Effects of an herbal supplement on quality of life in patients with gastrointestinal cancers

Phase 1

Recruiting

• Conditions: Cancers of oesophagus and stomach.; Oesophagus, unspecified; Stomach, unspecified; C15.9 and

• Registration Number: IRCT2017030416776N2
• Lead Sponsor: Mashhad University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

Patients with cancers of esophagus or stomach; Normal liver enzymes; Hb more than 9 g/dL; Platelet more than 100000; Creatinine less than 1.5 mg/dl.
Exclusion criteria: Patients with severe complication of cancer; Induction of toxicity by the herbal supplement; Pregnancy; Consumption of anticoagulant drugs

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Quality of life. Timepoint: 30 days and 60 days after beginning of study. Method of measurement: Questionnaire.