RecruitingNot ApplicableNCT06039306

Perioperative Immunonutrition Under Enhanced Recovery After Surgery

Perioperative Immunonutrition Among Gynecological Cancer Patients Under Enhanced Recovery After Surgery


Sponsor

Universiti Putra Malaysia

Enrollment

106 participants

Start Date

Sep 1, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The goal of this clinical trial is to compare the effect of perioperative immunonutrition supplement in gynecologic cancer patients. The main questions it aims to answer are: * is there any difference in the nutritional outcomes and functional outcomes between intervention and conventional groups? * is there any difference in the post-surgical outcomes between intervention and conventional groups? Participants (intervention) will be provided the immunonutrition supplement before and after operation. Researchers will compare intervention group with conventional group to see if there is any difference in postoperative outcomes.


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 80 Years

Inclusion Criteria2

  • Those who diagnosed with GC
  • Candidates for elective operation treatments

Exclusion Criteria4

  • Those are involved gastrointestinal tract (complication)
  • Those are diagnosed with GC (metastasis)
  • Allergy to milk/soy/whey protein
  • Participate in other intervention study

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Interventions

DIETARY_SUPPLEMENTImmunonutrition oral nutrition supplementation

Participant will prescribed with 2 servings of immunonutrition supplement 5 days before surgery and 7 days after surgery


Locations(1)

Institut Kanser Negara

Putrajaya, Putrajaya, Malaysia

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NCT06039306


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