CClinicalTrials.gg
CompletedNCT06413888whippleUpdated May 14, 2024

Nasogastric Decompression Following Pancreaticoduodenectomy

An interventional study of pancreaticoduodenectomy in Pancreatic Head Neoplasm, Delayed Gastric Emptying and Post Operative Ileus, sponsored by Baylor College of Medicine. Completed at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-05-14.

Sponsored by Baylor College of Medicine · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 5 years 11 months after the study started (first participant enrolled Jun 2018, registered May 2024).
Phase
Not applicable
Study type
Interventional
Enrollment
230
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Pancreaticoduodenectomy (PD) remains the gold-standard operation for peri-ampullary neoplasms. Traditionally, gastric decompression via nasogastric intubation has been employed postoperatively to prevent nausea, vomiting, aspiration pneumonia, anastomotic leakage and delayed gastric emptying. Recently, the implementation of ERAS protocol recommended against routine use of nasogastric tube following PD. however, limited data exists surrounding the identification of those patients needing NGT decompression in the immediate postoperative period. Therefore, we initiated a large prospective randomized controlled trial to evaluate the clinical outcomes of patients who retained the NGT post-PD versus those who had it removed at the end of the procedure. This study aims to assess the effectiveness of nasogastric decompression in PD recovery, with the primary endo point being the need for and impact of NGT in the postoperative recovery. The secondary endpoint will examined the re-insertion rate of NGT and identify factors that necessitate its use in the immediate postoperative period.

02

Conditions studied

  • Pancreatic Head Neoplasm
  • Delayed Gastric Emptying
  • Post Operative Ileus
  • Whipple Procedure
03

In context

Head and Neck Neoplasms

2,344 studies on the registry are indexed under Head and Neck Neoplasms; 551 are open to participants now.

This study's enrollment of 230 is above the median of 47 across 1,751 interventional studies indexed under Head and Neck Neoplasms.

Browse Head and Neck Neoplasms studies →

Lead sponsor

Baylor College of Medicine is the lead sponsor of 734 studies on the registry; 110 are open to participants now.

Of its 83 completed or terminated interventional studies of FDA-regulated products, 44 (53%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • All patients 18 years of age or older
  • Patients undergoing successful pancreaticoduodenectomy for benign or malignant neoplasm.

Exclusion criteria

Exclusion Criteria:

  • Patients who does not complete the procedure due to locally advanced or metastatic disease discovered during the procedure.
  • Patient who requires prolong postoperative intubation in the postoperative period.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
230 participants (actual)

Study arms

  • Active comparator
    Group A ( No NGT)

    Procedure: pancreaticoduodenectomy

  • Active comparator
    Group B (NGT Retained)

    Procedure: pancreaticoduodenectomy

Interventions

  • Procedurepancreaticoduodenectomy

    Surgical removal of the head of the pancreas, duodenum, extrahepatic bile duct, distal stomach, and proximal jejunum. Group A cohort will not have NGT placed in the postoperative period. Whereas, group B will have the NGT retained in the posoperative period

    Also known as: Whipple

06

What researchers measure

Primary outcomes

  1. to assess whether nasogastric decompression following a whipple procedure will reduce the incidence and severity of postoperative complications

    Severity of post operative complications was graded according to the Clavien-Dindo classification system adopted for pancreaic surgery, which relies on the type of treatment used for each complication with scores range from 1-4, and any complication graded \>2 considered a major complication.

    Time frame: 30-days postoperatively

Secondary outcomes

  1. Examined the re-insertion rate of Nasogastric tube following pancreaticoduodenectomy

    Patient will be considered to undergo nasogastric decompression with nasogastric tube if he/she demonstrated clinical evidence of postoperative ileus and delayed gastric emptying as defined according to the consensus definition proposed by the international study group of pancreatic surgery (ISGPS), the severity of which was classified into 3 grades (A,B, and C) based on clinical course and postoperative management such as the need nausea and vomiting and inability to tolerate solid oral intake by the end of the first postoperative week.

    Time frame: 30- days postoperatively

  2. identify factors that necessitated its use in the immediate postoperative period

    To identify preoperative factors such as obesity with BMI 30 or more, Preoperative uncontrolled diabtes, older age (over 70), gender (male/female), histroy of gastric outlet obstruction, primary diagnosis (malignant disease vs benign). Intra-operative factor such such as the length of the procedure, blood loss, any concurrent procedure such as extensive lysis of adhesions, colon resection; and postoperative factors including postoperative blood counts, phosphorus and magnesium levels, blood sugar level, and postoperative complications. These factors will be assessed using logistic regression analysis to predict the necessity of nasogastric decompression in the postoperative period following the whipple procedure.

    Time frame: 30 days postoperatively

07

Study locations

1 site
  • Baylor college of medicine
    Houston, Texas 77030, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 14, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06413888
Lead sponsor
Baylor College of Medicine
Responsible party
Omar Barakat (Associate Professor, Baylor College of Medicine) — Principal investigator
First posted
May 14, 2024
Start date
Jun 1, 2018
Primary completion
May 31, 2023
Completion
Dec 31, 2023
Last update
May 14, 2024

Study contacts

Omar Barakat, MD
principal investigator · Baylor College of Medicine

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2024. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion