Efficacy of Dapagliflozin in Diabetes Associated Peripheral Neuropathy

NCT ID: NCT05162690

Last Updated: 2022-06-07

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2/PHASE3
• Total Enrollment: 40 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-05-01
• Study Completion Date: 2023-12-31

Brief Summary

Diabetic peripheral neuropathy(DPN) is a length dependent axonal neuropathy that affects at least 50% of patients with diabetes mellitus. DPN is often asymptomatic during the early stages of diabetes ,however, once symptoms and overt deficits have developed, it cannot be reversed. Early diagnosis of neuropathy is important because early diagnosis and timely intervention might prevent the development and progression of diabetic neuropathy.Though glycemic control has been shown to prevent the progression of diabetic microvascular complications including diabetic peripheral neuropathy in Type I DM, such strict glycemic control has not shown to improve diabetic peripheral neuropathy in Type 2 DM. There are only few animal studies conducted so far which have shown that the use of SGLT2 inhibitors prevents the progression of diabetic peripheral neuropathy.Thus the investigators postulate that the use of SGLT2 inhibitor in patients with Type 2 Diabetes Mellitus might be beneficial in the prevention of progression of diabetic peripheral neuropathy as well as reverse it.

Detailed Description

Diabetic peripheral neuropathy is a length dependent axonal neuropathy that affects at least 50% of patients with diabetes mellitus. It is characterized by sensory loss and pain that initially affects small unmyelinated C fibers which is followed by involvement of the large myelinated fibers as diabetes progresses. DPN is often asymptomatic during the early stages of diabetes ,however, once symptoms and overt deficits have developed, it cannot be reversed. Early diagnosis of neuropathy is thus important because early diagnosis and timely intervention might prevent the development and progression if diabetic neuropathy and might provide us with a means to identify patients at high risk for future complications of DPN which includes risk of foot ulcers and lower limb amputation.

Methods to quantify neuropathy include clinical scores based on symptoms and neurological tests, quantitative sensory testing, electrophysiological measurements, in the form of nerve conduction studies and intraepidermal nerve fiber density in skin biopsy specimens. The neurological examination involves an assessment, such as modified neuropathy disability score, a composite score that assesses touch, temperature and vibration perception and reflexes, which require expert clinical judgement, a strong element of subjectivity and hence poor reproducibility. Neurophysiology is objective and reproducible and is currently considered to be the most reliable measurements for confirming the diagnosis of diabetic neuropathy. However, these measures mainly assess large nerve fibers, making them less sensitive to early DPN,which is more likely to involve the small fibers to begin with.

Objective measures are thus required to accurately determine nerve pathology to detect early stages of DPN, which may be more susceptible to intervention than late-stage sequelae. Small fibers, which constitute 70-90% of peripheral nerve fiber, may be measured in skin biopsies by assessing intraepidermal nerve fiber density, which is considered to be the gold standard for the evaluation of small fibers damage. Indeed, the European Federation of the Neurological Societies and the Peripheral Nerve Society endorse intraepidermal nerve fiber quantification to confirm the clinical diagnosis of small fiber neuropathy with a strong (Level A)recommendation.

Recently, corneal confocal microscopy (CCM), a noninvasive modality for the study of the human cornea, has emerged as a promising technique for the detection of small nerve fiber alterations. CCM is a rapid non-invasive imaging technique for the quantitative assessment of small fiber damage. Several studies have shown that it has good diagnostic utility for sub-clinical DPN, predicts incident DPN and correlates with other measures of neuropathy . Furthermore, automated quantification of corneal nerve parameters allows rapid, unbiased and objective assessment of small fiber damage with comparable diagnostic capability to intraepithelial nerve fiber density (IENFD). Recent data also suggest that CCM shows good reproducibility and could be useful to document nerve regeneration after treatment and simultaneous pancreas and kidney transplantation.

There is currently no Food and Drug Administration (FDA) approved therapy to prevent or reverse human DPN. The current management approach focuses on reasonable glycemic control, and management of associated pain. Sodium-glucose cotransporter 2 (SGLT2) inhibitors as oral hypoglycemic agents have been approved for treating type 2 diabetes mellitus (T2DM). The insulin-independent action mechanism and extra-metabolic benefits of these agents have encouraged ongoing preclinical and clinical trials for evaluating the efficacy and safety of SGLT2 inhibitors. In addition to glucose-lowering effects without hypoglycemia, SGLT2 inhibitors retard the development and progression of diabetic complications. However, it is uncertain whether this effect of SGLT2 inhibitors is due to their glucose-lowering effect or not. In addition, unlike diabetic nephropathy, the effects of SGLT2 inhibitors on diabetic peripheral neuropathy are unexplored.

To date, only three studies regarding the effects of SGLT2 inhibitors for DPN in T2DM animal models are reported. Investigators evaluated neuronal effects in terms of simple functional parameters, such as motor nerve conduction velocity and tail flick test. Results of these studies verified the beneficial effects of SGLT2 inhibitors for DPN, and these effects were considered to indirect effects of the improvement of hyperglycemia.

Since no human studies have yet been conducted using SGLT2 inhibitors in the prevention and progression of diabetic neuropathy, hence, investigators plan to conduct a randomized controlled trial evaluating the efficacy of dapagliflozin in diabetic peripheral neuropathy

Conditions

Diabetic Peripheral Neuropathy

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

The Drug Arm

Dapagliflozin 10 milligram Once a day

1 year

Group Type: ACTIVE_COMPARATOR

Dapagliflozin 10 milligram

Intervention Type: DRUG

10mg per day of Dapagliflozin will be given to the patients

The Placebo Arm

Metformin 1gram Per Oral Twice a day Glimepiride 2 milligram oral twice a day Dipeptidyl peptidase 4 inhibitors (DPP4 inhibitors)

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: OTHER

Metformin DPP4 inhibitors

Interventions

Dapagliflozin 10 milligram

10mg per day of Dapagliflozin will be given to the patients

Intervention Type: DRUG

Placebo

Metformin DPP4 inhibitors

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

-

Type 2 Diabetes Mellitus < 5 years duration

Age >18yrs

Presence of neuropathy at baseline (accessed by Michigan Neuropathy Screening Instrument score >7 )

estimated Glomerular Filtration rate (eGFR) > 45ml/min/m2

HBA1c < 9

Exclusion Criteria

Untreated Hypothyroidism

Patients currently on SGLT2 inhibitors History of Leprosy

Patients with history of and current foot ulcers

Presence of Peripheral Vascular disease(ABI <0.9)

B12(<200 pg/ml)/ Folate (<4.6 ng/ml)

History of alcohol abuse (>2 standard drink per day for males and >1 standard drink for females)

Factors affecting corneal nerves( severe dry eyes, severe corneal dystrophies, ocular trauma or surgery in the preceding 6 months)

Negative consent

-

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Post Graduate Institute of Medical Education and Research, Chandigarh

OTHER

Sponsor Role: lead

Responsible Party

Ashu Rastogi

Associate Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Ashu Rastogi, DM

Role: PRINCIPAL_INVESTIGATOR

PGIMER, India

Locations

Department of Endocrinology, PGIMER

Chandigarh, , India

Site Status: RECRUITING

Countries

India

Central Contacts

Ashu Rastogi, MD, DM

Role: CONTACT

rastogi.ashu@pgi.ac.in

9781001046

Facility Contacts

Ashu Rastogi, DM

Role: primary

rastogi.ashu@pgimer.ac.in

9781001046

References

Adhikari U, Gad H, Chatterjee D, Malhotra C, Bhadada SK, Malik RA, Rastogi A. Dapagliflozin for Small Nerve Fibre Regeneration in Diabetic Peripheral Neuropathy: A Randomised Controlled Study (DINE). J Peripher Nerv Syst. 2025 Mar;30(1):e70011. doi: 10.1111/jns.70011.

Reference Type: DERIVED

PMID: 40044634 (View on PubMed)

Other Identifiers

PGIMER1

Identifier Type: -

Identifier Source: org_study_id