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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03646110
Other study ID # 201804074RINA
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 17, 2018
Est. completion date July 26, 2021

Study information

Verified date November 2020
Source National Taiwan University Hospital
Contact Jang-Ming Lee, MD PhD
Phone +886972651439
Email ntuhlee@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Minimally invasive esophagectomy (MIE) has been gradually adopted as a feasible and effective treatment option for esophageal cancer. Previously the investigators have published the adoption of single-incision approach both in the thoracoscopic and laparoscopic phases in MIE (SIMIE).The preliminary clinical results showed that SIMIE can provide an equivalent perioperative outcome whereas reduced the wound pain on the days 7 after surgery as compared to MIE performed with multi-incision (MIMIE). The goal of the current study was to conduct a prospective randomized trial to compare the perioperative outcome and survival of SIMIE and MIMIE.


Description:

Surgery remains the main stay of treating esophageal cancer. However, esophagectomy is a complex and technical demanding surgical procedure harboring substantial morbidity and mortality. Minimally invasive esophagectomy (MIE) has been gradually adopted as a feasible and effective treatment option for esophageal cancer. The standardized procedure including lymph node dissection, esophageal mobilization and reconstruction can be effectively performed under minimized wound incision whereas rendering the patients a possibility of faster postoperative recovery and reduced risk of perioperative postoperative pulmonary complication. The procedure of MIE including the thoracoscopic and laparoscopic phases which are usually performed multiple incisional wounds. Previously the investigators have published the adoption of single-incision approach both in the thoracoscopic and laparoscopic phases in MIE (SIMIE). The preliminary clinical results showed that SIMIE can provide an equivalent perioperative outcome whereas reduced the wound pain on the days 7 after surgery as compared to MIE performed with multi-incision (MIMIE). The goal of the current study was to conduct a prospective randomized trial to compare the perioperative outcome and survival of SIMIE and MIMIE.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date July 26, 2021
Est. primary completion date July 26, 2021
Accepts healthy volunteers No
Gender All
Age group 35 Years to 75 Years
Eligibility Inclusion Criteria: 1. Patients with a diagnosis of esophageal cancer 2. Age between 35 to 75 years old 3. Resectable tumor as evaluation by preoperative imaging studies. Exclusion Criteria: 1. Previous surgery in the chest or abdomen. 2. Receiving definitive chemoradiation (5500 cGy or more). 3. Tumor invasion to the trachea, spine or aorta. 4. Liver cirrhosis with esophageal varices or liver cirrhosis refractory to medical treatment, Child C classification. 5. Previous history of cerebral vascular attack.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Minimally invasive esophagectomy
Minimally invasive esophagectomy is a surgical procedure for esophageal resection

Locations

Country Name City State
Taiwan Jang-Ming Lee Taipei City Zhongzheng Dist.

Sponsors (1)

Lead Sponsor Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Overall survival rate Overall survival rate of the participants after surgery 60 months
Secondary Pain score as assessed by the face rating scale The scale range of face rating scale is ranging from 0 (happy face) to 10 (crying face). Higher values represent a worse outcome. 1,7,14,28 days
Secondary Ratio of ambulation 30-minute walk test post-operative day 2 (POD2)
Secondary Postoperative force vital capacity Force vital capacity (FVC) is one of the most common parameters for pulmonary function measured in spirometry 1 and 3 months
Secondary Post operative forced expiratory volume in one second Forced expiratory volume in one second (FEV1) is one of the most common parameters for pulmonary function measured in spirometry 1 and 3 months
Secondary Postoperative pulmonary complication pulmonary complication after esophagectomy 1 month
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