Skip to content

"Evaluation of the effect of chamomile in Parkinson's patients"

The effect of chamomile extract on motor function and quality of life in patients with Parkinson disease

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220421054601N1
Enrollment
50
Registered
2022-05-30
Start date
2022-05-31
Completion date
Unknown
Last updated
2022-06-27

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

Conditions

Parkinson. Parkinson's disease

Interventions

Intervention 1: Intervention group: Chamomile capsules (200 mg) will be taken twice a day (morning and night) for 28 consecutive days. The dose of chamomile was considered with the advice of a pharmac

Sponsors

Kashan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: No allergies to chamomile or its derivatives Ability to communicate verbally and respond to study tools Dont use anticoagulants (such as heparin, warfarin, aspirin and Plavix) Non-dependence on drugs (including drugs, alcohol, painkillers, antidepressants and hypnotics) No asthma, cancer, insulin-dependent diabetes mellitus and systemic lupus erythematosus, heart failure and mental, hepatic or renal disorders, no use of anticoagulants (heparin, warfarin, aspirin and Plavix), no use of hypnotics And drugs. (Because the capsule used in this study is herbal, it may interfere with drugs with chemical compounds.)

Exclusion criteria

Exclusion criteria: Reluctance of the patient to continue cooperation Non-continuous use of medication as prescribed The occurrence of allergies in the patient The patient should stop consuming chamomile extract for any reason before the end of the intervention period

Design outcomes

Primary

MeasureTime frame
Motor function. Timepoint: Before taking the capsules and 28 days after taking the capsules daily. Method of measurement: check list: Short Parkinson's Evaluation Scale/Scales for Outcomes in Parkinson’s Disease – Motor Function.

Secondary

MeasureTime frame
Quality of Life. Timepoint: Before taking the capsules and 28 days after taking the capsules daily. Method of measurement: Quality of Life Questionnaire in Parkinson's Patients (PDQ-39).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Seyed Ali Masoud

Kashan University of Medical Sciences

masoud_s_a@yahoo.com+98 31 5545 6645

Outcome results

None listed

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