Clinical Trials Directory

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UnknownNCT03266042

Registry Protocol- Melphalan Percutaneous Hepatic Perfusion for the Treatment of Unresectable Hepatic Malignancy

Collection of Safety, Efficacy and Resource Utilization Information in Patients Who Have Received Melphalan PHP With the Delcath Hepatic Delivery System for the Treatment of Unresectable Hepatic Malignancy

Status
Unknown
Phase
Study type
Observational
Enrollment
200 (estimated)
Sponsor
Delcath Systems Inc. · Industry
Sex
All
Age
Healthy volunteers
Not accepted

Summary

Collection of Safety, Efficacy and Resource Utilization Information in Patients Who Have Received Melphalan PHP with the Delcath Hepatic Delivery System for the Treatment of Unresectable Hepatic Malignancy

Detailed description

Post Marketing study: The CHEMOSAT kit containing Gen 2 filters has been used to treat patients since April 2012. This registry study is designed to collect safety, resource utilization and treatment outcomes in patients who receive this treatment with CHEMOSAT by healthcare professionals. The safety and efficacy data from patients treated with CHEMOSAT is important in updating the safety profile and for collection of treatment information. The resource utilization information is essential in planning treatment strategy for patients. This registry does not follow any pre-determined protocol with respect to diagnosis, treatment or follow-up of the patient. The data collected will be gathered exclusively from current medical practice at participating institutions. Delcath holds a list of authorized customer hospitals to whom it supplies the CHEMOSAT System. To date these hospitals have treated over 300 patients with cancers of the liver. The decision to treat with CHEMOSAT is clearly separated from the decision to collect data in the registry. No specific procedures or tests are required in this protocol.

Conditions

Timeline

Start date
2016-01-14
Primary completion
2020-01-01
Completion
2020-02-01
First posted
2017-08-29
Last updated
2018-09-11

Locations

2 sites across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT03266042. Inclusion in this directory is not an endorsement.