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NCT Number: NCT05561907

Enteral Anastomosis for the Treatment of Gastric Outlet Obstruction: A Randomized Controlled Study Comparing Endoscopic Versus Surgical Gastrojejunostomy

Gastric outlet obstruction (GOO) occurs commonly in malignancies involving the periampullary region (cancers originating in the head of the pancreas, duodenum, bile duct, or ampulla) or the distal stomach. GOO not only causes debilitating symptoms such as nausea, vomiting, inability to tolerate oral intake, and prevents adequate nutritional intake. Therefore, providing therapy for GOO is imperative to improve the quality of life, and nutritional status of these patients, as well as allow them to continue receiving their cancer treatment

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Robert Wood Johnson University Hospital, New Brunswick, New Jersey, United States

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About this study

After potential subjects are screened from the physicians' schedules, they will be assessed for further inclusion criteria. They will be presented with the informed consent form for their review. Once they have been given the opportunity to review and ask questions, they will sign the consent form and from this point will be considered enrolled into the study.

After signing the informed consent, subjects will be randomized to one of the two cohorts in a 1:1 manner.

On the day of their assigned procedures, subjects will be asked several quality of life questionnaires to obtain a baseline status.

Data will be collected during and immediately following the procedure to assess for any possible adverse events.

Follow-up data will be completed at the following timepoints: 1-day, 2-day, 3-day, 4-day, and 7-day, 30-day, 3-month, 6-month, and 1-year post-procedure.

QOL Scoring Systems GOOSS- Gastric Outlet Obstruction Symptom Score

  • 1 Inadequate or no oral intake
  • 2 Liquids/thickened liquids
  • 3 Semisolids/ low residue
  • 4 unmodified

GFS- Gut Function Score from Lowe et al 2002

  • 0 Profuse vomiting
  • 1 Nausea and occasional vomiting
  • 2 Nausea only
  • 3 Normal gut function

Pre-Procedure Variables to Record Demographic

  • Gender
  • Weight
  • BMI
  • Cancer Type

Clinical Parameters

  • GOOSS
  • Gut Function Score
  • Karnofsky Performance Scale

Procedural Parameters

  • EUS-GJ: presence of ascites, able to pass scope beyond obstruction, use of wire to stabilize position, Length of procedure, intraprocedural AEs, Stent size used, successful completion of procedure
  • Laparoscopic GJ: presence of ascites, length of procedure, intraprocedural AEs, conversion to open GJ, successful completion of procedure

Post-procedure Hospitalization Daily Function

  • GOOSS
  • Gut Function Score
  • Time to initiation of oral intake liquids
  • Time to initiation of oral intake solids
  • Time to discharge
  • Post procedural AEs

30 Day Outcomes

  • GOOSS
  • Gut Function Score
  • Karnofsky Performance Scale
  • Weight/BMI
  • Able to tolerate TB approved chemotherapeutic regimen

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Periampullary malignancy (pancreas, bile duct, ampulla, duodenum) extending to the distal duodenum (D3) or distal (antrum) gastric cancer
  • Symptoms of gastric outlet obstruction (at least 2 of 4 required):
  • post prandial vomiting,
  • abdominal pain,
  • inability to tolerate PO,
  • imaging consistent with GOO
  • Gastric Outlet Obstruction Scoring System (GOOSS) Score of 0 (no oral intake) or 1 (liquids only)
  • Age >18 years old
  • Life expectancy greater than 2 months or failed duodenal stenting
  • Surgical Candidate/Tolerate General Anesthesia
  • Unresectable or metastatic disease

Exclusion criteria

  • Age< 18 years old
  • Pregnancy
  • Intestinal obstruction distal to the Ligament of Treitz
  • Evidence of other luminal strictures of the GI tract
  • Previous gastric or periampullary surgery
  • Inability to complete quality of life surveys (QOLS)
  • Presence of abdominal ascites

Treatment and study plan

Surgical gastrojejunostomy (SGJ)

Procedure

Laparoscopic gastrojejunostomy

Endoscopic gastrojejunostomy (EGJ)

Procedure

Endoscopic ultrasound (EUS) guided gastrojejunostomy

Primary outcomes

  1. Time to initiation of solid oral intake without symptoms of GOO

    Time frame: 1 year

    Days to initiation of solid oral intake will be measured from randomization to first day of intake of soft solid foods, as indicated by a GOOSS score of 2

Secondary outcomes

  1. Safety of procedure

    Time frame: 1 year

    All adverse events (AEs) occurring after treatment will be graded according to ASGE lexicon. A subject will be considered to have had an adverse event if they had one or more adverse events, and they will be considered to have had a serious adverse event (SAE) if they had one or more serious adverse events

  2. Technical success of procedure

    Time frame: 1 year

    Technical success is defined as adequate deployment and positioning of the stent(s) for EGJ or technical possibility to create an anastomosis for SGJ.

  3. Clinical success of procedure

    Time frame: 1 year

    Clinical success is defined as improvement to a GOOSS score of 2 or 3 (oral intake of soft solid foods or resumption of full diet) without additional intervention.

  4. Time to discharge

    Time frame: 1 year

    Length of stay will be measured from randomization to discharge alive. All patients will be followed until discharge. Patients who die in hospital will be considered censored and time from randomization to death will be used.

  5. Change in BMI

    Time frame: 3 months

    BMI will be measured immediately prior to the procedure, and at one month and three months after the procedure.

  6. Change in albumin levels

    Time frame: 3 months

    Albumin levels will be measured immediately prior to the procedure, and at one month and three months after the procedure.

  7. Change in Gastric Outlet Obstruction Symptom Score (GOOSS)

    Time frame: 1 year

    The Gastric Outlet Obstruction Symptom Score (GOOSS) scale is as follows, whereas a score of 1 is the worst and a score of 4 is the best:

    • Inadequate or no oral intake
    • Liquids/thickened liquids
    • Semisolids/ low residue
    • Unmodified

    GOOSS will be recorded at each of the following timepoints:

    • immediately prior to the procedure
    • immediately post-procedure
    • 1-day post-procedure
    • 2-days post-procedure
    • 3-days post-procedure
    • 4-days post-procedure
    • 7-days post-procedure,
    • 30-days post-procedure
    • 3-months post-procedure
    • 6-months post-procedure
    • 1-year post-procedure
  8. Change in Gut Function Score (GFS)

    Time frame: 1 year

    Gut Function Score (GFS) scale is as follows, whereas a score of 1 is the worst and a score of 3 is the best:

    • Profuse vomiting
    • Nausea and occasional vomiting
    • Nausea only
    • Normal gut function

    GFS will be recorded at each of the following timepoints:

    • Immediately prior to the procedure
    • Immediately post-procedure
    • 1-day post-procedure
    • 2-days post-procedure
    • 3-days post-procedure
    • 4-days post-procedure
    • 7-days post-procedure,
    • 30-days post-procedure
    • 3-months post-procedure
    • 6-months post-procedure
    • 1-year post-procedure
  9. Karnofsky Performance Scale (KPS)

    Time frame: 30 Days

    Karnofsky Performance Scale is measured on a scale of 0 to 100 as follows, with a score of 0 being the worst and a score of 100 being the best:

    100 - Normal; no complaints; no evidence of disease. 90 - Able to carry on normal activity; minor signs or symptoms of disease. 80 - Normal activity with effort; some signs or symptoms of disease. 70 - Cares for self; unable to carry on normal activity or to do active work. 60 - Requires occasional assistance, but is able to care for most of their personal needs.

    50 - Requires considerable assistance and frequent medical care. 40 - Disabled; requires special care and assistance. 30 - Severely disabled; hospital admission is indicated although death not imminent.

    20 - Very sick; hospital admission necessary; active supportive treatment necessary.

    10 - Moribund; fatal processes progressing rapidly. 0 - Dead

    KPS will be recorded pre-procedure and at 30-days post-procedure.

  10. Chemotherapeutic regimen tolerance

    Time frame: 30 Days

    Ability to tolerate TB approved chemotherapeutic regimen

Study contacts

Contact information is provided by the study sponsor or research team.

Sumbul Yousafi

CONTACT

[email protected]

(718) 470-7983

Sponsors and collaborators

Lead sponsor

Northwell Health

Other

Collaborators

  • Rutgers, The State University of New Jersey

Registry information

Acronym: EAT-GO

Important dates

Study start
2022
Primary completion
2026
Study completion
2027
First posted
Sep 30, 2022
Registry last updated
Jun 15, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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