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Monitoring of Glycocalyx for Prediction of Complications After Cardiac Surgery (MOGLYCC)

U

University Hospital, Rouen

Status

Enrolling

Conditions

Cardiac Surgery

Study type

Observational

Funder types

Other

Identifiers

NCT06136637
2021-A02377-34
2020/416/OB (Other Identifier)

Details and patient eligibility

About

This is a prospective observational study of the evolution of the microcirculation and the sublingual glycocalyx in perioperative cardiac surgery under cardiopulmonary bypass. Our main objective is to evaluate the prognostic value of the variation of the thickness of the perioperative glycocalyx for the occurrence of a major complication in the first 24 hours after surgery.

Enrollment

77 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

  • Patient of legal age (age ≥ 18 years)
  • Patient undergoing scheduled cardiac surgery with cardiopulmoary bypass (CPB) (expected duration of CPB > 60 min)
  • Person informed with collection of non-opposition at the latest, the day before the operation - Person affiliated to a social security system

Trial contacts and locations

1

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Central trial contact

Demailly Zoé, MD; DRCI Rouen

Data sourced from clinicaltrials.gov

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