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NCT02733991COMPLETEDanonymous

Study of MiniMed™ 640G Insulin Pump With SmartGuard™ in Prevention of Low Glucose Events in Adults With Type 1 Diabetes

Sponsor

Source record

Medtronic MiniMed, Inc.

Phase

Source record

Premarket (not classified under traditional clinical phases)

Modality

AI-normalized

medical device

Target

AI-normalized

Insulin delivery system with predictive low glucose management capabilities.

Indication / condition

AI-normalized

Type 1 Diabetes

Intervention

Source record

MiniMed™640G and Suspend before low, MiniMed™640G

Source & freshness

Source record

NCT ID

NCT02733991

Original source

ClinicalTrials.gov

Source last updated

Jan 21, 2020

Ingested at

Jun 18, 2026

Internal sync

Jun 18, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

Open original registry record
View original source fields

NCT ID

NCT02733991

Title

Study of MiniMed™ 640G Insulin Pump With SmartGuard™ in Prevention of Low Glucose Events in Adults With Type 1 Diabetes

Sponsor

Medtronic MiniMed, Inc.

Status

COMPLETED

Phase

Premarket (not classified under traditional clinical phases)

Condition raw

Type 1 Diabetes

Condition normalized

Type 1 Diabetes

Modality raw

medical device

Modality normalized

medical device

Target raw

Insulin delivery system with predictive low glucose management capabilities.

Target normalized

Insulin delivery system with predictive low glucose management capabilities.

Interventions

MiniMed™640G and Suspend before low, MiniMed™640G

Public preview

Source record

The MiniMed™ 640G insulin pump with SmartGuard™ technology represents a significant advancement in diabetes management, particularly for adults with Type 1 diabetes at high risk of hypoglycemia. The study's completion and positive outcomes suggest a strong market potential, particularly in regions with high diabetes prevalence. Competitive analysis indicates that Medtronic MiniMed, Inc. is positioned favorably against other insulin delivery systems, especially those lacking predictive features. The results may enhance Medtronic's market share and provide leverage in negotiations with payers and healthcare providers. Diligence should focus on regulatory pathways and reimbursement strategies, given the device's unapproved status in certain markets.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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