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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03273686
Other study ID # ESO-NGT
Secondary ID
Status Not yet recruiting
Phase Phase 3
First received September 4, 2017
Last updated September 4, 2017
Start date September 15, 2017
Est. completion date April 15, 2018

Study information

Verified date August 2017
Source Fudan University
Contact Jiaqing Xiang, MD
Phone +86 13901992249
Email j.q.xiang@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Nasogastric decompression is standard practice after esophageal resection in most centers because it is expected to reduce the incidence of esophagogastric anastomotic leakage by preventing overdistension of the gastric conduit. Most esophageal surgeons have been reluctant to move away from this tradition because of the considerable morbidity of anastomotic leaks after esophagectomy. However, a contrarian view is that the use of prolonged NGD may increase the incidence of postoperative pulmonary complications by promoting aspiration. Considering the numerous complications caused by using the tube and the uncertainty about its usefulness and the scarcity of studies conducted on the subject, particularly in patients with esophageal cancer, the necessity of using the tube in these types of cases is investigated in the present study.


Description:

Methods In this clinical trial, patients with esophageal cancer were randomized into groups with NG tube and without NG tube after surgery. Sequence generation was performed using a computer-generated sequence of random numbers with permuted blocks. Standard postoperative management protocols were followed in both groups to avoid potential bias, which including preoperation nasogastric decompression. Thoracic esophageal mobilization and mediastinal lymphadenectomy were performed by open thoracotomy surgery. The abdominal part of the surgery was performed by laparotomy, gastric tube reconstruction was performed using linear staplers, and the conduit was brought up to the neck through the posterior mediastinal route. A cervical esophagogastric anastomosis was performed by stapled (linear) techniques. All patients were mobilized early, began early enteral feeding through jejunostomy tubes. Randomization was performed during the surgery. The group without NG tube after surgery will discharge the NG tube during the surgery. While the control group(group with NG tube after surgery) will discharge the NG tube 6-7days after surgery. The variables recorded for each patient included pulmonary complications, wound complications, anastomosis leak as well as the duration of postoperative hospitalization and the need for placing replacing the NG tube.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date April 15, 2018
Est. primary completion date January 15, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

Patients who were fit for esophageal resection and underwent transthoracic or transhiatal esophagectomy with gastric tube reconstruction.

Exclusion Criteria:

1. Stage investigations indicating unresectable advanced disease(T4 or M1a,M1b).

2. Patients with any other serious underlying medical condition that would impair the ability of the patient to receive or comply with protocol treatment.

3. Patients with unstable situation after surgery (eg, need ventilation and ICU treatment)

4. Patients medically unfit for surgical resection.

5. Patients with pulmonary reserve inadequate to undergo thoracotomy and extensive mediastinal lymphadenectomy.

6. Mentally disabled.

7. Expected life duration of less than 3 months.

8. Patients undergoing colonic reconstruction.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Discharge the NG tube during the surgery
Discharge the NG tube during the surgery.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Fudan University

Outcome

Type Measure Description Time frame Safety issue
Primary postoperative complication the occurrence of major pulmonary complications and anastomotic leaks. an expected average of 4 weeks
Secondary the need for placing/ replacing the NG tube the need for placing/ replacing the NG tube an expected average of 2 weeks
Secondary Length of postoperative stay Length of postoperative stay an expected average of 2 weeks
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