ClinicalTrials.Veeva

Menu

Copeptin as a Biomarker for Central Diabetes Insipidus Development Following Pituitary Surgery

Mayo Clinic logo

Mayo Clinic

Status

Completed

Conditions

Sellar and Suprasellar Masses
Pituitary Tumor

Study type

Observational

Funder types

Other

Identifiers

NCT04369703
19-010785

Details and patient eligibility

About

  1. Access the optimal cut point value of copeptin which predicts development of central diabetes insipidus postoperatively with highest accuracy.
  2. Access the optimal cut point value of copeptin which predicts the lack of central diabetes insipidus postoperatively with highest accuracy
  3. Access the relative change in copeptin values between baseline and post-surgery as a predictor for diabetes insipidus development.

Full description

Patient serum levels of copeptin would be measured after phlebotomy of 3 ml of blood in EDTA tube twice a) within 1-4 hours of extubation and b) within 4-24 hours of extubation (the morning following surgery).

Enrollment

199 patients

Sex

All

Ages

18 to 95 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

* Patients with sellar and suprasellar masses who undergo neurosurgical procedure at Mayo Clinic Rochester.

Exclusion criteria

* Patients with preexisting CDI.

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems