NCT03972852Completed
Establishment of an Anaesthetic Protocol for Examinations for Children With Glaucoma or Suspected Glaucoma
Establishment of an Anaesthetic Protocol for Examinations Under Anaesthesia for Children With Glaucoma or Suspected Glaucoma - Correlation of Bispectral Index (BIS) and Intraocular Pressure (IOP)
Source: ClinicalTrials.gov · Last updated 2 Jan 2026
Brief summary (registry, in English)
Correct measurement of the intraocular pressure of children with glaucoma or suspected glaucoma is essential for diagnosis and therapy. Despite new non-invasive measurement methods most of the children are uncooperative during the ophthalmological examination. Therefore examination under anaesthesia is needed. A lot of perioperative factors influence the measurement of intraocular pressure. Established and safe anaesthetic regimes have been modified regarding these factors. Aim of the study is to evaluate, if a standardized anaesthetic protocol generates reliable and reproducible measured values.
- Status (registry)
- Completed
- Study type
- Observational
- Enrollment
- 120 (actual)
- First submitted
- 31 May 2019
- Start date
- Jun 2019
- Primary completion date
- May 2022
- Lead sponsor
- Johannes Gutenberg University Mainz
- Diseases
- Glaucoma
- NCT number
- NCT03972852
What you commit to
- Study type: Observational
- Participants enrolled: 120
- From Jun 2019 to the primary completion date, May 2022
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Known allergy to propofol or remifentanil
Other
- Contraindication for a laryngeal mask airway
Who the study is looking for
- Indication for a general anesthesia (laryngeal mask) and ophthalmological examination and probably surgery
- Children with glaucoma or suspected glaucoma
- ASA classification I-III
- written informed consent of the legal representatives
Age in the registry: 5 months to 10 years · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Johannes Gutenberg-Universität Coordinator of this site? Confirm its status | Mainz | Germany | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.