POsitioning for Esophageal Cancer Resection

Not Applicable

Terminated

• Conditions: Esophageal Cancer

• Registration Number: NCT02157363
• Lead Sponsor: Technische Universität Dresden

Brief Summary

Open thoracoabdominal esophagectomy (TAE) is the standard curative treatment modality for resectable esophageal cancer. TAE can be achieved by positioning the patient in the supine position for the abdominal part and in a left-lateral decubitus (LLD) position for the thoracic part, or by performing both parts in a left-screwed supine position (LSS). Aim of the present study is to compare peri- and postoperative outcome variables after TAE for esophageal cancer in the two positions.

POETRI is designed as a single-center, randomized controlled trial with two parallel arms including patients with resectable esophageal cancer and type I cancers of the esophagogastric junction (AEG I). Exclusion criteria are inability to tolerate surgery or both types of positioning, inability to perform an intrathoracic anastomosis, non-malignant pathologies. The primary endpoint is operating time. Secondary endpoints are morbidity, lymph node yield, pulmonary function, pain control and wound healing assessed during a follow-up of 3 months.

POETRI is a single-center, randomized controlled trial to evaluate different positioning and thoracic access during radical open thoracoabdominal esophagectomy for patients with resectable esophageal cancer.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2014-05-12
• Study First Submitted QC: 2014-06-02
• Study First Posted: 2014-06-06
• Study Start: 2014-06-16
• Primary Completion: 2017-02-28
• Study Completion: 2017-02-28
• Status Verified: 2017-10
• Last Update Submitted: 2017-10-19
• Last Update Posted: 2017-10-20

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 47

Inclusion Criteria

• Newly diagnosed, non-metastatic esophagus cancer (squamous or adenocarcinoma) or AEG I tumors requiring curative thoracoabdominal esophagectomy with intrathoracic anastomosis of a gastric tube immediately after diagnosis or after neoadjuvant treatment
• Patients are considered fit for surgery by a local interdisciplinary team of surgeons, medical oncologists and anesthesiologists (ECOG performance status of 0,1, or 2).
• Age ≥ 18 years
• Written informed consent

Exclusion Criteria

• Preoperative established indication for colon interposition or cervical anastomosis
• Preoperative diagnosed tracheo-esophageal fistula
• History of right thoracotomy or prior lung surgery
• Physical inability of the described intraoperative patient positioning
• Non-malignant esophageal pathology or other malignancies except squamous or adenocarcinoma
• Planned laparoscopic or thoracoscopic surgical approach
• Patients not eligible for TAE (ASA ≥ 4)

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
operating time	The endpoint is assessed at the end of the operation (finishing of all wound dressings) on the day of operation.	Operating time is defined from the start of patient positioning until final closing and dressing of all wounds.

Trial Locations

Locations (1)

Department of Surgery, University Hospital Dresden; 🇩🇪 Dresden, Germany