Skip to content

Outcome Study of Endoscopically Inserted Gastrostomy (PEG)Versus Radiologically-guided Insertion of Gastrostomy (RIG)in Children

PEG Vs RIG: Percutaneous Endoscopic Gastrostomy Versus Radiologically Inserted Gastrostomy in Children

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01920438
Acronym
PEG Vs RIG
Enrollment
200
Registered
2013-08-12
Start date
2011-12-31
Completion date
2017-08-31
Last updated
2013-08-12

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

Conditions

Two Interventions (PEG and RIG) Compared Against Each Other

Keywords

Percutaneous endoscopic gastrostomy,, Radiologically inserted gastrostomy,, Complications

Brief summary

A gastrostomy is a feeding tube that communicates from the skin directly into the stomach. It is a device frequently used in children that have feeding difficulties or are unable to maintain normal growth via oral feeds. The same device may be inserted in two ways: the percutaneous endoscopic method (PEG) which is guided by the use of an endoscope (flexible camera), or the radiologically inserted method (RIG) which is guided by the use of X-ray imaging. Both methods of insertion have been used in children for more than 20 years, but it is not clear which is the best method. Both methods are associated with complications, including injury to other abdominal organs and leakage leading to sepsis. There are no randomised controlled trials comparing the two techniques. We aim to compare the outcome of both methods of gastrostomy insertion in children, with emphasis on the complication rates. We have devised a complication score with weightage assigned to each complication according to its severity. A randomised controlled trial will be performed in children requiring a gastrostomy, 100 per group. The primary outcome will be the overall total complication rate.

Interventions

PROCEDURERadiologically-guided insertion of Gastrostomy

RIG

Sponsors

Great Ormond Street Hospital for Children NHS Foundation Trust
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* any child referred for gastrostomy insertion

Exclusion criteria

* the child has gastro-esophageal reflux and is being considered for anti-reflux surgery * previous gastrostomy or fundoplication * previous extensive abdominal surgery * the child requires a concomitant major procedure on the gut or other intra- abdominal organs

Design outcomes

Primary

MeasureTime frameDescription
Complication rate3 yearsThe primary end point of the study will be the total number of complications (major and minor).

Secondary

MeasureTime frameDescription
2. minor complication rate : complications not requiring surgery3 yearsInfection requiring systemic antibiotics, delay more than 48 hours in establishing feeds, granulation, wound site discharge, tube-related problems (migration, dislodgement, leakage, breakage), other minor
3.complication score3 yearsThis is a score devised with weighting assigned to each complication depending on the severity of the complication.The score was devised in a consensus meeting attended by experts in the field (paediatric surgeons, interventional radiologists, junior doctors and nurses.
4.technical failure3 yaersThese are the number of PEG or RIG that are unsuccessful and require conversion to open surgical gastrostomy or laparoscopic gastrostomy.
1. major complication rate : complications requiring surgery3 yearsColonic injury or gastro-colic fistula or other visceral injury, peritonitis requiring surgery, intestinal obstruction requiring surgery, major gastrointestinal bleed, other complications requiring surgery
6.cost of hospital treatment3 years
7.mortality3 years
8.cause of death3 years
5.difficulty of procedure3 yearsAssessed by the operator as : 1) easy, 2) slightly difficult (but does not warrant conversion), 3) difficult (warrants conversion)

Countries

United Kingdom

Contacts

Primary ContactRashmi R Singh, MBBS, MRCS
rashmi.singh@ucl.ac.uk02079052682

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026