The Therapeutic Effects of Ceylon Cinnamon Supplementation and a Self-Efficacy Educational Program on Glycemic Control, Lipid Profiles, and Pain in Type 2 Diabetes Mellitus With Painful Diabetic Peripheral Neuropathy
- NCT ID
- NCT07757399
- Registry status
- Not yet recruiting
- Study type
- Not specified in the registry data
- Phase
- Not applicable
- Sponsor
- Jerash Private University
Overview
ClinicalTrials.gov lists this study as Not yet recruiting.
Enrollment: 900 participants (Estimated).
What is being studied
No interventions are listed in the registry data.
Who may be eligible
- Ages
- Not specified in the registry data
- Sex
- Not specified in the registry data
- Healthy volunteers accepted
- No
ClinicalTrials.gov lists the following eligibility criteria.
Inclusion Criteria:
* Diagnosed with Type 2 Diabetes Mellitus (T2DM) for at least 6 months.
* Confirmed diagnosis of painful diabetic peripheral neuropathy (PDPN).
* Age between 18 and 65 years.
* Able to provide written informed consent and willing to comply with the study protocol, supplement intake, and educational sessions.
Exclusion Criteria:
* Type 1 diabetes mellitus or gestational diabetes.
* Severe renal or hepatic impairment.
* Known allergy, hypersensitivity, or contraindication to cinnamon or related botanical products.
* Pregnancy or lactation.
* Concurrent participation in another clinical trial or severe psychiatric/cognitive disorders that hinder study participation.
Study locations
No study locations are listed in the registry data.
Study details
- Start date
- August 1, 2026
- Primary completion date
- December 1, 2026
- First posted
- August 11, 2026
Source and update information
- Source
- ClinicalTrials.gov
- NCT ID
- NCT07757399
- Registry last updated
- August 11, 2026
- QualifiedStudies registry data refreshed
- September 21, 2026
View NCT07757399 on ClinicalTrials.gov
Trial information can change. Confirm current study details with the study team or the registry.
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