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Status unknownNCT03535532ULARHUpdated May 24, 2018

Unilateral Laparoscopic Adrenalectomy for Resistant Hypertension in Patients With Adrenal Diseases

An interventional study of unilateral laparoscopic adrenalectomy and standard medical treatment in Resistant Hypertension and Adrenal Disease, sponsored by Chinese Academy of Medical Sciences, Fuwai Hospital. Status unknown at 3 sites in China. Per ClinicalTrials.gov, last updated 2018-05-24.

Sponsored by Chinese Academy of Medical Sciences, Fuwai Hospital · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified May 2018), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
1,000
Allocation
Randomized
Sex
All
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Study summary

ULARH is a 2-arm, prospective, open-labeled, multi-center randomized clinical trial.The purpose of this study is to compare the effectiveness of medical treatment and unilateral laparoscopic adrenalectomy for resistant hypertension in patients diagnosed with adrenal disease based on imaging tools.Relative ratio of end-point events occurence in three years is considered as primary outcome. Furthermore, we will exploit clinical factors which could indicate a favorable outcome in participants who accepted surgical treatment in this study.

Read the detailed description

Resistant hypertension is a clinical condition characterized by the presence of BP values above the recommended limits of the reference values(BP>140/90 mmHg in hypertensive patients), despite the adherence to appropriate life style changes and to a drug therapy of at least three classes of drugs, one of which is represented by a diuretic, in adequate doses. Several small-sample studies suggest the prevalence of resistant hypertension is about 5-30% in Chinese population. Uncontrolled blood pressure elevation attributes to a higher incidence of stroke, heart failure, chronic renal disease, dementia and cardiovascular deaths. Improving the management of resistant hypertension is a constantly tricky problem in hypertension clinical practice.

Compared with patients whose blood pressure level are more easily to get controlled, patients diagnosed with resistant hypertension presented a higher risk of adrenal anomaly when screened by imaging tools. Current clinical practice guidance recommend unilateral laparoscopic adrenalectomy as a preferable treatment merely for adrenal incidentalomas with over hormone secreting like cortisol or aldosterone, or a high likelihood of malignance. Among patients who meet above surgery indication, the ratio of cure for hypertension varies from approximately 30 to 80%. However, in recent years, there are growing evidence showed that hypertensive patients diagnosed with adrenal disease based on imaging tools also gain much benefit from adrenalectomy even if there is no evidently abnormal hormone secretion. Last year, a prospective cohort study published on \<Ann Intern Med> suggested that "nonfunctional" adrenal tumors associate with increased diabetes risk. These studies prompt a re-assessment of the classification of benign adrenal tumors as "non-functional"and their potential damage.

In a retrospective study conducted by our group in early period to evaluate the effect of surgery treatment in resistant hypertensive patients, we found one third of resistant hypertensive patients were cured as well as another one third get improved after unilateral laparoscopic adrenalectomy. Thus, we designed this study, expecting a further and more detailed perception of the relationship between resistant hypertension and adrenal anomaly.

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Conditions studied

  • Resistant Hypertension
  • Adrenal Disease

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Keywords

  • resistant hypertension
  • Adrenal Disease
  • medical treatment
  • laparoscopic adrenalectomy
03

In context

Adrenal Gland Diseases

24 studies on the registry are indexed under Adrenal Gland Diseases; 9 are open to participants now.

This study's planned enrollment of 1,000 is above the median of 83 across 11 interventional studies indexed under Adrenal Gland Diseases.

Browse Adrenal Gland Diseases studies →

Lead sponsor

Chinese Academy of Medical Sciences, Fuwai Hospital is the lead sponsor of 146 studies on the registry; 50 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Resistant hypertensive patients diagnosed with adrenal disease based on imaging tools (resistant hypertension defined as the presence of BP values above the recommended limits of the reference values(BP>140/90 mmHg),despite the adherence to appropriate life style changes and to a drug therapy of at least three classes of drugs for at least one month, one of which is represented by a diuretic, in adequate doses)
  2. Signed the written informed consent.

Exclusion criteria

Exclusion Criteria:

  1. Patients with surgical contraindication;(Performed coronary revascularization (PCI or CABG) within the previous 6 months; Cerebral hemorrhagic stroke within the previous 3 months, or new onset cerebral infarction within the latest 2 weeks;Severe heart failure or kidney disfunction within the previous 6 months)
  2. Patients who has proceeded unilateral laparoscopic adrenalectomy once;
  3. Severe somatic disease such as cancer;
  4. Severe cognitive impairment or mental disorder;
  5. Participating in other clinical trials.
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
1,000 participants (estimated)

Study arms

  • Experimental
    unilateral laparoscopic adrenalectomy

    subjects allocated in this group will be given unilateral laparoscopic adrenalectomy as treatment.

    Procedure: unilateral laparoscopic adrenalectomy

  • Active comparator
    standard medical treatment

    subjects allocated in standard medical treatment group will be given conservative medicine treatment.

    Drug: standard medical treatment

Interventions

  • Procedureunilateral laparoscopic adrenalectomy

    unilateral laparoscopic adrenalectomy is a kind of minimally invasive surgery commonly operated in patients diagnosed with adrenal diseases with a high likelihood of malignance or surplus hormone secretion.

    Also known as: standard medical treatment

  • Drugstandard medical treatment

    standard medical treatment: detailed medicine strategy chosen for each patient will be associated with their own conditions based on current guidance recommendations.

    Also known as: unilateral laparoscopic adrenalectomy

06

What researchers measure

Primary outcomes

  1. A composite of end-point events

    A composite end-point comprised of myocardial infarction(MI), congestive heart failure, cerebrovascular event, end stage renal disease, death.

    Time frame: 3 year

Secondary outcomes

  1. Major coronary events

    Major coronary events comprised of myocardial infarction (MI), hospitalization for unstable angina or acute decompensated heart failure, coronary revascularization (percutaneous coronary intervention \[PCI\], coronary artery bypass grafting \[CABG\]), and death from cardiovascular causes.

    Time frame: 3 years

  2. First occurrence of symptomatic stroke (ischemic or hemorrhagic, fatal or nonfatal)

    First occurrence of symptomatic stroke (ischemic or hemorrhagic, fatal or nonfatal)

    Time frame: 3 years

  3. All-cause death

    All-cause death

    Time frame: 3 years

  4. Cardiovascular death

    Cardiovascular death

    Time frame: 3 years

  5. myocardial infarction

    myocardial infarction

    Time frame: 3 years

  6. Hospitalization for unstable angina

    Hospitalization for unstable angina

    Time frame: 3 years

  7. Hospitalization for acute decompensated heart failure

    Hospitalization for acute decompensated heart failure

    Time frame: 3 years

  8. coronary revascularization (percutaneous coronary intervention [PCI], coronary bypass grafting [CABG])

    coronary revascularization (percutaneous coronary intervention \[PCI\], coronary bypass grafting \[CABG\])

    Time frame: 3 years

  9. First occurence of diabetes mellitus

    First occurence of diabetes mellitus

    Time frame: 3 years

  10. Decline in cognitive function

    Decline in cognitive function includes sensory disturbance, memory disorders and thinking disorders, which is assessed by mini-mental state examination (MMSE)

    Time frame: 3 years

  11. Decline in renal functio or development of end stage renal disease (ESRD)

    Decline in renal function is assessed by any of the following: (1) For patients with chronic kidney disease (eGFR\<60 ml per minute per 1.73 m2) at baseline, the renal outcome was a composite of a decrease in the eGFR of 50% or more (confirmed by a subsequent laboratory test) or the development of EDRD requiring long-term dialysis or kidney transplantation; or (2) For participants without chronic kidney disease at baseline, the renal outcome was defined by a decreased in the eGFR of 30% or more to a value of less than 60 ml per minute per 1.73 m2.

    Time frame: 3 years

  12. Major artery function changes

    Major artery function changes are assessed by a composite of decrease in the ankle branchial index \[ABI\], brachial-ankle pulse wave velocity(baPWV),or brachial artery flow-mediated dilation \[FMD\]. ABI and baPWV, well-established non-invasive techniques fr evaluating obstruction and stiffness of peripheral artery respectively, are considered for the purposes of cardiovascular risk assessment. ABI is the ratio of average systolic blood pressure measured in brachial/ankle, and an ABI between and including 0.9 and 1.2 is considered normal, while a lesser than 0.9 indicates arterial disease. The unit measure of baPWV value is cm per second. FMD serves as an index of nitric oxide (NO)-mediated endothelium-dependent vasodialator function in humans and is regarded as a surrogate marker of cardiovascular disease.

    Time frame: 3 years

07

Study locations

3 sites
  • Chinese Academy of Medical Sciences, FuWai Hospital
    Beijing, Beijing Municipality 100037, China
    • Jun Cai, MD · Contact
    • Weili Zhang · Contact
    • Jun Cai, MD · Principal investigator
    • Weili Zhang, MD · Principal investigator
  • Shandong Provincial Hospital
    Ji'nan, Shandong 100037, China
    • Shaobo Shaobo · Contact
    • Shaobo Shaobo · Principal investigator
  • Yunzhou Municiple Hospital
    Ji'ning, Shandong, China
    • Xinhai Wang · Contact
    • Xinhai Wang · Principal investigator
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References and documents

Publications

  • Sim JJ, Bhandari SK, Shi J, Reynolds K, Calhoun DA, Kalantar-Zadeh K, Jacobsen SJ. Comparative risk of renal, cardiovascular, and mortality outcomes in controlled, uncontrolled resistant, and nonresistant hypertension. Kidney Int. 2015 Sep;88(3):622-32. doi: 10.1038/ki.2015.142. Epub 2015 May 6. PubMed 25945406 ↗
  • Lopez D, Luque-Fernandez MA, Steele A, Adler GK, Turchin A, Vaidya A. "Nonfunctional" Adrenal Tumors and the Risk for Incident Diabetes and Cardiovascular Outcomes: A Cohort Study. Ann Intern Med. 2016 Oct 18;165(8):533-542. doi: 10.7326/M16-0547. Epub 2016 Aug 2. PubMed 27479926 ↗
  • Xu T, Xia L, Wang X, Zhang X, Zhong S, Qin L, Zhang X, Zhu Y, Shen Z. Effectiveness of partial adrenalectomy for concomitant hypertension in patients with nonfunctional adrenal adenoma. Int Urol Nephrol. 2015 Jan;47(1):59-67. doi: 10.1007/s11255-014-0841-8. Epub 2014 Oct 11. PubMed 25305227 ↗
  • Fassnacht M, Arlt W, Bancos I, Dralle H, Newell-Price J, Sahdev A, Tabarin A, Terzolo M, Tsagarakis S, Dekkers OM. Management of adrenal incidentalomas: European Society of Endocrinology Clinical Practice Guideline in collaboration with the European Network for the Study of Adrenal Tumors. Eur J Endocrinol. 2016 Aug;175(2):G1-G34. doi: 10.1530/EJE-16-0467. PubMed 27390021 ↗
  • Denolle T, Chamontin B, Doll G, Fauvel JP, Girerd X, Herpin D, Vaisse B, Villeneuve F, Halimi JM. [Management of resistant hypertension. Expert consensus statement from the French Society of Hypertension, an affiliate of the French Society of Cardiology]. Presse Med. 2014 Dec;43(12 Pt 1):1325-31. doi: 10.1016/j.lpm.2014.07.016. Epub 2014 Nov 20. French. PubMed 25459067 ↗

Individual participant data

Plan to share: Undecided — Undecided yet

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Dec 2018; primary completion for Oct 2020, 22 months later.

How these figures are worked out, and which studies are left out of them.

Registered
May 14, 2018
First posted
May 24, 2018
StartEst.
Dec 20, 2018
Primary completionEst.
Oct 20, 2020
CompletionEst.
Dec 20, 2021
Last update
May 24, 2018
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 24, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03535532
Responsible party
Jun Cai (Director, Hypertension Center, Chinese Academy of Medical Sciences, Fuwai Hospital) — Principal investigator
First posted
May 24, 2018
Start date
Dec 20, 2018 (estimated)
Primary completion
Oct 20, 2020 (estimated)
Completion
Dec 20, 2021 (estimated)
Last update
May 24, 2018

Study contacts

Weili Zhang, MD
Contact
zhangweili1747@yahoo.com
861088322025
Yue Deng
Contact
dy611381@163.com
861088322025
Jun Cai, MD
study director · Chinese Academy of Medical Sciences, Fuwai Hospital

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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