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Combined Thoracoscopic and Laparoscopic Esophagectomy vs. Hand-assisted Transhiatal Esophagectomy: A Prospective Trial.

Primary Purpose

Adenocarcinoma

Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Laparoscopic Esophagectomy
Sponsored by
University of California, Irvine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Adenocarcinoma focused on measuring Adenocarcinoma, Esophagectomy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patients with biopsy proven esophageal malignancies Patients with recalcitrant severe esophageal stricture Karnofsky score >60 No previous treatment for any other cancer over the past 2 years (except for skin cancer) Exclusion Criteria: Malignant tracheoesophageal fistula or presence of tracheal involvement Unacceptable operative risk Tumor size greater than 12 centimeters. Tumor involvement of the aorta or trachea. Renal or liver insufficiency (Creatinine > 2.0, transaminase > fourfold) WBCs <2,000, platelets <80,000 Presence of metastatic disease Patients with previous esophageal resection Minors and pregnant women are excluded. The chance of esophageal cancer presenting in anyone under 18 years of age is essentially null. Pregnant women are excluded because of safety for the fetus. All physician, hospital, surgery, and laboratory costs will be billed to the subject and/or their insurance carrier as customary for they are considered standard of care procedures. All research-related procedures such as pulmonary function tests and study questionnaires conducted in this study will be paid for by the primary investigator.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Active Comparator

    Arm Label

    1

    2

    Arm Description

    Combined Thoracoscopic and Laparoscopic Esophagectomy

    Hand-Assisted Transhiatal Esophagectomy

    Outcomes

    Primary Outcome Measures

    short-term surgical outcome of minimally invasive esophagectomy vs. transhiatal esophagectomy

    Secondary Outcome Measures

    long-term surgical outcome of minimally invasive esophagectomy vs. transhiatal esophagectomy.

    Full Information

    First Posted
    October 31, 2005
    Last Updated
    January 22, 2021
    Sponsor
    University of California, Irvine
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00247936
    Brief Title
    Combined Thoracoscopic and Laparoscopic Esophagectomy vs. Hand-assisted Transhiatal Esophagectomy: A Prospective Trial.
    Official Title
    Combined Thoracoscopic and Laparoscopic Esophagectomy vs. Hand-assisted Transhiatal Esophagectomy: A Prospective Trial.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    January 2021
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    Prior to recruitment, study terminated lack of recruitment interest.
    Study Start Date
    May 2004 (undefined)
    Primary Completion Date
    May 2004 (Actual)
    Study Completion Date
    May 2004 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    University of California, Irvine

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Esophagectomy for benign or malignant disease of the esophagus can be performed using a transhiatal technique or Ivor Lewis technique (combined laparotomy with thoracotomy). These procedures can be associated with significant morbidity and mortality [1]. Advances in minimally invasive technology and surgical techniques have allowed us to explore the possibility of performing esophagectomy using minimally invasive surgical techniques. Minimally invasive esophagectomy represents a new alternative to conventional open esophagectomy. It is a technically demanding operation requiring advanced laparoscopic surgical skills, appropriate instrumentation, and thorough knowledge of open esophagectomy. Multiple authors have reported the use of video-assisted thoracoscopy or laparoscopy to facilitate esophagectomy [2-6]. Most of these reports have utilized a standard laparotomy in combination with thoracoscopy to perform esophageal mobilization or laparoscopy with a mini-laparotomy to perform esophagectomy. DePaula was the first to report a large series of 48 patients undergoing laparoscopic transhiatal esophagectomy for benign (n=24) and malignant disease (n=24) [7]. In 2 patients, conversion to open surgery was required and 2 others required thoracoscopic assistance. Postoperative complications were low in the benign group but higher in the carcinoma group. The 30-day mortality rate was 16% in patients with carcinoma undergoing laparoscopic transhiatal esophagectomy. DePaula concluded that the patients who benefit most from this procedure are those with benign disease. Swanstrom recently reported nine cases of laparoscopic total esophagectomy [8]. There were no conversions to laparotomy. One patient required a right thoracoscopy with intrathoracic anastomosis due to poor viability of the gastric tube. The mean operative time was 6.5 hours with a mean hospital stay of 6.4 days. However, the advantages of minimally invasive esophagectomy have not been observed. The aim of this prospective trial is to evaluate the physiologic outcome, clinical outcome, and quality of life after combined thoracoscopic and laparoscopic esophagectomy vs. transhiatal esophagectomy.
    Detailed Description
    RATIONALE: Open esophagectomy can be associated with significant morbidity. We hypothesize that laparoscopic esophagectomy is associated with reduced morbidity and a faster recovery. HYPOTHESES: Combined thoracoscopic and laparoscopic esophagectomy can be performed safely. Combined thoracoscopic and laparoscopic esophagectomy is associated with reduced postoperative pain, decrease ICU and hospital stay, and reduced postoperative wound morbidity. Combined thoracoscopic and laparoscopic esophagectomy is associated with similar long term survival as with the open approach for patients with esophageal malignancies. OBJECTIVES AND SPECIFIC AIMS: To compare short-term outcome such as operative time, operative and in-patient costs, operative complications, length of hospital stay, and postoperative complications between combined thoracoscopic/ laparoscopic esophagectomy and transhiatal esophagectomy. To evaluate physiologic outcomes after minimally invasive esophagectomy vs. transhiatal esophagectomy. To determine the long-term outcome, disease-free survival, survival and quality of life after minimally invasive esophagectomy compared to transhiatal esophagectomy

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Adenocarcinoma
    Keywords
    Adenocarcinoma, Esophagectomy

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Non-Randomized
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    1
    Arm Type
    Active Comparator
    Arm Description
    Combined Thoracoscopic and Laparoscopic Esophagectomy
    Arm Title
    2
    Arm Type
    Active Comparator
    Arm Description
    Hand-Assisted Transhiatal Esophagectomy
    Intervention Type
    Procedure
    Intervention Name(s)
    Laparoscopic Esophagectomy
    Other Intervention Name(s)
    Laparoscopic Esophagectomy; Hand-Assisted Transhiatal Esophagectomy
    Intervention Description
    Laparoscopic Esophagectomy
    Primary Outcome Measure Information:
    Title
    short-term surgical outcome of minimally invasive esophagectomy vs. transhiatal esophagectomy
    Time Frame
    30-day
    Secondary Outcome Measure Information:
    Title
    long-term surgical outcome of minimally invasive esophagectomy vs. transhiatal esophagectomy.
    Time Frame
    5 year

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients with biopsy proven esophageal malignancies Patients with recalcitrant severe esophageal stricture Karnofsky score >60 No previous treatment for any other cancer over the past 2 years (except for skin cancer) Exclusion Criteria: Malignant tracheoesophageal fistula or presence of tracheal involvement Unacceptable operative risk Tumor size greater than 12 centimeters. Tumor involvement of the aorta or trachea. Renal or liver insufficiency (Creatinine > 2.0, transaminase > fourfold) WBCs <2,000, platelets <80,000 Presence of metastatic disease Patients with previous esophageal resection Minors and pregnant women are excluded. The chance of esophageal cancer presenting in anyone under 18 years of age is essentially null. Pregnant women are excluded because of safety for the fetus. All physician, hospital, surgery, and laboratory costs will be billed to the subject and/or their insurance carrier as customary for they are considered standard of care procedures. All research-related procedures such as pulmonary function tests and study questionnaires conducted in this study will be paid for by the primary investigator.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Ninh T Nguyen, MD
    Organizational Affiliation
    University of California, Irvine
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

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    Combined Thoracoscopic and Laparoscopic Esophagectomy vs. Hand-assisted Transhiatal Esophagectomy: A Prospective Trial.

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