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Preoperative Immunonutrition in Patients With Bone and Soft Tissue Sarcomas

Sponsor: St. Anne's University Hospital Brno, Czech Republic · NCT07609329 on ClinicalTrials.gov ↗

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Conditions studied

Bone SarcomaSoft Tissue SarcomaSarcopeniaMalnutritionPostoperative Complications

What it tests

  • Forticare Advanced oral nutritional supplementdietary_supplement

Where it's running1 site

1 international site

  • First Department of Orthopaedic Surgery, St. Anne's University Hospital and Faculty of Medicine, Masaryk University, Brno, Czechia

    Brno, Czechia 60200

    Recruiting now
See the official eligibility language

Shown exactly as written on ClinicalTrials.gov. Your oncologist is the right person to judge whether it fits your situation.

Inclusion Criteria:

* Participants must meet all of the following criteria:
* Adult patients aged 18 years or older.
* Histologically confirmed bone sarcoma or soft tissue sarcoma.
* Localized or oligometastatic disease.
* Indicated for planned orthopedic tumor resection.
* Preoperative interval allowing administration of the nutritional intervention for at least 7 days, with 14 days preferred when clinically feasible.
* Ability to receive oral nutritional supplementation.
* Signed informed consent for participation in the study.

Exclusion Criteria:

* Participants will be excluded if any of the following criteria are present:
* Indication for urgent surgery.
* Disseminated disease with more than five metastases.
* Ongoing parenteral nutrition before study enrollment.
* Inability to receive oral intake.
* Severe hepatic failure.
* Severe renal failure.

Updated 2026-05-27 on ClinicalTrials.gov. Always confirm current details with the study team or your oncologist.