Intraoperative temperature measurement during holmium laser enucleation of the prostate – a clinical, experimental trial

Intraoperative temperature measurement during holmium laser enucleation of the prostate – a clinical, experimental trial - TheHoLEP

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00017047

Enrollment

100

Registered

2019-04-05

Start date

2019-04-11

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

N40

Interventions

Group 1: Temperature measurements with patients during holmium-laser-enucleation of the prostate with infra-red-camera, rectal temperature probe and if pre-existing with an folley catheter.

Eligibility

Sex/Gender

Male

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: All male patients (>18yrs) treated with a holmium-laser-enucleation of the prostate in the clinic of urology, department surgery, University medical center, Freiburg im Breisgau.

Exclusion criteria

Exclusion criteria: children <18yrs and female

Design outcomes

Primary

Measure	Time frame
temperature increase - meausrements during the whole surgery. Frequency of measurements at least 1 Hz	—

Secondary

Measure	Time frame
Surgical outcome: Voiding, residual urine, ICIQ (International Consultation on Incontinence Questionnaire), IIEF (International Index of Erectile Function), IPSS (International Prostate Symptom Score) time of outcome meaurements: postoperatively, 3 months, 6 months	—

Countries

Germany

Contacts

Public ContactSimon Hein

Universitätsklinikum Freiburg Department Chirurgie Klilnik für Urologie

simon.hein@uniklinik-freiburg.de0761/270-25820 und 28930

Outcome results

None listed

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