PENTAC: Penetration of Cefazolin Into Hepatic Cysts

Sponsor
Radboud University Medical Center (Other)
Overall Status
Completed
CT.gov ID
NCT02368015
Collaborator
(none)
8
1
1
13
0.6

Study Details

Study Description

Brief Summary

Hepatic cysts are fluid-filled cavities located in the liver parenchyma. They are usually asymptomatic, but can cause mass-related symptoms as abdominal pain, dyspnea and nausea. Aspiration sclerotherapy is indicated in patients with a dominant hepatic cyst to alleviate symptoms by draining the hepatic cyst to reduce cyst diameter. Spontaneous cyst infection, or following aspiration sclerotherapy, presents a severe complication of hepatic cystic disease requiring frequent hospitalization, long-term antibiotic treatment, and in some invasive therapies. Evidence that antibiotics are able to reach adequate intracystic concentration is however lacking. To prevent procedure-related cyst infection in patients receiving aspiration sclerotherapy, cefazolin prophylaxis is given as standard of care. In this study we want to assess the hepatic cyst penetration capacity of cefazolin by comparing serum and cyst fluid concentrations of cefazolin. We hypothesize that cefazolin is able to penetrate hepatic cysts, with treatment naïve cyst allowing a better penetration, reducing the risk of developing cyst infection following aspiration sclerotherapy.

Condition or Disease Intervention/Treatment Phase
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
8 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Official Title:
An Explorative Study Determining the Hepatic Cyst Penetration of Cefazolin and Factors Affecting Penetration.
Study Start Date :
Dec 1, 2014
Actual Primary Completion Date :
Dec 1, 2015
Actual Study Completion Date :
Jan 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Other: Patients with a large hepatic cyst

During this study all subjects undergo aspiration sclerotherapy and receive antibiotic prophylaxis with a single dose of cefazolin (intravenous infusion 1000mg) following standard care. In order to secure patient safety and allow accurate measurement of cefazolin concentrations, an additional peripheral intravenous cannula (IVC) will be placed to allow blood withdrawal at three timepoints.

Other: Peripheral intravenous cannula (IVC)
Blood samples will be withdrawn prior, during and after the procedure using an additional peripheral intravenous cannula (IVC).

Drug: cefazolin

Outcome Measures

Primary Outcome Measures

  1. Hepatic cyst penetration of cefazolin defined as the ratio (%) of cyst aspirate concentration (µg/ml) to serum concentration (µg/ml) of cefazolin. [Intraoperative]

Secondary Outcome Measures

  1. Segmental location (I-VIII) of hepatic cyst [Baseline]

  2. Volume (mL) of hepatic cyst [Baseline]

  3. Blood parameter: total protein (g/l) [Intraoperative]

  4. Blood parameter: albumin (g/l) [Intraoperative]

  5. Blood parameter: urea (mmol/l) [Intraoperative]

  6. Blood parameter: white blood cell count (*10^9/l) [Intraoperative]

  7. Blood parameter: white blood differentiation (%) [Intraoperative]

  8. Blood parameter: CRP (mg/l) [Intraoperative]

  9. Blood parameter: direct bilirubin (µmol/L) [Intraoperative]

  10. Blood parameter: total bilirubin (µmol/L) [Intraoperative]

  11. Blood parameter: CA 19.9 (E/ml) [Intraoperative]

  12. Blood parameter: creatinine (µmol/L) [Intraoperative]

  13. Cyst fluid parameter: total protein (g/l) [Intraoperative]

  14. Cyst fluid parameter: albumin (g/l) [Intraoperative]

  15. Cyst fluid parameter: urea (mmol/l) [Intraoperative]

  16. Cyst fluid parameter: white blood cell count (*10^9/l) [Intraoperative]

  17. Cyst fluid parameter: white blood cell differentiation (%) [Intraoperative]

  18. Cyst fluid parameter: CRP (mg/l) [Intraoperative]

  19. Cyst fluid parameter: direct bilirubin (µmol/L) [Intraoperative]

  20. Cyst fluid parameter: total bilirubin (µmol/L) [Intraoperative]

  21. Cyst fluid parameter: CA 19.9 (E/ml) [Intraoperative]

  22. Cyst fluid parameter: sodium (mmol/l) [Intraoperative]

  23. Cyst fluid parameter: pH [Intraoperative]

  24. Number of patients that develop clinical signs indicating aspiration sclerotherapy-induced cyst infection [Until four weeks after aspiration sclerotherapy]

  25. Number of participants with adverse events [until four weeks after aspiration sclerotherapy]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age ≥18 years

  • Indication for aspiration and sclerotherapy

  • Providing informed consent

Exclusion Criteria:
  • Presence of an arteriovenous fistula, history of mastectomy or lymph node dissection at both extremities

  • Signs of phlebitis, defined as localized skin redness and swelling, at both extremities

  • History of cephalosporin and/or penicillin allergy consisting of IgE-mediated reactions as anaphylaxis, angioedema, urticaria.

  • Any current or prior medical condition that may interfere with the conduct of the study or the evaluation of its results in the opinion of the investigator.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Radboud University Nijmegen Medical Center; Department of Gastroenterology & Hepatology Nijmegen Gelderland Netherlands 6500 HB

Sponsors and Collaborators

  • Radboud University Medical Center

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Radboud University Medical Center
ClinicalTrials.gov Identifier:
NCT02368015
Other Study ID Numbers:
  • NL49426.091.14
First Posted:
Feb 20, 2015
Last Update Posted:
Feb 3, 2016
Last Verified:
Feb 1, 2016
Keywords provided by Radboud University Medical Center
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 3, 2016