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Gastric Outlet Obstructions Tailored Covered Stents for GOO

T

The First People's Hospital of Yuhang District

Status

Completed

Conditions

Gastric Outlet Obstruction

Treatments

Device: Tailored stents MTN-WE-20/100-A
Device: Standard stents MTN-CG-s-20/100

Study type

Interventional

Funder types

Other

Identifiers

NCT02299258
2011ZHE008

Details and patient eligibility

About

gastric outlet obstruction tailored versus standard stents for malignant gastric outlet obstruction treatments

Full description

To determine the shape of the GOOs, stomach opacifications were performed using contrast media before stenting. In the GOO tailored group (33 cases), the distal stents were semi-spherical with a length of 20 mm and a diameter of 28 mm. The middle stent segments had diameters of 20 mm. The proximal ends of large cup-shaped stents had 53.3 ± 5.5 mm diameters and were 15 or 20 mm long, whereas the large funnel-shaped stents had 33.6 ± 3.6 mm diameters and were 25 or 30 mm long. The control group (32 cases) received standard uncovered stents (semi-spherical, with diameters of 28 mm and 20 mm long).Our hypothesis was that unresectable GOO tailored covered stents are superior to the standard uncovered ones in terms of stent re-obstruction and stent migration. In the current study the efficacy and safety of GOO tailored covered stents for the treatment of non-resectable GOOs caused by distal gastric cancer was compared with standard uncovered stents.

Enrollment

63 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

GOO defined by symptoms resulting in decreased oral intake (nausea, vomiting and inability to eat),the obstruction was caused by primary distal stomach cancer and the site of stenosis was between the gastric body and duodenum bulb

Exclusion criteria

the presence of only mild symptoms in patients who could tolerate a liquid diet, clinical evidence of perforation or peritonitis, evidence of multiple small-bowel obstructions because of peritoneal seeding as well as diabetes or other diseases that affect gastric motility and use of promotility agents.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

63 participants in 2 patient groups

Tailored stents MTN-WE-20/100-A
Active Comparator group
Description:
The distal portion of the GOO tailored stents was semi-spherical, with a length of 20 mm, and a diameter of 28 mm. The middle segment had a diameter of 20 mm. The overall length of the stents was 100 mm. Both the middle part and the bottom of the proximal cup segment, and a part of the proximal funnel segment, were covered by a polyethylene membrane.
Treatment:
Device: Tailored stents MTN-WE-20/100-A
Standard stents MTN-CG-s-20/100
Experimental group
Description:
Standard uncovered stents were used in the control group. The ends of the stents were semi-spherical with diameters of 28 mm and length of 20 mm. The length of the stents was 100 mm
Treatment:
Device: Standard stents MTN-CG-s-20/100

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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