Skip to content

Determination of Apium graveolens l.fruit effect in patient with colorectal cancer.

Determination of Apium graveolens l.fruit effect on folfox induced neuropathy in patient with colorectal cancer.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017030818828N2
Enrollment
66
Registered
2017-04-18
Start date
2017-04-21
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

colorectal cancer. Malignant neoplasm of colon

Interventions

Intervention 1: Patients in main group received standardized capsules containing in Apium graveolens L.fruit for 12 courses daily with 8h spans. They were informed of consumption instructions and tim
Treatment - Drugs
Placebo
Patients in main group received standardized capsules containing in Apium graveolens L.fruit for 12 courses daily with 8h spans. They were informed of consumption instructions and time. Patients were
Patients in main group received standardized capsules containing in cellulose for 12 courses daily with 8h spans. They were informed of consumption instructions and time.

Sponsors

Yazd University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: Enclusion criteria: Patient must be suffering from colorectal cancer; Patient must be between 20 to 80 years old; The patient must have received folfox diet containing folinic acid; 5-fluro uracil and oxaliplatin; Full satisfaction of the patient Exclusion criteria: Patients who take acupuncture during their treatment; Patients who receive massage therapy during their treatment; Patients who receive physiotherapy during their treatment; Patients who take indigenous medicine; Patients with previously-diagnosed neuropathy; Patients with lupus or rheumatoid arteritis; Patients with other forms of cancer

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The pain. Timepoint: Beforetreatment, 5 to 6 months after treatment. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAlimohamad Ranjbar Jamal abadi

Yazd University of Medical Sciences

amranjbar@razi.tums.ac.ir+98 35 3820 3409

Outcome results

None listed

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