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Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.

Contact Information:

Victoria Corner 01962 824127
victoria.corner@hhft.nhs.uk


Study Location:

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Be Part of Research - Trial Details - Post Splenectomy Infections After Surgery for Peritoneal Malignancies (OPSI)

Post Splenectomy Infections After Surgery for Peritoneal Malignancies (OPSI)

Recruiting

Open to: ALL

Age: 18.0 - 79.0

Medical Conditions

Infections
Communicable Diseases


This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


The spleen is involved in maintaining immunity and plays an important role in the elimination of encapsulated bacteria and parasites. Patients who undergo splenectomy in conjunction with complete CRS for peritoneal malignancy are at risk of overwhelming post-splenectomy infections post-operatively. These patients are therefore administered vaccinations to lower the risk of infections but as they do not completely eliminate the risk, patients are also prescribed prophylactic antibiotics without clear evidence that they are useful in preventing OPSI. The use of prophylactic antibiotics is not without risk with potential short and long-term risks including resistance, interaction with other medication, clostridium difficile infections, fungal infections, other changes to the microbiome and cost. This study will investigate the incidence of OPSI post splenectomy and assess compliance with prophylactic antibiotics. This is an observational study where consented patients will be telephoned at fixed time points which are 1,6,12 weekly and 6 monthly for a period of five years post-operatively. As part of routine care patients will be telephoned by the clinical nurse specialist at weeks 1,6 and 12. In addition to this the research nurse will telephone the patient 6 monthly for a period of 5 years and complete a questionnaire. The research nurse will complete the questionnaire during each telephone call and this should not take more than 20 minutes. At the start of the telephone call, consent will be confirmed each time and the research nurse will check that the patient is still happy to participate before going ahead.

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

Mar 2021 Feb 2026

OBSERVATIONAL

Intervention Type : OTHER
Intervention Description : Questionnaire administered by telephone




You can take part if:



You may not be able to take part if:


This is in the inclusion criteria above


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • The Peritoneal Malignancy Institute, Hampshire Hospitals NHS Foundation Trust
    Basingstoke
    Hampshire
    Rg24 9NN


The study is sponsored by Hampshire Hospitals NHS Foundation Trust




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Read full details for Trial ID: NCT05718726
Last updated 25 November 2024

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