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Evaluation of the Effect of ACA1 on Gastric adenocarcinoma:

Evaluation of the Effect of ACA1 on the Quality of Life in Patients with Gastric adenocarcinoma: a pilot study

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200626047927N1
Enrollment
20
Registered
2020-07-11
Start date
2020-07-22
Completion date
Unknown
Last updated
2020-08-17

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

Conditions

Gastric adenocarcinoma. Malignant neoplasm of stomach

Interventions

Intervention 1: Intervention group: This group was treated with ACA1 capsules for 2100 mg per day for one month. Intervention 2: Control group: This group is treated with placebo capsules three times

Sponsors

Shahed University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with gastric adenocarcinoma whose disease has been confirmed histologically, are in the metastatic stage and at least two common chemotherapy treatments have been administered to them and the disease is not under control. Adequate bone marrow function: 40001500, Plt>100000, Hb>8 Adequate liver function: Total Bill>1.5, AST&ALT<100 Adequate kidney function: Cr<1.5 performance status=1

Exclusion criteria

Exclusion criteria: positive serology for HIV, HBV, HCV Metastasis to CNS other malignancies

Design outcomes

Primary

MeasureTime frame
Quality of Life. Timepoint: Start of study (before the start of the intervention) and one month after the start of ACA1 consumption. Method of measurement: EORTC-QLQ-30 Standard questionnaire.

Secondary

MeasureTime frame
White Blood Cell Count. Timepoint: Start studying (before starting the intervention) and one month after starting ACA1 consumption. Method of measurement: Cell Counter.;Hemoglobin. Timepoint: Start studying (before starting the intervention) and one month after starting ACA1 consumption. Method of measurement: Cell Counter.;Platelet Count. Timepoint: Start studying (before starting the intervention) and one month after starting ACA1 consumption. Method of measurement: Cell Counter.;Body Mass Index. Timepoint: Start studying (before starting the intervention) and one month after starting ACA1 consumption. Method of measurement: Meter and scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Sharifan

Shahed University

z.Sharifan@shahed.ac.ir+98 21 2257 2759

Outcome results

None listed

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