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Robot-assisted Adrenalectomy, Feasibility and Results (ROBADRE)

C

Central Hospital, Nancy, France

Status

Active, not recruiting

Conditions

Adrenalectomy

Study type

Observational

Funder types

Other

Identifiers

NCT07110168
2025PI122

Details and patient eligibility

About

To date, laparoscopy is considered to be the gold standard technique for adrenalectomy. Robotic surgery is beginning to be used, but no series of more than 300 procedures has yet allowed the morbidity, benefits and learning curve of this technique to be assessed. Furthermore, the debate on the benefits of using robotic tools when performing adrenalectomies remains open. At Nancy University Hospital, we have been performing robotic procedures on 90% of our patients since 2009, and have seen a significant increase in patient numbers (currently between 80 and 90 per year).

In 2019, we published a series of 300 patients, describing the results of the technique.

Based on our clinical experience and the growing interest of the surgical community, we believe that describing our cohort of patients who have undergone robot-assisted surgery (estimated at 600 patients) is of unquestionable scientific interest.

In 2018, the American team at UCLA published a series of 640 laparoscopic adrenalectomies and examined the risk factors for complications following this surgery. Given the team's reputation and their publication in the leading surgical journal (JAMA Surgery), we used the same criteria for our data collection to make our results comparable.

This study aims to evaluate the risk factors for surgical complications after robotic adrenalectomy in a large retrospective series. Our aim is to demonstrate the safety and reliability of this technique and to identify patients at greatest risk of complications. This may encourage the adoption of the technique in other centres.

Full description

Main objective:Evaluation of postoperative morbidity (Clavien-Dindo >2) 30 days after robot-assisted unilateral adrenalectomy

Secondary objective(s):

  • Identify risk factors associated with the occurrence of complications after surgery. (patients characteristics, adrenal disease type)
  • Determine the learning curve of robotic adrenalectomy considering surgical morbidity (Clavien Dindo>2)
  • Determine the learning curve of robotic adrenalectomy considering operative time

Data collection:

PREOPERATIVE

Adrenal disease :

  • Conn's adenoma
  • Pheochromocytoma
  • Cushing's adenoma
  • Non-secreting adenoma
  • Metastases (specify primary site: kidney, lung, skin)
  • Virilising tumour
  • Adrenal cancer (adrenocortical carcinoma)
  • Haematological disorders
  • Other

Patient characteristics:

  • Age
  • BMI
  • ASA score
  • Sex
  • Comorbidity (Charleston score?)
  • History of abdominal surgery/specify the procedure, noting whether it was laparoscopic or laparotomy
  • History of adrenal surgery
  • Genetic disease: NEM, VHL, etc.

Intra-operative data :

  • Preoperative blood pressure
  • Tumour laterality
  • Surgeon
  • Operative time
  • Perioperative complications: bleeding, digestive tract injury, etc. ( using the KAARAFANI classification)
  • Conversion to laparotomy and cause: adhesions, bleeding, digestive tract injury

Post-operative data :

  • Length of hospital stay in days
  • Morbidity: complications within 30 days after surgery according to Clavien-Dindo
  • Mortality

Enrollment

700 estimated patients

Sex

All

Ages

16+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • all patient who underwent unilateral robot-assisted adrenalectomy

Exclusion criteria

  • bilateral adrenalectomy
  • adrenalectomy by laparotomy
  • partial adrenalectomy

Trial design

700 participants in 1 patient group

patients who underwent robot assisted adrenalectomy in University Hospital of Nancy
Description:
All patients who underwent a robotic adrenalectomy (all adrenal disease included) in the Department of Visceral,Metabolic and Oncologic surgery in University Hospital of Nancy between 01.01.2013 and 12.31.2025.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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