intervention. Method of measurement: Elisa 96-test kit.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Abbasinazari

Shahid Beheshti University of Medical Sciences

m_abbasi@sbmu.ac.ir+98 21 8820 0118

Outcome results

None listed

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