percutanous volume reduction to the intervertebral disc trough Nukleoplasty

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00004958

Enrollment

150

Registered

2013-05-28

Start date

2013-01-01

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

M51

Interventions

Group 1: The patients receive pre-/ postoperative a questionnaire including questions towards the functional status (oswestry disability index), pain in different body- regions and patients descriptiv

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: non- sequestred lumbar intervertebral disc prolaps

Exclusion criteria

Exclusion criteria: Tumor, local or systemic infection

Design outcomes

Primary

Measure	Time frame
functional outcome, measures through a patient- based questionnaire, providing the oswestry disability index of the patient, filled out preoperativ and postoperativ after 2 days/ 14 days/ 2 month/ 6 month/ 1 year and 2 years.	—

Secondary

Measure	Time frame
complication rate perioperative, assessed through the data provided by the surgeon and the doctoral reference until the direct dismisson of the patient from the hospital	—

Countries

Germany

Contacts

Public ContactBastian Himpe

UKSH, Sektion für Orthopädie

bastian.himpe@uksh.de004915782451116

Outcome results

None listed

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