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Combined Oral and Parenteral Nutritional Therapy After Gastrectomy for Gastric Cancer

Bridging the Postoperative Nutritional Gap After Gastrectomy for Gastric Cancer: A Prospective Randomized Trial of Combined Oral and Parenteral Nutritional Therapy

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07604857
Acronym
BRIDGE-GC
Enrollment
55
Registered
2026-05-22
Start date
2020-10-01
Completion date
2024-05-31
Last updated
2026-05-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gastric Cancer (GC), Malnutitrion

Keywords

Gastrectomy, Parenteral Nutrition, Oral Nutritional Supplement, Postoperative Recovery, Nutritional Support, Body Weight Loss, Randomized Trial

Brief summary

Patients undergoing gastrectomy for gastric cancer frequently experience insufficient oral intake during the postoperative recovery period because of reduced gastric capacity, early satiety, and gastrointestinal symptoms. Although oral nutritional supplements (ONS) are commonly recommended, adherence is often poor, resulting in a postoperative nutritional gap. This prospective randomized clinical trial was designed to evaluate the impact of combined oral and parenteral nutritional therapy on nutritional status and recovery after gastrectomy for gastric cancer. Patients were randomized to either a combined nutritional therapy group receiving oral nutritional supplementation plus parenteral nutrition or a control group receiving standard postoperative care. The primary endpoint was postoperative body weight change at 4 weeks after surgery. Secondary endpoints included body composition, nutritional intake, inflammatory and immune markers, laboratory parameters, and quality of life outcomes.

Detailed description

Postoperative nutritional deterioration remains a major clinical challenge after gastrectomy for gastric cancer. Reduced gastric capacity and postoperative gastrointestinal symptoms frequently result in inadequate oral intake during the early recovery period. Although oral nutritional supplements are widely recommended, adherence is often poor, potentially leading to insufficient caloric intake and postoperative nutritional deficits. This prospective randomized clinical trial evaluates whether combined oral and parenteral nutritional therapy can improve postoperative nutritional status and recovery compared with standard postoperative care. Patients undergoing curative gastrectomy for gastric cancer are randomized to receive either combined oral nutritional supplementation plus parenteral nutrition or standard postoperative nutritional management. Nutritional outcomes including body weight, body mass index, body composition, inflammatory markers, laboratory nutritional parameters, caloric intake, oral nutritional supplement adherence, and quality of life are assessed during the postoperative recovery period. This study aims to clarify the clinical significance of supplemental parenteral nutrition in bridging the postoperative nutritional gap after gastrectomy.

Interventions

Patients received oral nutritional supplementation using Encover® three times daily during the postoperative recovery period after gastrectomy for gastric cancer.

OTHERParenteral Nutrition

Supplemental parenteral nutrition was administered during hospitalization and after discharge to support postoperative nutritional requirements.

OTHERStandard Postoperative Nutritional Care

Standard postoperative nutritional management according to institutional clinical pathways, including routine postoperative diet advancement and conventional nutritional support.

Sponsors

Kyo Young Song
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Masking description

Because of the nature of the nutritional intervention, participants and investigators were not blinded to treatment allocation.

Intervention model description

Participants were randomized in a 1:1 ratio to receive either combined oral and parenteral nutritional therapy or standard postoperative nutritional care after gastrectomy for gastric cancer.

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Age 20 to 80 years * Histologically confirmed gastric cancer * Scheduled for curative total or subtotal gastrectomy * Ability to tolerate oral intake * Residence within areas covered by home care services * Written informed consent

Exclusion criteria

* Body mass index (BMI) ≥30 kg/m² or \<18.5 kg/m² * Uncontrolled diabetes mellitus * Severe hepatic or renal dysfunction * Active malignancy other than gastric cancer * Previous chemotherapy or radiotherapy * Allergy to oral nutritional supplement products

Design outcomes

Primary

MeasureTime frameDescription
Postoperative Body Weight Change4 weeks after surgeryDifference between preoperative body weight and body weight measured at 4 weeks after gastrectomy for gastric cancer.

Secondary

MeasureTime frame
Body Mass Index Change4 weeks after surgery

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 23, 2026