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Comparison of Anterior Chamber Paracentesis and Conventional Mannitol Infusion in Patients With Primary Acute Angle-closure Glaucoma

T

Taipei Medical University

Status

Completed

Conditions

Glaucoma
Acute Primary Angle-closure Glaucoma

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The investigators wanted to reported the results of immediate anterior chamber paracentesis (ACP), compared to Mannitol infusion, in patients with acute primary angle-closure glaucoma (PACG). In this study, the investigators first divided patients into three sub-groups according to their initial intraocular pressure (IOP) for analyzing the differences of IOP control, severity of corneal edema, waiting time for laser peripheral iridotomy (LPI), and visual outcome between ACP and Mannitol infusion.

Full description

The investigators demonstrated that ACP could be first considered in patients with initial IOP between 45 to 60 mmHg because it provided better visual outcome than Mannitol infusion through the rapid stabilization of the anterior segment, which was achieved by rapid IOP control, better corneal edema regression, shortening waiting time for LPI. However, ACP should be considered in patients with the initial IOP of 60mmHg and higher only when Mannitol was contraindicated.

Enrollment

60 patients

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • first attack of acute PACG;
  • initial presenting IOP was higher than 45 mmHg;
  • diagnosis confirmed by gonioscopic examination;
  • patients within 48 hours of symptom onset.

Exclusion criteria

  • been incompletely followed up within 2 weeks;
  • been using anti-glaucomatous medication before ACP or Mannitol infusion;
  • previous intraocular surgeries on the same eye;
  • contraindication for Mannitol;
  • history of other vision-threatening ocular diseases.

Trial design

60 participants in 2 patient groups

Experimental Group
Control Group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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