Study on the functional testing of glaucoma surgical procedures using non-invasive stress tests

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00038910

Enrollment

460

Registered

2026-01-07

Start date

2024-09-01

Completion date

Unknown

Last updated

2026-01-12

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

Conditions

H40

Interventions

Group 1: Patients requiring glaucoma surgery to regulate intraocular pressure. The examinations are planned to be performed preoperatively and postoperatively at 6 and/or 12 weeks, as well as at 6 an

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Individuals with a confirmed diagnosis of glaucoma who are scheduled for surgical treatment. The prerequisite is that the patients are capable of giving informed consent and agree to the procedure.

Exclusion criteria

Exclusion criteria: - Missing informed consent form - Allergy to local anesthetic

Design outcomes

Primary

Measure	Time frame
Intraocular pressure reduction during stress test	—

Secondary

Measure	Time frame
- Intraocular pressure reduction - Number of pressure-lowering medications used - Implant location (categorized) - Incision size - Incision position (categorized)	—

Countries

Germany

Contacts

Public ContactAnna-Karina Maier-Wenzel

Charité

anna-karina.maier@charite.de+4930450654419

Outcome results

None listed

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