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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04153123
Other study ID # CAAE 04433113.0.0000.5149
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 1, 2013
Est. completion date May 31, 2014

Study information

Verified date November 2019
Source Federal University of Minas Gerais
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Evaluate ophthalmic artery flow by echo-Doppler before and after peribulbar block with lidocaine in presence or absence of epinephrine.


Description:

There are controversies regarding the ophthalmic artery (OA) flow after peribulbar block with the addition of epinephrine. Therefore, we aimed to evaluate OA flow by echo-Doppler before and after peribulbar block with lidocaine in presence or absence of epinephrine.

Fifty-six patients that were eligible for cataract phacoemulsification surgery were selected. Patients were divided into two groups: group 1 - Peribulbar block with lidocaine and 1/200.000 epinephrine; group 2 - Peribulbar block with lidocaine in the absence of epinephrine. The resistance index (RI) of OA was evaluated using echo-Doppler before and 10 min after the peribulbar block.


Recruitment information / eligibility

Status Completed
Enrollment 26
Est. completion date May 31, 2014
Est. primary completion date May 31, 2014
Accepts healthy volunteers No
Gender All
Age group 30 Years to 85 Years
Eligibility Inclusion Criteria:

- American Society of Anesthesiologists (ASA) I, II or III physical status classification

- Cataract surgery

Exclusion Criteria:

- glaucoma

- diabetic retinopathy

- previous eye surgery in the same eye

- ocular trauma

- allergic to any protocol medication

- uncooperative patients or cognitive difficulties

- axial eye diameter of less than 21.0 mm or greater than 25.5 mm.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Epinephrine


Locations

Country Name City State
Brazil Universidade Federal de Minas Gerais, Faculdade de Medicina, Departamento de Cirurgia. Belo Horizonte Minas Gerais

Sponsors (1)

Lead Sponsor Collaborator
Federal University of Minas Gerais

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Artery resistance index of ophthalmic artery The resistance index (RI) of OA was evaluated using echo-Doppler before and 10 minutes after the peribulbar block. Change on resistance index 10 minutes after peribulbar anesthesia
See also
  Status Clinical Trial Phase
Completed NCT04036201 - Minimum Effective Volume of Local Anesthetic for Peribulbar Block.Does it Differ With the Eyeball Axial Length? N/A