RecruitingNot ApplicableNCT05658705

Preoperative Supine Time for Adrenal Venous Sampling

Preoperative Supine Time for Adrenal Venous Sampling: A Prospective Randomized Controlled Trial


Sponsor

Second Affiliated Hospital, School of Medicine, Zhejiang University

Enrollment

120 participants

Start Date

Mar 29, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

This study aim to understand whether the length of preoperative supine time would affect the AVS outcome.


Eligibility

Min Age: 18 YearsMax Age: 80 Years

Inclusion Criteria3

  • Patients are clinically diagnosed as primary aldosteronism with ARR≥37 (PAC showed as pg/ml, renin showed as μIU/mL) and passed through PA confirmatory tests (PAC-post CCT\>110pg/ml, PAC-post SSIT \>80pg/ml, or PAC-post FST\>60pg/ml). PAC: plasma aldosterone concentration;
  • Patients with willing for AVS;
  • Age 18 or above, male or female, with legal capacity.

Exclusion Criteria11

  • Patients with suspected adrenocortical carcinoma or pheochromocytoma;
  • Patients with high risk of adrenal surgery;
  • Patients have been subtyping to glucocorticoid-suppressible hyperaldosteronism or familial hyperaldosteronism type III;
  • Patients were diagnosed as Cushing syndrome or subclinical Cushing syndrome;
  • Patients were treated with glucocorticoids recently;
  • Patients with whole body or venipuncture area infection;
  • Patients with venous access thrombosis;
  • Patients are allergic to iodine;
  • Patients with X-ray contraindications;
  • Patients with coagulation dysfunction;
  • Patients are unable to cooperate and follow-up.

Interventions

PROCEDURE15-min supine time

The length of preoperative supine time before AVS was 15 minutes.

PROCEDURE2-hour supine time

The length of preoperative supine time before AVS was 2 hours.


Locations(1)

The second affiliated hospital of zhejiang university school of medicine

Hangzhou, Zhejiang, China

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT05658705


Related Trials