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Effect of Pentoxifylline treatment on quality of life and change in arm circumference compared to placebo in patients with cancer cachexia: A double-blind, randomized, placebo-controlled trial

Effect of Pentoxifylline treatment on quality of life and change in arm circumference compared to placebo in patients with cancer cachexia: A double-blind, randomized, placebo-controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013081410297N2
Enrollment
70
Registered
2013-11-23
Start date
2011-10-15
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

Malignant neoplasm. Malignant neoplasm, without specification of site

Interventions

Intervention 1: Intervention group will receive Pentoxifylline (400 mg) three times a day. Intervention 2: Control group will receive exactly similar placebo capsules regarding shape, size and taste.
Treatment - Drugs
Placebo
Intervention group will receive Pentoxifylline (400 mg) three times a day.
Control group will receive exactly similar placebo capsules regarding shape, size and taste.

Sponsors

Vice chancellor for research, Isfahan University of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria are: 1. Histologic or cytologic proof evidencing cancers, 2. Incurable malignancy with a life expectancy=4 months, 3. Weight loss perceived by the patient as a problem, 4. Patient should be alert and mentally competent. Exclusion criteria are: 1. Affliction with edema or ascites, 2. Adrenal corticosteroids treatment (except for dexamethasone during chemotherapy) androgens, progestational agents, or other appetite stimulants within the previous month, 3. Brain metastases, 4. Pregnancy or lactation, 5. Mechanical obstruction of the alimentary tract, 6. Malabsorption, or intractable vomiting, 7. Poorly controlled hypertension or congestive heart failure.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Arm circumference. Timepoint: before and two months after intervention. Method of measurement: Meter calibrated.;Quality of life. Timepoint: before and two months after intervention. Method of measurement: SF-36 standard questionnaire.

Secondary

MeasureTime frame
Side effects. Timepoint: during treatment. Method of measurement: clinical observation (nausea / vomiting / tachycardia).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactValiollah Mehrzad

Isfahan University of Medical Sciences

valimehrzad@yahoo.com+98 31 1668 5555

Outcome results

None listed

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