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The primary objective of WAVE is to test the hypothesis that thermal ablation (microwave or RFA) is non-inferior to surgery in the biochemical (and if so, in the clinical) cure of unilateral PA, according to the international consensus PASO criteria.
Secondary objectives are to determine whether either intervention is superior to the other in relation to the following outcomes. Where no superiority of either intervention is established, non-inferiority of thermal ablation against adrenalectomy will be sought.
An additional secondary objective in the thermal ablation group alone will be anatomical efficacy of ablation.
Primary aldosteronism (PA) results from renin-independent aldosterone hypersecretion and causes hypertension, often with associated hypokalaemia and metabolic alkalosis. These are due to enhanced mineralocorticoid receptor-mediated renal sodium retention and potassium excretion. PA is the commonest cause of secondary hypertension and is responsible for 5-10% of all hypertension, rising to in excess of 20% of resistant cases. Very low diagnosis rates result from a generation of doctors schooled on order-of-magnitude lower estimates, but recent findings suggest that even the 5-10% prevalence may be a considerable under-estimate. In addition to its frequency, PA is a high-risk subset of hypertension and is associated with a two-fold increased risk of cardiovascular events and atrial fibrillation compared to comparable patients with essential hypertension, as well as a reduced quality of life.
Aldosterone excess in PA can originate from one or both adrenal glands. Patients with PA are considered to divide ~50:50 into those with a curable unilateral aldosterone-producing adenoma (APA), and those with bilateral idiopathic adrenal hyperplasia (IAH). For patients with unilateral PA, surgical removal of the affected gland (adrenalectomy) is highly likely to cure the biochemical abnormality, reverse the excess cardiovascular and stroke risks, and is strongly supported by international guidelines.
Whilst directed medical therapies against aldosterone excess exist (e.g. mineralocorticoid receptor antagonists, MRAs), they are inferior to surgery in reducing the excess cardiovascular and stroke risk and improving quality of life. Furthermore, sufficient MRA dosing to de-suppress renin and reverse this excess risk is only achieved in one-third of medically-treated patients. The case for definitive intervention in unilateral PA is therefore compelling, and recommended whenever possible. At present, this is achieved by laparoscopic adrenalectomy (LA), which involves a general anaesthetic, inpatient admission and removal of the entire adrenal gland to treat a condition caused by a small (usually <2cm diameter, often <1cm) benign APA.
An alternative intervention to LA, and the focus of this trial, is selective thermal ablation (by radiofrequency or microwave) of the identified APA(s). Thermal ablation is a technique in which targeted and directed tissue death can be achieved with precision under image guidance, sparing the normal adrenal gland. It is widely established in the treatment of benign and malignant hepatic and renal neoplasms as an alternative to conventional surgery. For these indications, thermal ablation techniques have transformed practice, not only providing high-risk surgical patients with a previously unobtainable curative treatment option but also becoming an accepted mainstay of treatment for small lesions (of the size encountered in PA) in all patients regardless of surgical risk.
We propose a multi-centre prospective randomised trial comparing adrenalectomy (LA) and thermal ablation for the treatment of unilateral APAs. This study is powered to demonstrate non-inferiority of biochemical and clinical response to thermal ablation, compared to the current standard of care, adrenalectomy. The rationale for a non-inferiority trial is that subsequent preference for thermal ablation over surgery will be driven by thermal ablation's greater patient-acceptability and availability, rather than an implausible superior efficacy of sub-total than total adrenalectomy in curing PA. Once safety and efficacy are proven as comparable to those of adrenalectomy, thermal ablation has potential for superiority over medical treatment in several patient groups ineligible for WAVE, e.g., some with bilateral disease, or in whom lateralisation could not be performed.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Thermal ablation of adrenal aldosterone producing adenoma (s) | Experimental | For patients randomized to ablation, thermal ablation (either microwave or radiofrequency ablation) will be deployed to treat the adrenal aldosterone producing adenoma(s) |
|
| Unilateral adrenalectomy for aldosterone producing adenoma (s) | Other | For patients randomized to surgery, unilateral adrenalectomy will be performed to remove aldosterone producing adenoma(s) |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Thermal ablation of aldosterone producing adenoma. | Procedure | On the left side, Radiofrequency ablation of aldosterone producing adenoma(s) will be undertaken via the stomach (endoscopically), under transgastric ultrasound guidance. On the right side, either Radiofrequency or Microwave Ablation of aldosterone producing adenoma(s) will be performed via a percutaneous approach, under CT guidance. |
| Measure | Description | Time Frame |
|---|---|---|
| Complete biochemical cure of PA | Complete biochemical cure of PA, defined (whilst off medications that might alter serum potassium or the RAS) by both:
i. Baseline PAC <190pmol/L, or ii. Normal confirmatory test (as defined in the inclusion criteria) | 6 months post intervention |
| Complete clinical cure of PA | Complete clinical cure of PA, defined as normotension without antihypertensive medication These criteria have been defined in the international consensus PASO statement8, which has become the established yardstick by which PA cure is judged. In this, normotension is defined, in accordance with the European Society of Hypertension guidelines22, as <140/80 in the office, <135/85 at home or daytime ambulatory monitoring and <130/80 for 24h ambulatory blood pressure monitoring (24hABPM). | 6 months post intervention |
| Measure | Description | Time Frame |
|---|---|---|
| Adverse events |
| Reported throughout the study period. Approximately 2 years |
| Measure | Description | Time Frame |
|---|---|---|
| Hierarchical analysis testing | Hierarchical analysis testing will be applied to sequential testing of the following hypotheses. Each positive outcome permits the next limb to be tested as a co-primary hypothesis. A negative outcome converts subsequent limbs to secondary hypotheses. [i] Complete biochemical cure for left ablation vs left surgery (positive if non-inferiority (NI) margin <45%) [ii] Complete biochemical cure for all ablation vs all surgery (positive if NI margin <45%) [iii] Complete clinical cure for all ablation vs all surgery (positive if NI margin <33%) The first limb of the hierarchy will be tested if sufficient patients have been recruited on the left, anticipated to be 3 times as many as on the right. |
Inclusion criteria (all of):
Exclusion criteria (any of):
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Aklima Khatun | Contact | 0203 765 8577 | aklima.khatun4@nhs.net | |
| Tumi Kaminsas | Contact | 0207 882 5994 | research.governance@qmul.ac.uk |
| Name | Affiliation | Role |
|---|---|---|
| Morris Brown | Queen Mary University of London | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Cambridge University Hospitals NHS Foundation Trust | Recruiting | Cambridge | SMLG | CB2 0QQ | United Kingdom |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 41887640 | Derived | Laycock K, Kearney J, Lee YN, Macfarlane J, Goodchild E, Ng E, Pineau Mitchell A, Wu X, Htut Z, Goodchild G, Lowe D, Hilliard N, Godfrey E, Qazi N, Bastos J, Chua A, Mahroof R, Palma A, Khatun A, Varsani C, Benu D, Pereira SP, Krishnamurthy M, Cheow H, Chung TT, Carroll P, O'Toole S, Wernig F, Gurnell M, Brown M, Drake WM. Prospective randomised trial comparing thermal ablation With laparoscopic Adrenalectomy as an alternatiVE treatment for unilateral asymmetric primary aldosteronism: a protocol for the WAVE trial. BMJ Open. 2026 Mar 26;16(3):e111798. doi: 10.1136/bmjopen-2025-111798. |
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Clinical trial data may be made available to qualified academic researchers upon approval by the study management committee and completion of appropriate data-sharing and transfer agreements. Data requests must include a clear rationale, the relevance of the proposed research, and a description of the hypothesis, research methodology, statistical analysis plan and intended publication plan.
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PROBE: Prospective Randomised open blinded end point study. Patients are randomized using a minimization program. 2:3 Surgery: Ablation
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PROBE (Prospective, Randomised, Open-label with Blind Endpoint) multi-centre comparison of thermal ablation with laparoscopic adrenalectomy in the treatment of unilateral asymmetric primary aldosteronism.
|
| Unilateral adrenalectomy | Procedure | Unilateral total adrenalectomy for aldosterone producing adenoma. This will be laparoscopic in the vast majority of patients, with open conversion if surgically indicated (unlikely in >1-2 patients) |
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| Anaemia (FBC, requirement for blood transfusion) | Blood test | 6, 12, 24 and 36 months post intervention |
| Renal dysfunction and electrolyte abnormalities (U&Es) | Blood test | 6, 12, 24 and 36 months post intervention |
| Liver dysfunction (LFTs) | Blood test | 6, 12, 24 and 36 months post intervention |
| Pancreatitis (lipase/amylase) | Blood test | 6, 12, 24 and 36 months post intervention |
| Hypertensive urgency (physiological parameters, plasma metanephrines) | Blood test | 6, 12, 24 and 36 months post intervention |
| Length of inpatient stay (hospital episode data) | As reported by patient | 6 weeks post intervention |
| Patient satisfaction (Freiburg index of patient satisfaction) | Completed by patient, using the FIPs score values to rate the treatment they have received. | 6 weeks post intervention |
| Quality of life questionnaire | Completed by patient, using the - EQ-5D 5L and SF-36 questionnaire models to score self rated health and quality of life values. These 2 models are presented as one questionnaire to the patient. | 6 months post intervention |
| Return to usual activities of daily living (self-reported) | As reported by patient | 6 weeks post intervention |
| Anatomical efficacy of ablation | (ablation group only; post-ablation Metomidate/CETO PET-CT appearances) | 6, 12, 24 and 36 months post intervention |
| 6 months post intervention |
| St Bartholomew's Hospital | Recruiting | London | EC1A 7BE | United Kingdom |
|
| University College London Hospital NHS Foundation Trust | Recruiting | London | NW1 2PG | United Kingdom |
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| Guy's and St Thomas' NHS Foundation Trust | Recruiting | London | SE1 9RT | United Kingdom |
|
| Imperial College Healthcare NHS Trust | Recruiting | London | W12 0HS | United Kingdom |
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| Sheffield Teaching Hospitals NHS Foundation Trust | Recruiting | Sheffield | S10 2JF | United Kingdom |
|
| ID | Term |
|---|---|
| D006929 | Hyperaldosteronism |
| ID | Term |
|---|---|
| D000308 | Adrenocortical Hyperfunction |
| D000307 | Adrenal Gland Diseases |
| D004700 | Endocrine System Diseases |
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