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Comparison of feeding tubes placed through the abdomen versus the nose for patients undergoing surgery for stomach cancer.

A SINGLE CENTRE RANDOMISED CONTROLLED TRIAL COMPARING FEEDING JEJUNOSTOMY VERSUS NASOJEJUNAL TUBE FEEDING IN PATIENTS UNDERGOING SURGERY FOR RESECTABLE GASTRIC CANCER - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/05/110241
Enrollment
250
Registered
2026-05-08
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Health Condition 1: C168- Malignant neoplasm of overlappingsites of stomach Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: Nasojejunal Tube Feeding: A 14 French nasojejunal tube will be inserted intraoperatively into the efferent jejunal limb under direct vision during reconstruction after gastrectomy. The

Sponsors

Basavatarakam Indo American Cancer Hospital and Research Institute
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age 18 years till 75 years ECOG performance status 0 to 2 Histologically confirmed resectable gastric cancer Planned curative gastrectomy with D2 lymphadenectomy Able to provide informed consent Both open and laparoscopic cases

Exclusion criteria

Exclusion criteria: Unresectable or metastatic disease detected preoperatively or intraoperatively. Previous upper gastrointestinal surgery or existing feeding access. Palliative intent surgery Severe comorbid illness precluding major surgery. Patients unwilling to participate or refusing consent.

Design outcomes

Primary

MeasureTime frame
To compare postoperative tolerance and complications related to enteral feeding between feeding jejunostomy (FJ) and nasojejunal (NJ) tube feeding after curative surgery for resectable gastric cancer.Timepoint: within 7 postoperative days

Secondary

MeasureTime frame
To compare time to achieve full enteral feeding in both groupsTimepoint: within 30 days postoperatively;To compare postoperative complications, including Clavien-Dindo grade complicationsTimepoint: 30 days postoperatively;To compare serum albumin levels preoperativelyTimepoint: 2 and 4 weeks postoperatively;To compare body weight changes, measured preoperativelyTimepoint: 1, 2, 3, and 4 weeks;To compare length of hospital stay and ICU stayTimepoint: within 30 days postoperatively

Countries

India

Contacts

Public ContactSyed Nusrath

Basavatarakam Indo American Cancer Hospital and Research Institute

mamidimanishareddy@gmail.com9494262898

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026