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NCT01605006COMPLETEDanonymous

HDE Post-Approval Study (PAS) of NeuRx DPS for ALS

Sponsor

Source record

Synapse Biomedical

Phase

Source record

Post-Approval Study (HDE PAS)

Modality

AI-normalized

medical device

Target

AI-normalized

Diaphragm muscle stimulation via phrenic nerve activation.

Indication / condition

AI-normalized

Amyotrophic Lateral Sclerosis (ALS)

Intervention

Source record

NeuRx Diaphragm Pacing System (DPS)

Source & freshness

Source record

NCT ID

NCT01605006

Original source

ClinicalTrials.gov

Source last updated

Mar 27, 2020

Ingested at

Jun 12, 2026

Internal sync

Jun 12, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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View original source fields

NCT ID

NCT01605006

Title

HDE Post-Approval Study (PAS) of NeuRx DPS for ALS

Sponsor

Synapse Biomedical

Status

COMPLETED

Phase

Post-Approval Study (HDE PAS)

Condition raw

Amyotrophic Lateral Sclerosis (ALS)

Condition normalized

Amyotrophic Lateral Sclerosis (ALS)

Modality raw

medical device

Modality normalized

medical device

Target raw

Diaphragm muscle stimulation via phrenic nerve activation.

Target normalized

Diaphragm muscle stimulation via phrenic nerve activation.

Interventions

NeuRx Diaphragm Pacing System (DPS)

Public preview

Source record

The NeuRx Diaphragm Pacing System (DPS) is positioned as a therapeutic intervention for patients with Amyotrophic Lateral Sclerosis (ALS) experiencing chronic hypoventilation. With a target enrollment of 60 participants, the study aims to assess the safety and probable benefits of the device over a two-year follow-up period. Given the increasing prevalence of ALS and the limited treatment options available, the NeuRx DPS addresses a significant unmet medical need in respiratory management for ALS patients. The competitive landscape includes traditional mechanical ventilation and other emerging therapies, but the NeuRx DPS offers a unique, less invasive alternative that could enhance patient quality of life. The successful demonstration of safety and efficacy could facilitate broader adoption and potential reimbursement pathways, enhancing market penetration. Diligence considerations should focus on regulatory compliance, post-market surveillance, and the evolving landscape of ALS treatment options.

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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