Influence of Esophageal Washout on Local Carcinoma Recurrence After Curative Resection (LOCARE)
Primary Purpose
Esophageal Neoplasms
Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Povidone-Iodine
Sponsored by
About this trial
This is an interventional prevention trial for Esophageal Neoplasms
Eligibility Criteria
Inclusion Criteria:
- Patients scheduled for elective esophageal resection or esophagectomy
- Age equal or greater than 18 years
- Written informed consent
- Squamous cell carcinoma of the esophagus (SCC)
- Adenocarcinoma of the gastroesophageal junction (AEG) Type I
Exclusion Criteria:
- Local irresectability or metastatic disease
- Adenocarcinoma of the gastroesophageal junction Type II and III
- Histopathological R1-resection
- Surgery for recurrence
- Iodine allergy
- Hyperthyreosis
Sites / Locations
- Department of GI, Thoracic and Vascular Surgery, University Hospital Carl Gustav Carus, TU Dresden
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
A (Povidone-Iodine)
B (Control)
Arm Description
Esophageal washout will be performed via a nasogastric tube with approx. 50ml of a 11% povidone-iodine solution (Betaisodona®, Mundipharma) during esophageal resection.
Esophageal resection will be performed without esophageal washout.
Outcomes
Primary Outcome Measures
Local carcinoma recurrence
Defined as development of a local recurrence after surgical treatment for esophageal cancer. The tumor is of identical histopathological type and occurs either on remained parts of the esophagus, at the site of anastomosis, on parts of an interposed organ (i.e. jejunum or colon) or in the original esophageal bed.
Secondary Outcome Measures
Full Information
NCT ID
NCT02676791
First Posted
February 4, 2016
Last Updated
July 13, 2022
Sponsor
Technische Universität Dresden
1. Study Identification
Unique Protocol Identification Number
NCT02676791
Brief Title
Influence of Esophageal Washout on Local Carcinoma Recurrence After Curative Resection
Acronym
LOCARE
Official Title
Influence of Esophageal Washout on Local Carcinoma Recurrence After Curative Resection - a Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
July 2022
Overall Recruitment Status
Completed
Study Start Date
February 16, 2016 (Actual)
Primary Completion Date
September 24, 2021 (Actual)
Study Completion Date
September 24, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Technische Universität Dresden
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The LOCARE-Trial is an investigator initiated, randomized-controlled trial with two parallel arms (n=60 each) and investigates the influence of esophageal washout on long-term outcomes in patients undergoing elective esophageal resection for carcinoma. The primary endpoint is defined as local carcinoma recurrence. Secondary endpoints will be locoregional and distant recurrence, disease-specific survival and esophageal cancer specific survival.
Detailed Description
Treatment of squamous cell carcinoma and adenocarcinoma of the esophagus has changed rapidly over the last decades due to implementation of multimodal cancer therapies such as radiotherapy or combined radiochemotherapy. Surgery, however, still is the mainstay of curative treatment options for this cancer entity. Due to the significant improvement in surgical technique and perioperative management, the postoperative mortality rate has fallen to about 5% with an estimated 5-year survival of 35%. Nevertheless, patients after esophagectomy are at high risk for local recurrence especially within the first 2 years after treatment. Independent risk factors for the development of carcinoma recurrence are incomplete resection (R1), extracapsular lymph node involvement and postoperative complications. Exfoliated, malignant cells remaining in luminal organs like the esophagus or colorectum could present another important risk factor for local recurrence especially at the site of anastomosis. In the treatment of rectal cancer, data have shown, that intraoperative rectal washout significantly reduces the risk of local recurrence from about 10% to 5%. For this reason, rectal washout during anterior resection has become a standard in many surgical institutions. Besides agents like cetrimide, sodium hypochlorite, formalin or saline, povidone-iodine has also been used for rectal mucosal application in prospective studies. Questions arise, weather similar positive outcomes could be achieved in esophageal surgery. The investigators hypothesize that esophageal washout with a povidone-iodine solution (Betaisodona®, Mundipharma) reduces the risk of local carcinoma recurrence after radical resection.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Esophageal Neoplasms
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
80 (Actual)
8. Arms, Groups, and Interventions
Arm Title
A (Povidone-Iodine)
Arm Type
Experimental
Arm Description
Esophageal washout will be performed via a nasogastric tube with approx. 50ml of a 11% povidone-iodine solution (Betaisodona®, Mundipharma) during esophageal resection.
Arm Title
B (Control)
Arm Type
No Intervention
Arm Description
Esophageal resection will be performed without esophageal washout.
Intervention Type
Drug
Intervention Name(s)
Povidone-Iodine
Other Intervention Name(s)
Betaisodona
Intervention Description
A standard nasogastric tube will be inserted into all patients after induction of general anesthesia. After surgical dissection, the esophagus / stomach will be cut at the desired level leaving the tip of the nasogastric tube proximal to the esophageal carcinoma. Then, 50ml of a 11% povidone-iodine solution (Betaisodona®, Mundipharma) will be introduced into the esophagus via the nasogastric tube and evacuated with a suction device (washout). The nasogastric tube will then be removed for completion of esophageal resection and beginning of reconstruction.
Primary Outcome Measure Information:
Title
Local carcinoma recurrence
Description
Defined as development of a local recurrence after surgical treatment for esophageal cancer. The tumor is of identical histopathological type and occurs either on remained parts of the esophagus, at the site of anastomosis, on parts of an interposed organ (i.e. jejunum or colon) or in the original esophageal bed.
Time Frame
36 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients scheduled for elective esophageal resection or esophagectomy
Age equal or greater than 18 years
Written informed consent
Squamous cell carcinoma of the esophagus (SCC)
Adenocarcinoma of the gastroesophageal junction (AEG) Type I
Exclusion Criteria:
Local irresectability or metastatic disease
Adenocarcinoma of the gastroesophageal junction Type II and III
Histopathological R1-resection
Surgery for recurrence
Iodine allergy
Hyperthyreosis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christoph Reißfelder, MD
Organizational Affiliation
Department of GI, Thoracic and Vascular Surgery, University Hospital Carl Gustav Carus, TU Dresden
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of GI, Thoracic and Vascular Surgery, University Hospital Carl Gustav Carus, TU Dresden
City
Dresden
Country
Germany
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Influence of Esophageal Washout on Local Carcinoma Recurrence After Curative Resection
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