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Evaluation of the therapeutic effect of crocin along with standard regimes in colorectal cancer

Evaluation of the therapeutic effect of crocin along with standard regimes in patients with colorectal cancer, A double blind randomized controlled trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20131017015044N2
Enrollment
100
Registered
2020-01-12
Start date
2019-12-22
Completion date
Unknown
Last updated
2020-02-24

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 rectosigmoid junction

Interventions

Intervention 1: Intervention group: Crocin along with standard regime will be assigned to intervention group. The daily dose of crocin will be 30 mg (two 15 mg tablets) during 12 weeks. Intervention 2

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 75 Years

Inclusion criteria

Inclusion criteria: Colorectal cancer patients with lung or liver metastasis or both that is measurable Colorectal cancer patients who have not received any chemotherapy for metastasis

Exclusion criteria

Exclusion criteria: History of any allergy to saffron or its products

Design outcomes

Primary

MeasureTime frame
Overall survival. Timepoint: One year after the treatment is completed. Method of measurement: Patient follow-up.

Secondary

MeasureTime frame
Progression-free survival. Timepoint: During treatment and after it every 3 months. Method of measurement: criteria of Response evaluation criteria in solid tumors.;Anemia. Timepoint: Before each session of monthly chemotherapy. Method of measurement: laboratory assessment of complete blood count.;Neutropenia. Timepoint: Before each session of monthly chemotherapy. Method of measurement: laboratory assessment of complete blood count.;Thrombocytopenia. Timepoint: Before each session of monthly chemotherapy. Method of measurement: laboratory assessment of complete blood count.;Kidney function. Timepoint: Before each session of monthly chemotherapy. Method of measurement: laboratory assessment of BUN and creatinine.;Liver function. Timepoint: Before each session of monthly chemotherapy. Method of measurement: laboratory assessment of SGOT and SGPT.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSoodabeh Shahidsales

Mashhad University of Medical Sciences

Shahidsaless@mums.ac.ir+98 51 3846 1518

Outcome results

None listed

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