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Transanal Decompression Tube Versus Stent for Acute Malignant Left-sided Colonic and Rectal Obstruction

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Xuzhou Central Hospital (Xuzhou Fourth People's Hospital)

Status

Terminated

Conditions

Colonic Cancer
Rectal Cancer

Treatments

Device: Stent
Device: Transanal decompression tube

Study type

Interventional

Funder types

Other

Identifiers

NCT02585271
46650455-0

Details and patient eligibility

About

The purpose of this study is to compare the clinical outcomes of transanal decompression tube as a bridge to surgery with stent as a bridge to surgery for acute malignant left-sided colonic and rectal obstruction.

Full description

Approximately 8-47 % of patients with colorectal cancer will present with colonic obstruction. Left-sided colonic and rectal cancer is responsible for nearly 70% of acute colonic obstruction. Emergency colonic surgery for acute obstruction is associated with a higher mortality and morbidity rate than elective surgery. Preoperative decompression results in a less dilated bowel that is more amenable to an elective surgery. Both transanal decompression tube and stent can serve a good preoperative decompression effect and serve a good bridge to surgery. Investigators aim to compare the clinical outcomes of transanal decompression tube as a bridge to surgery with stent as a bridge to surgery for acute malignant left-sided colonic and rectal obstruction.

Enrollment

8 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. definite diagnosis of left-side colonic or rectal obstruction;
  2. symptomatic colonic obstruction for less than 1 week;
  3. colonic obstruction caused by a histologically proven malignant colonic tumor

Exclusion criteria

  1. suspected benign colonic or rectal obstruction;
  2. right-side colonic obstruction;
  3. patients with signs of peritonitis;
  4. dysfunction of blood coagulation, active bleeding, active infection, and significant cardiac or pulmonary disease;
  5. patients who do not want to undergo surgery.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

8 participants in 2 patient groups

Transanal decompression tube
Other group
Description:
Patients undergo placement of the transanal decompression tube as a bridge to surgery
Treatment:
Device: Transanal decompression tube
Stent
Other group
Description:
Patients undergo placement of the stent as a bridge to surgery
Treatment:
Device: Stent

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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