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NCT Number: NCT07558811

Effects of Glucocorticoid Therapy on Renal Function in Patients With PA Complicated by CKD After Adrenalectomy: A Multicenter RCT

This multicenter randomized controlled trial plans to enroll primary aldosteronism (PA) patients who meet the following criteria: confirmed unilateral dominant secretion by adrenal vein sampling (AVS), willingness to undergo surgery, and coexisting chronic kidney disease (CKD). Participants will be randomly assigned in a 1:1 ratio to one of two groups. To determine whether short-term postoperative hydrocortisone replacement therapy (intervention group) is superior to conventional management (surgery within 7 days after AVS, control group) in terms of reducing the decline in estimated glomerular filtration rate (eGFR) at 12 months after surgery.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Signed and dated informed consent form.
  • Age 18-75 years, any gender.
  • Confirmed diagnosis of primary aldosteronism (PA): positive PA screening test plus positive saline infusion test or captopril challenge test.
  • Imaging findings indicating unilateral adrenal lesion, with adrenal vein sampling (AVS) confirming unilateral dominant secretion consistent with the lesion side, and planned unilateral adrenalectomy.
  • Baseline eGFR 30-60 mL/min/1.73 m² OR positive proteinuria.

Exclusion criteria

  • Use of hydrocortisone within 3 months prior to AVS.
  • eGFR < 30 mL/min/1.73 m², or documented acute kidney injury (AKI) within the past 3 months.
  • Overt cortisol-secreting tumor (clinical Cushing's syndrome) or requirement for long-term hormone replacement therapy.
  • Severe proteinuria (24-hour urinary protein ≥ 3.5 g or ACR ≥ 300 mg/g).
  • NYHA class III-IV heart failure, or acute coronary syndrome or stroke within the past 3 months.
  • Severe allergy to hydrocortisone or history of serious adverse reactions to hydrocortisone.
  • Pregnancy, lactation, or planned pregnancy in the near future.
  • Active malignancy or life expectancy < 1 year.
  • Inability to tolerate surgery.
  • Inability to comply with follow-up as judged by the investigator, or any other condition deemed unsuitable for study participation.

Treatment and study plan

Intervention_1

Drug

Postoperative administration of hydrocortisone for one month

Primary outcomes

  1. the change in eGFR from baseline at 12 months post-surgery

    Time frame: the change in eGFR from baseline at 12 months post-surgery

    To compare the change in eGFR from baseline at 12 months post-surgery between the conventional group and the intervention group.

Sponsors and collaborators

Lead sponsor

Ruijin Hospital

Other

Registry information

Official study title

Effects of Glucocorticoid Therapy on Renal Function in Patients With Primary Aldosteronism Complicated by Chronic Kidney Disease After Adrenalectomy: A Multicenter Randomized Controlled Trial

Acronym: GRAFT_PA

Important dates

Study start
2026
Primary completion
2026
Study completion
2028
First posted
Apr 30, 2026
Registry last updated
Apr 30, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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