NCT06039306

Perioperative Immunonutrition Under Enhanced Recovery After Surgery

Perioperative Immunonutrition Among Gynecological Cancer Patients Under Enhanced Recovery After Surgery

• Status: Recruiting
• Phase: N/A
• Study type: Interventional
• Enrollment: 106 (estimated)
• Sponsor: Universiti Putra Malaysia · Academic / Other
• Sex: Female
• Age: 18 Years – 80 Years
• Healthy volunteers: Not accepted

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.

Detailed description

The clinical trial aims to determine the effectiveness of perioperative IMN intervention on postoperative outcomes among GC patients under Enhanced Recovery after Surgery (ERAS) setting. Patients will prescribed with immunonutrition supplement before and after surgery.

Conditions

• Gynecological Cancer
• Elective Surgery

Interventions

Type	Name	Description
DIETARY_SUPPLEMENT	Immunonutrition oral nutrition supplementation	Participant will prescribed with 2 servings of immunonutrition supplement 5 days before surgery and 7 days after surgery

Timeline

• Start date: 2024-09-01
• Primary completion: 2025-10-30
• Completion: 2025-10-30
• First posted: 2023-09-15
• Last updated: 2025-08-19

Locations

1 site across 1 country: Malaysia