Feasibility and safety profile of posterior retroperitoneoscopic adrenalectomy in high-risk patients

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00018793

Enrollment

100

Registered

2019-10-11

Start date

2019-02-01

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

E27

Interventions

Group 1: Retrospective data analysis of patients with a high-risk profile with regard to perioperative complications on the basis of a retrospective database. Group 2: Compared to the high-risk group

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Retroperitoneoscopic adrenalectomy in hospital Reinbek from 2014 to 2018

Exclusion criteria

Exclusion criteria: No retroperitoneoscopic adrenalectomy in hospital Reinbek

Design outcomes

Primary

Measure	Time frame
The primary endpoint is postoperative complications within 90 days of surgery.	—

Secondary

Measure	Time frame
As a secondary endpoint, the size of the removed adrenal gland was evaluated in the histopathological examination immediately postoperatively.	—

Countries

Germany

Contacts

Public ContactJonas Herzberg

Krankenhaus Reinbek St. Adolf-Stift

jonas.herzberg@krankenhaus-reinbek.de00494072805375

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026