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he effect of ginseng on cancer related pain, and Quality of sleep

he effect of ginseng on cancer related pain, and Quality of sleep in cancer survivors: a clinical trial study.

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171015036777N2
Enrollment
80
Registered
2018-01-10
Start date
2018-02-04
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

cancer. Neoplasm related pain (acute) (chronic)

Interventions

Intervention 1: Intervention group: Standard Jensing Extract 250 mg, Gol daru Factory, once a day. Intervention 2: Control group: Capsules of the same color and shape and size with the main drug fille
Treatment - Drugs
Placebo
Intervention group: Standard Jensing Extract 250 mg, Gol daru Factory, once a day
Control group: Capsules of the same color and shape and size with the main drug filled with placebo (wheat flour)

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: A definitive diagnosis of cancer according to the opinion of the oncologist Patients who are at stage II and I of the disease. Patients with colorectal cancer or stomach cancer Having a sleep disorder Having pain

Exclusion criteria

Exclusion criteria: Use of anesthetics and narcotic drugs during study Participant's unwillingness to continue participating in the study Mental illness that is mentioned in the medical history of the patient. Receiving sleep disturbances such as diuretic drugs, antidepressants, inotropes and amphetamines at night Need for cardiopulmonary resuscitation during the intervention Mental disabilities Taking anti-coagulant drugs such as warfarin or aspirin Having diabetes and receiving anti-diabetes treatment

Design outcomes

Primary

MeasureTime frame
Pain based on scale vas. Timepoint: Before the intervention, 30 days after the intervention. Method of measurement: scale VAS.

Secondary

MeasureTime frame
Sleep quality based on Pittsburgh scale. Timepoint: Before the intervention, 30 days after the intervention. Method of measurement: Pittsburgh scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAzad Rahmani

Tabriz University of Medical Sciences

nursing@tbzmed.ac.ir+98 41 3479 6770

Outcome results

None listed

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