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Clinical Trial Comparing Open and Laparoscopic Nissen Fundoplication in Children

Primary Purpose

Gastroesophageal Reflux

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Nissen fundoplication
Sponsored by
Johns Hopkins University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gastroesophageal Reflux focused on measuring Nissen fundoplication, gastroesophageal reflux

Eligibility Criteria

undefined - 24 Months (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • clinical or radiographic diagnosis of gastroesophageal reflux
  • age less than 2 years (24 months) at the time of surgery

Exclusion Criteria:

  • prior fundoplication procedure
  • concomitant need for an intraabdominal procedure (except gastrostomy tube placement)
  • esophageal dysmotility
  • hospitalization expected to be prolonged due to a concurrent illness actively being treated (e.g. congenital heart disease requiring surgical repair during the same hospitalization)

Sites / Locations

  • Johns Hopkins Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

open nissen fundoplication

laparoscopic nissen fundoplication

Arm Description

open repair through surgical midline incision

use of laparoscope to do repair

Outcomes

Primary Outcome Measures

postoperative length of stay
days in hospital
postoperative narcotic pain medication requirements
days requiring narcotics for pain relief
length of time to tolerating full feeds prior to discharge
days after surgery before feeding begins

Secondary Outcome Measures

intraoperative complication rates
complications of procedure
wrap failure and need for subsequent reoperation
operative failure
need for continued medical therapy for GER
symptomatic reflux requiring medication
death
death

Full Information

First Posted
September 29, 2006
Last Updated
July 30, 2018
Sponsor
Johns Hopkins University
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1. Study Identification

Unique Protocol Identification Number
NCT00382850
Brief Title
Clinical Trial Comparing Open and Laparoscopic Nissen Fundoplication in Children
Official Title
Randomized Controlled Trial of Laparoscopic Compared to Open Nissen Fundoplication in Children Younger Than 2 Years of Age
Study Type
Interventional

2. Study Status

Record Verification Date
July 2018
Overall Recruitment Status
Completed
Study Start Date
November 2005 (undefined)
Primary Completion Date
November 30, 2010 (Actual)
Study Completion Date
November 30, 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Johns Hopkins University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine whether short- and long-term outcomes are different between open and laparoscopic Nissen fundoplication performed in children younger than 2 years of age.
Detailed Description
Nissen fundoplication is a commonly performed procedure in infants and children with gastroesophageal reflux and a variety of other medical conditions including respiratory compromise, severe neurologic impairment, failure to thrive and swallowing dysfunction. Randomized controlled trials in adults have shown that laparoscopic fundoplication is a safe procedure that results in lower morbidity, shorter hospital length of stay and similar 5-year recurrence rates when compared to an open procedure. The aim of this study is to compare laparoscopic and open Nissen fundoplication in children less than 2 years of age. Children younger than 2 years of age presenting for Nissen fundoplication will be randomized to either a laparoscopic or an open procedure. Patients who have already undergone anti-reflux surgery or whose hospitalization is anticipated to be prolonged by an unrelated illness will be excluded. All procedures will be performed at a single institution by two surgeons who will perform both the open and laparoscopic procedures. A total of 68 patients will be needed (34 in each group) to detect a 20% difference in length of stay at a significance level of p < 0.05 and power of 80%. Patients will be followed for up to 2 years postoperatively. Variables to be compared between the two groups will include age, gender, presence of neurologic impairment, presence and specification of any congenital abnormalities, total operative time, total dose of narcotic analgesia required, postoperative day on which the patient tolerated full feedings, postoperative and total lengths of stay as well as the occurrence of postoperative complications (including wound infection and the need for immediate reoperation). The primary outcomes analyzed will be length of stay and amount of narcotic analgesia required. Longer-term outcomes including persistent GERD, wrap failure and need for reoperation within 24 months of the initial procedure also will be determined.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastroesophageal Reflux
Keywords
Nissen fundoplication, gastroesophageal reflux

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Care Provider
Allocation
Randomized
Enrollment
68 (Actual)

8. Arms, Groups, and Interventions

Arm Title
open nissen fundoplication
Arm Type
Active Comparator
Arm Description
open repair through surgical midline incision
Arm Title
laparoscopic nissen fundoplication
Arm Type
Active Comparator
Arm Description
use of laparoscope to do repair
Intervention Type
Procedure
Intervention Name(s)
Nissen fundoplication
Primary Outcome Measure Information:
Title
postoperative length of stay
Description
days in hospital
Time Frame
0 to 14days
Title
postoperative narcotic pain medication requirements
Description
days requiring narcotics for pain relief
Time Frame
0 to 14 days
Title
length of time to tolerating full feeds prior to discharge
Description
days after surgery before feeding begins
Time Frame
0 to 7 days
Secondary Outcome Measure Information:
Title
intraoperative complication rates
Description
complications of procedure
Time Frame
duration of procedure
Title
wrap failure and need for subsequent reoperation
Description
operative failure
Time Frame
up to 2 yrs
Title
need for continued medical therapy for GER
Description
symptomatic reflux requiring medication
Time Frame
up to 2 yrs
Title
death
Description
death
Time Frame
up to 2 years

10. Eligibility

Sex
All
Maximum Age & Unit of Time
24 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: clinical or radiographic diagnosis of gastroesophageal reflux age less than 2 years (24 months) at the time of surgery Exclusion Criteria: prior fundoplication procedure concomitant need for an intraabdominal procedure (except gastrostomy tube placement) esophageal dysmotility hospitalization expected to be prolonged due to a concurrent illness actively being treated (e.g. congenital heart disease requiring surgical repair during the same hospitalization)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paul M Colombani, MD
Organizational Affiliation
Johns Hopkins University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Johns Hopkins Hospital
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21287
Country
United States

12. IPD Sharing Statement

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Clinical Trial Comparing Open and Laparoscopic Nissen Fundoplication in Children

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