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The evaluation of the topical effect of Chamomile Oil on improving neuropathy symptoms

The evaluation of the topical effect of Chamomile Oil on improving neuropathy symptoms in controlleddiabetic patients attend Shiraz diabetes clinic in 2022 A randomized double-blinded controlled clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240611062090N1
Enrollment
72
Registered
2024-08-06
Start date
2024-08-05
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

Diabetic Neuropathy. Type 2 diabetes mellitus with diabetic neuropathy, unspecified

Interventions

Intervention 1: Intervention group: The patients of the intervention group use chamomile oil in the base of sesame oil topically twice a day for 3 months. Intervention 2: Control group: Patients in th

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: People over 18 years old with diabetic neuropathy Being treated with routine medications to treat diabetes The patient has controlled diabetes. (In controlled diabetes, the patient's HbA1c is less than 7) Patients should be on gabapentin for diabetic neuropathy The neurothesiometer results should be greater than 15 and less than 25 Having at least reading and writing literacy

Exclusion criteria

Exclusion criteria: The patient does not agree to participate in the study Patients not receiving modern treatment for diabetes or abandoning treatment The patient use other topical, oral or injectable drugs effective on neuropathy The patient has skin allergy The patient have other diseases affecting the results (lumbar disc, sciatica, radiculopathy, peripheral vascular disease, MS, nerve damage diseases such as tarsal tunnel syndrome, etc.). Patients with foot or finger ulcers are excluded from the study due to the distortion of neurosimetry results Use other treatments such as physiotherapy, ultrasound therapy and laser therapy.

Design outcomes

Primary

MeasureTime frame
Sensitivity to vibration. Timepoint: Before the intervention, 2 and 3 months after the start. Method of measurement: Neurothesiometer.;Michigan questionnaire score. Timepoint: Before the intervention, 2 and 3 months after the start. Method of measurement: Questionnaire.;DN4 questionnaire score. Timepoint: Before the intervention, 2 and 3 months after the start. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Fasting Blood Sugar (FBS). Timepoint: Befor and After intervention. Method of measurement: Blood Test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Amiri

Shiraz University of Medical Sciences

dr.mohammad.amiri@gmail.com+98 71 3136 6885

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 5, 2026