EMPATHY: Evaluation of 'Melody' Paracentesis Device for Ascites Therapy
Study Details
Study Description
Brief Summary
Ascites is the accumulation of fluid inside the abdomen. This can happen when the liver fails due to a substantial amount of scarring (cirrhosis). Patients (pts) must have this fluid drained and as cirrhosis progresses, patients will require drainage of ascites repeatedly on a regular basis, leading to frequent hospitals visits and increased complications.
The current drainage device is slow and doesn't always drain completely so pts have to return repeatedly to keep symptoms under control.
A new device (called Melody) has been developed and specifically designed for the purpose of draining ascites fluid, which the Investigators expect to drain faster and completely.
This study will compare the volume of ascites drained using the new 'Melody' catheter device with that used in standard NHS practice. If the melody catheter device is confirmed as superior to the current device this would improve patient experience (less frequent visits to hospital and increased length of time between visits).
With fewer procedures performed per patient, the pressure on the NHS would be greatly reduced in terms of time and costs.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
Large volume paracentesis has been established as a treatment for symptomatic ascites and is performed regularly in secondary care hospitals widely across the UK.
Lack of a device specifically designed to perform paracentesis means that flow of ascites fluid through the catheter is not optimal leading to incomplete drainage and hence, frequent repeated paracentesis as well as a number of complications.
A new 'Melody' catheter device has been designed and developed in collaboration with Mediplus Ltd and NIHR Enteric Bowel function Healthcare Technology Co-operative; specifically designed to improve the performance characteristics of paracentesis procedure.
(The 'Melody ascites drainage catheter' including 'sterile ascetic drainage sets' is CE marked for clinical use). In addition, investigators would also like to confirm whether the addition of a pump will improve drainage with this device further.
The Investigators propose to carry out a feasibility study, 'EMPATHY', with an aim to compare the performance characteristics of 'Melody' catheter device (with and without addition of 'Andromeda' pump) with the current device. 112 patients with ascites requiring therapeutic paracentesis will be randomised to undergo the procedure using one of the two devices. The volume of ascites drained per session will be compared along with ease of insertion and removal as well as patient experience including all adverse events up to 7 days following the procedure. The outcomes of this feasibility study will inform further refinement of the 'Melody' catheter device as well as a future large multi-centre randomised controlled trial evaluating the cost-effectiveness of the new 'Melody' catheter device in therapeutic paracentesis
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Active Comparator: Standard Device Standard device |
Device: standard device
paracentesis using standard
|
| Experimental: Melody Device Melody device without Pump |
Device: Melody Device
paracentesis using Melody Device
Other Names:
|
| Experimental: Melody Device with pump Melody Catheter device with Andromeda Pump |
Device: Melody Device with Pump
paracentesis using Melody Device with Pump
Other Names:
|
Outcome Measures
Primary Outcome Measures
- Amount of ascites fluid drained (litres) [Up to 6 hours]
Amount of ascites fluid drained in one session (litres)
Secondary Outcome Measures
- Adverse Events [Up to 7 days]
As reported by patients using a visual analogue scale
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Ascites due to cirrhosis of the liver.
-
Aged 18-80 years.
-
Ability to give written consent.
Exclusion Criteria:
-
Known untreated spontaneous bacterial peritonitis.
-
Disseminated intravascular coagulation at the time of consenting.
-
Pregnancy.
-
Patients who have had more than six ascitic drainage procedures.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Queen Day Case Unit Nottingham University Hospitals NHS Trust | Nottingham | United Kingdom | NG7 2UH |
Sponsors and Collaborators
- University of Nottingham
- Mediplus Ltd UK
- Enteric healthcare technology Co-operative
Investigators
- Principal Investigator: Guruprasad Aithal, NIHR Nottingham Biomedical Research Centre, Nottingham University Hospitals NHS Trust & University of Nottingham
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 14083