Evaluation of the Autonomic Nervous System in Patients Undergoing Esophagectomy for Cancer
NCT ID: NCT04835987
Last Updated: 2023-11-24
Study Results
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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WITHDRAWN
OBSERVATIONAL
2023-12-31
2024-09-30
Brief Summary
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Detailed Description
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The measurements were taken at night, to overcome the great sympathomimetic variabilities due to external stimulations during the day: one night 3 month before surgery/before the first chemotherapy, one night between 2 and 4 weeks before hospitalization (remotely of possible chemotherapy), the night before the intervention (context of hospitalization and preoperative stress), one night between D7 and D10 (context of hospitalization, and distance from anesthetic drugs), one night at home between 4 and 8 weeks post-operative, and one night at home at 3 months post-operative.
The measurements were therefore not carried out the first nights following the intervention to overcome the anesthetic drugs that affect the balance of the autonomic nervous system.
A baroreflex measurement was carried out at the patient's entrance, the day before the intervention, during hospitalization, and the day of discharge. This measure was renewed at 3 months.
A measurement of patient activity was carried out preoperatively by wearing an actimeter watch for 1 week then renewed at 3 months.
A Respiratory Functional Exploration associated with a stress test with calculation of the VO2max is systematically carried out before the esophageal surgery. A Respiratory Functional Exploration was renewed 4 to 8 weeks after the intervention, and then at 3 months. the 6-minute walk test was performed at the same time.
Conditions
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Study Design
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OTHER
PROSPECTIVE
Interventions
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Questionary
Lifestyle questionary (time spent in front of television, physical activity)
Pupillometry
Monitoring of nociception and autonomic nervous system by pupillometry in intraoperative.
Holter ECG
Measurement of the modification of the sympathomimetic balance
Eligibility Criteria
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Inclusion Criteria
* written and oral agreement
Exclusion Criteria
* patients with permanent atrial fibrillation,
* patients with pace-maker
* Patients under guardianship/curatorship
18 Years
ALL
No
Sponsors
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Centre Hospitalier Universitaire de Saint Etienne
OTHER
Responsible Party
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Principal Investigators
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EVE HUART, MD
Role: PRINCIPAL_INVESTIGATOR
CHU ST ETIENNE
Locations
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Centre Hospitalier Universitaire de Saint-Etienne
Saint-Etienne, , France
Countries
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Other Identifiers
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2020-A03326-33
Identifier Type: OTHER
Identifier Source: secondary_id
20CH250
Identifier Type: -
Identifier Source: org_study_id