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UnknownPhase NA

Clinical Study on the Improvement of Diabetic Neuropathic Pain by Liraglutide

Lead sponsor

Fudan University

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

NCT IDNCT04137328
Org study ID358106

Timeline

Milestones

Study first posted2019-10-24actual
Last update posted2019-10-25actual
Study start2019-11-30estimated
Primary completion2022-11-30estimated
Study completion2022-11-30estimated

Assets

Investigational agents

Study populations

Who this study enrolls

Diabetic neuropathyType 2 diabetes

Eligibility

Who can enroll

Minimum age18 Years
Maximum age80 Years
SexAll
Healthy volunteersNot accepted

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 endpoints
Primary/protocol endpoint

Numerical pain scale (NRS)

Time frame:3 months

descriptive, improvement

Secondary/protocol endpoint

Neurological symptom score (NSS) / neurological deficit score (NDS)

Time frame:3 months

threshold achievement, improvement

Secondary/protocol endpoint

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

Provenance

Sources

Trial identity, design, statusClinicalTrials.gov API v2
Snapshot dateJuly 1, 2026
Endpoint classificationDelfa endpoint taxonomy v2 (May 13, 2026)
Results tableno registry results posted yet

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.