Actively Recruiting
Impact of PErioperative Nutrition Intervention on Bioimpedance Phase Angle (IPENIPA) In Breast Cancer Patients
Led by University of Malaya · Updated on 2025-03-26
114
Participants Needed
1
Research Sites
94 weeks
Total Duration
On this page
Sponsors
U
University of Malaya
Lead Sponsor
B
B-Crobes Laboratory (M) Sdn Bhd
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this clinical trial is to measure the mean difference of phase angle after nutritional intervention in breast cancer patients. The main question it aims to answer is: 1\. Can perioperative nutrition interventions improve phase angle in relation to other bioimpedance parameters, handgrip strength and surgical outcomes in breast cancer population? Researchers will compare oral nutritional supplement to a placebo to see if oral nutritional supplement can improve phase angle. Participants will: 1. Be randomized into either arm 2. Take oral nutritional supplement or placebo according to the result of randomization for 7 days preoperatively and 30 days postoperatively 3. Have their measurements (weight, height, phase angle, handgrip strength) done at least 7 days preoperative, 1 day preoperative and 30 days postoperative
CONDITIONS
Official Title
Impact of PErioperative Nutrition Intervention on Bioimpedance Phase Angle (IPENIPA) In Breast Cancer Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female
- Histopathologically confirmed operable breast cancer
- Aged 18 years and above
- Consented and scheduled for mastectomy
You will not qualify if you...
- On enteral supplementation prior to the study
- Lactose intolerance
- Pregnant or lactating
- Previous history of gastrectomy or small bowel resection surgery
- Advanced breast cancer staging
- Presence of pacemaker
- Decompensated liver disease
- End stage renal failure
- Uncontrolled diabetes
- On steroid therapy or complementary traditional medications
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Trial Site Locations
Total: 1 location
1
Universiti Malaya Medical Centre
Petaling Jaya, Kuala Lumpur, Malaysia, 50603
Actively Recruiting
Research Team
W
Wai Yin Soo, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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