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Determining the efficacy of Iscador in cancer

Determining the efficacy of Iscador in quality of life of patients with stage 4 gastric or pancreas cancer

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20080901001165N66
Enrollment
80
Registered
2021-11-28
Start date
2021-11-22
Completion date
Unknown
Last updated
2022-01-11

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

Conditions

Gastrointestinal cancer. Malignant neoplasm of stomach

Interventions

Intervention group: Mistletoe extract(Iscador Qu) s.c., applied three times weekly on day 2, 4 and 6 after chemotherapy between 7:00 and 9:00 a.m.The maximum applied dose will be determined by titrati

Sponsors

Avicenna-MC
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age: 18 to 80 years Voluntary written informed consent given prior to inclusion in this clinical trial Histologically confirmed (without T0, Tis, T1mic) invasive stage 4 adenocarcinoma of the stomach or pancreas

Exclusion criteria

Exclusion criteria: Assured allergy to mistletoe-containing products Co-morbidity with one of the following: hyperthyroidism and autoimmune diseases Current or during last 6 month use of immunostimulant or immunosuppressive agents except therapeutics within the routinely administered standard therapy Pregnancy or breast feeding

Design outcomes

Primary

MeasureTime frame
Quality of life assessed by EORTC QLQ-C30 questionnaire. Timepoint: Month 0 (baseline) then monthly for 6 month. Method of measurement: EORTC QLQ-C30 questionnaire.

Secondary

MeasureTime frame
Effects of Iscador in tumor progression. Timepoint: Assessed at screening and after 6 month of therapy. Method of measurement: Computer-tomography according to RECIST criteria.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHamidreza Jalalian

Bagheiat-allah University of Medical Sciences

hamidreza.jalalian@yahoo.com+98 21 8126 3988

Outcome results

None listed

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