Clinical Trial Comparing Open and Laparoscopic Nissen Fundoplication in Children
- Conditions
- Gastroesophageal Reflux
- Interventions
- Procedure: Nissen fundoplication
- Registration Number
- NCT00382850
- Lead Sponsor
- Johns Hopkins University
- 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.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 68
- clinical or radiographic diagnosis of gastroesophageal reflux
- age less than 2 years (24 months) at the time of surgery
- 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)
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description open nissen fundoplication Nissen fundoplication open repair through surgical midline incision laparoscopic nissen fundoplication Nissen fundoplication use of laparoscope to do repair
- Primary Outcome Measures
Name Time Method postoperative length of stay 0 to 14days days in hospital
length of time to tolerating full feeds prior to discharge 0 to 7 days days after surgery before feeding begins
postoperative narcotic pain medication requirements 0 to 14 days days requiring narcotics for pain relief
- Secondary Outcome Measures
Name Time Method death up to 2 years death
need for continued medical therapy for GER up to 2 yrs symptomatic reflux requiring medication
wrap failure and need for subsequent reoperation up to 2 yrs operative failure
intraoperative complication rates duration of procedure complications of procedure
Trial Locations
- Locations (1)
Johns Hopkins Hospital
🇺🇸Baltimore, Maryland, United States