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A Modified Method for Blind Bedside Placement of Post-pyloric Feeding Tube.

Zhejiang University logo

Zhejiang University

Status

Completed

Conditions

Nutritional Support, Catheterization, Post-pyloric Feeding Tube, Dysphagia

Treatments

Procedure: A modified method for blind bedside placement of post-pyloric feeding tube.

Study type

Observational

Funder types

Other

Identifiers

NCT04608071
2020-273

Details and patient eligibility

About

To compare efficacy and safety of a new modified post-pyloric feeding tube bedside catheterization with Corpak 10-10-10 protocol and electromagnetic guided catheterization for treatment of patients with dysphagia and at high-risk of aspiration pneumonia. We conducted a single-center, single-blinded, and randomized controlled clinical trial. A total of 63 patients were treated with the non-gravity type CORFLO gastrointestinal feeding tube between 2017.1 and 2019.1 using different procedures: in the M group, patients underwent modified post-pyloric feeding tube bedside placement; in C group, patients underwent conventional Corpak protocol; in EM group, patients received standard electromagnetic guided tube placement.

Enrollment

99 patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All patients had dysphagia that could not be alleviated within 48 hours
  • High-risk status with aspiration pneumonia, including consciousness disorder caused by various diseases, severe dementia, bed rest, gastroesophageal reflux, hiccup, gastric retention, achalasia of pyloric.
  • Can't receive nasogastric tube feeding.

Exclusion criteria

  • The previous history of upper abdominal surgery.
  • Gastroduodenal ulcer and esophagogastric varices;
  • Severe sinusitis and nasal bone fracture;
  • Patients with recent gastrointestinal bleeding, intestinal obstruction, ischemic bowel disease, and epistaxis;
  • Patients with electromagnetically-guided catheterization should additionally exclude implantable cardiac defibrillator, implantable cardiac pacemaker or diaphragm pacemaker.

Trial design

99 participants in 3 patient groups

M group
Description:
In M group, patients underwent modified post-pyloric feeding tube bedside placement
Treatment:
Procedure: A modified method for blind bedside placement of post-pyloric feeding tube.
C group
Description:
In C group, patients underwent conventional Corpak protocol
Treatment:
Procedure: A modified method for blind bedside placement of post-pyloric feeding tube.
EM group
Description:
In EM group, patients received standard electromagnetic guided tube placement.
Treatment:
Procedure: A modified method for blind bedside placement of post-pyloric feeding tube.

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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