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The effectiveness of Lavandula stoechas in Parkinson's disease

The efficacy of Lavandula stoechas product on motor symptoms of patients with Parkinson's disease treated with levodopa : A double-blind clinical trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230505058093N1
Enrollment
30
Registered
2024-05-17
Start date
2023-12-22
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Parkinson's disease. Parkinson's disease

Interventions

Intervention 1: Intervention group: This group receives the standard treatment of levodopa (levodopa/carbidopa tablet three times daily)along with lavender capsules for 8 weeks. The dose of the drug

Sponsors

Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
55 Years to 75 Years

Inclusion criteria

Inclusion criteria: Idiopathic Parkinson's disease Age range of 55 to 75 years The onset age of the disease is less than 5 years Stages one to three of Parkinson's disease

Exclusion criteria

Exclusion criteria: The lack of physical and mental ability to answer the questions Alcohol and drug use History of systemic physical diseases such as diabetes, heart and brain stroke, heart, respiratory and kidney failure and uncontrolled blood pressure Occurrence of debilitating disease during treatment Taking a new drug due to lack of response to levodopa treatment or intolerance to levodopa if the diagnosis is primary Taking sedative drugs or drugs that interfere with lavender, such as antipsychotic drugs, monoamine oxidase inhibitors, benzodiazepines, tricyclic antidepressants, anticonvulsants, and barbiturates.

Design outcomes

Primary

MeasureTime frame
Movement signs. Timepoint: Patients are examined at the beginning of the study, week 4, week 8 and 4 weeks after stopping the drug (week 12). Method of measurement: The SPES/SCOPA questionnaire is completed by the attending physician in four stages during the treatment period.

Secondary

MeasureTime frame
Daily activities. Timepoint: Patients are examined at the beginning of the study, week 4, week 8 and 4 weeks after stopping the drug (week 12). Method of measurement: Specific Parkinson's Quality of Life Questionnaire (PDQL).;Quality of Life. Timepoint: Patients are examined at the beginning of the study, week 4, week 8 and 4 weeks after stopping the drug (week 12). Method of measurement: Specific Parkinson's Quality of Life Questionnaire (PDQL).;Motor complications. Timepoint: Patients are examined at the beginning of the study, week 4, week 8 and 4 weeks after stopping the drug (week 12). Method of measurement: Specific Parkinson's Quality of Life Questionnaire (PDQL).;Changing position. Timepoint: Patients are examined at the beginning of the study, week 4, week 8 and 4 weeks after stopping the drug (week 12). Method of measurement: Specific Parkinson's Quality of Life Questionnaire (PDQL).

Countries

Iran (Islamic Republic of)

Contacts

Public Contactreihaneh mirshekari

Kerman University of Medical Sciences

reihaneh.mirshekari@gmail.com+98 34 3244 1504

Outcome results

None listed

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