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NCT04750096: ERASE

Esophagectomy Enhanced Recovery After Surgery Protocol

Status unknown Last updated 11 February 2021
What this trial tests

trial in Esophagectomy in 100 participants. Status unknown.

Timeline
1 September 2020
Primary endpoint
1 September 2022
31 December 2022

Quick facts

Lead sponsorRaquel Ferrandis Comes
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment100
Start date1 September 2020
Primary completion1 September 2022
Estimated completion31 December 2022
Sites1 location across Spain

Conditions studied

Sponsor

Raquel Ferrandis Comes

Who can join

Adults 18 to 90, any sex, with Esophagectomy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Despite the important advances in anaesthesia and the implementation of perioperative care, pulmonary complications in esophagectomy reach figures of between 20 and 35%, and these complications are also closely associated with the mortality rate. Factors that have been associated with the development of respiratory failure in the literature include among others the presence of previous respiratory pathology, history of smoking, malnutrition and rescue surgery. With the aim of improving morbimortality in patients undergoing esophagectomy, a multidisciplinary protocol based on the best scientific evidence at the present time has been implemented, with actions covering both the preoperative and postoperative areas. Based on this point, a prospective study has been designed that allows us to compare the incidence of respiratory failure before and after the implementation of the protocol.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Esophagectomy

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04750096.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing