Efficacy of Nasogastric Tube Application in Postoperative Care of Esophagectomy

NCT ID: NCT03273686

Last Updated: 2017-09-06

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE3
• Total Enrollment: 100 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-09-15
• Study Completion Date: 2018-04-15

Brief 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.

Detailed 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.

Conditions

Esophageal Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

group without NG tube after surgery

In this goup, patients will undergo preoperative gastrointestinal decompression and investigators will discharge the NG tube during the surgery.

Group Type: EXPERIMENTAL

Discharge the NG tube during the surgery

Intervention Type: PROCEDURE

Discharge the NG tube during the surgery.

group with NG tube after surgery

In this goup, patients will undergo preoperative gastrointestinal decompression and investigators will discharge the NG tube 6-7 days after the surgery.

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Discharge the NG tube during the surgery

Discharge the NG tube during the surgery.

Intervention Type: PROCEDURE

Eligibility Criteria

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.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Fudan University

OTHER

Sponsor Role: lead

Responsible Party

Jiaqing Xiang

Professor of Department of Thoracic Surgery, Fudan University Shanghai Cancer Center

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Jiaqing Xiang, MD

Role: PRINCIPAL_INVESTIGATOR

Professor of Department of Thoracic Surgery, Fudan University Shanghai Cancer Center

Central Contacts

Jiaqing Xiang, MD

Role: CONTACT

j.q.xiang@hotmail.com

+86 13901992249

Yiliang Zhang, MD

Role: CONTACT

ilya616@126.com

+86 18017317284

Other Identifiers

ESO-NGT

Identifier Type: -

Identifier Source: org_study_id