Short-term Outcomes of ERAS Protocol in RAME for Esophageal Cancer

NCT ID: NCT05600335

Last Updated: 2022-11-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

211 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-01-01

Study Completion Date

2022-03-09

Brief Summary

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This single-center, retrospective cohort study aimed to evaluate the short-term outcomes of enhanced recovery after surgery (ERAS) protocol in perioperative robotic-assisted McKeown esophagectomy (RAME) among esophageal cancer patients.

Detailed Description

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Conditions

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Esophageal Cancer Patients

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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ERAS group

ERAS protocol

Intervention Type PROCEDURE

Patients with esophageal cancer have undergone RAME using ERAS protocol and conventional management strategy

Conventional group

ERAS protocol

Intervention Type PROCEDURE

Patients with esophageal cancer have undergone RAME using ERAS protocol and conventional management strategy

Interventions

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ERAS protocol

Patients with esophageal cancer have undergone RAME using ERAS protocol and conventional management strategy

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

1. first detected and endoscopically confirmed esophageal cancer;
2. preoperative evaluation showed no distant metastases and suitable for RAME;
3. preoperative clinical stage of I to III;

Exclusion Criteria

1. patients had a history of thoracic or abdominal surgery;
2. patients were IV to VI in the American Society of Anesthesiologists (ASA) physical status classification system;
3. patients had other malignancies;
4. patients had missing clinical data
Minimum Eligible Age

20 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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West China Hospital

OTHER

Sponsor Role lead

Responsible Party

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Jiajun Xiong

MD

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Yidan Lin, MD

Role: STUDY_DIRECTOR

West China Hospital

Locations

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West China Hospital of Sichuan University

Chengdu, Sichuan, China

Site Status

Countries

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China

Other Identifiers

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HXDB-1908

Identifier Type: -

Identifier Source: org_study_id

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