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Clinical Study on the Improvement of Diabetic Neuropathic Pain by Liraglutide
Lead sponsor
Asset
Liraglutide
Subcutaneous · GLP-1 agonist
Listed sites
0
Recruiting sites
—
Enrollment
60
estimated
Study population
Diabetic neuropathy, Type 2 diabetes
Key I/E criterion
—
Primary endpoint
•Numerical pain scale (NRS)
Identifiers
Registered as
Timeline
Milestones
Assets
Investigational agents
Study populations
Who this study enrolls
Eligibility
Who can enroll
Inclusion criteria
Age ≥ 18 and ≤ 80; The patients were diagnosed as type 2 diabetic neuropathic pain, and the score of pain digital scoring method was more than 3 points; 7-9% of glycosylated hemoglobin had poor blood glucose control.
Exclusion criteria
Non diabetic neuropathic pain; BMI < 20kg / m2; There are serious primary diseases such as cardiovascular, liver, kidney and hematopoietic system; In the past 1 month, there were acute complications such as diabetic ketoacidosis, lactic acidosis and hyperosmotic coma; Over the past five years, there have been alcoholics and / or psychoactive substances, drug abusers and addicts; Pregnant or lactating women; Unwillingness to cooperate or various factors affecting compliance; Psychopaths; Those who have participated in other clinical projects in the past 1 month.
Endpoints (3)
What's being measured
Protocol endpoints and posted registry outcome measures, grouped into outcome categories. Composite endpoints show their component event types. Standard codes (LOINC, SNOMED CT) are shown where available.
Other clinical outcomes
3 endpointsNumerical pain scale (NRS)
Time frame:3 months
descriptive, improvement
Neurological symptom score (NSS) / neurological deficit score (NDS)
Time frame:3 months
threshold achievement, improvement
Examination of nerve conduction function
Time frame:3 months
descriptive
Publications (10)
Bibliography
Records linked to this trial through ClinicalTrials.gov references, PubMed NCT search, and curated study seeds. 'Canonical' marks design/result papers; others are registry references or candidates.
Registry references + supporting bibliography
- Psychology & health2019 Jan (month)PMID30320508doi:10.1080/08870446.2018.1518526via CT.gov background
- Molecular neurobiology2018 Apr (month)PMID28456941doi:10.1007/s12035-017-0550-2via CT.gov background
- Journal of diabetes investigation2016 Apr (month)PMID27186361doi:10.1111/jdi.12446via CT.gov background
- Journal of diabetes investigation2016 Jan (month)PMID26813032doi:10.1111/jdi.12379via CT.gov background
- Arquivos brasileiros de endocrinologia e metabologia2014 Jun (month)PMID24936731doi:10.1590/0004-2730000002914via CT.gov background
- Diabetes research and clinical practice2010 Jun (month)PMID20359765doi:10.1016/j.diabres.2010.02.002via CT.gov background
Provenance
Sources
Trial facts come from public ClinicalTrials.gov records. Endpoint categories are Delfa's classification of those records, not a ClinicalTrials.gov field. All figures reflect the July 1, 2026 snapshot.