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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02733757
Other study ID # CAAE - 03409512.2.0000.5149
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date May 2013
Est. completion date December 2015

Study information

Verified date August 2020
Source Federal University of Minas Gerais
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Regional anesthesia in orbit can reduce ocular blood flow, increase in intraocular pressure (IOP) or the pharmacological action of local anesthetics. This study was conduced to evaluate the effects of clonidine added to lidocaine in IOP, ocular perfusion pressure (PPO) and ocular pulse amplitude (OPA) in patients undergoing cataract surgery under sub-Tenon's and peribulbar anesthesia.


Description:

In this prospective randomized and double blind clinical study, involving 80 patients with ages from 30 to 86 years old, ASA I and II, both genders. The patients were randomly divided into 4 groups of 20 patients, and then were administered in control sub-Tenon's group 5 mL of 2% lidocaine with 1 mL of 0.9% sodium chloride solution; in sub-Tenon's group clonidine, 5 mL of 2% lidocaine associated with 1 µg/kg of clonidine diluted in 1 mL 0.9% sodium chloride solution. In the peribulbar anesthesia, the control group with 6 mL of 2% lidocaine and 1 mL of 0.9% sodium chloride solution, and peribulbar group clonidine, 6 mL of 2% lidocaine associated with 1 µg/kg of clonidine diluted in 1 mL 0.9% sodium chloride solution. Were evaluated the systemic hemodynamic variables; IOP and OPA measurements according the dynamic contour tonometer (DCT) and calculation of OPP, prior to the blockade (M0), and one (M1), five (5) and ten minutes (M10) after the injection of the anesthetic solutions. Complications related to the sub-Tenon's and peribulbar anesthesia were recorded.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date December 2015
Est. primary completion date October 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 30 Years to 86 Years
Eligibility Inclusion Criteria:

- Adults between 30 and 86 years old

- Both genders

- Physical status ASA (American Society of Anesthesiologists) I and II

- Cooperative patients undergoing cataract surgery by phacoemulsification

Exclusion Criteria:

- Patients with communication difficulties

- Allergic to any medication protocol

- Chronic therapy with clonidine

- In use of antihypertensive medication

- Diabetes

- Glaucoma

- Previous surgery in the same eye

- Abnormalities in coagulation

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Clonidine
Clonidine 1 µg/kg plus 2% lidocaine

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Federal University of Minas Gerais Federal University of Espirito Santo

References & Publications (3)

Cabral SA, Carraretto AR, Brocco MC, Abreu Baptista JF, Gomez RS. Effect of clonidine added to lidocaine for sub-Tenon's (episcleral) anesthesia in cataract surgery. J Anesth. 2014 Feb;28(1):70-5. — View Citation

Pianka P, Weintraub-Padova H, Lazar M, Geyer O. Effect of sub-Tenon's and peribulbar anesthesia on intraocular pressure and ocular pulse amplitude. J Cataract Refract Surg. 2001 Aug;27(8):1221-6. — View Citation

Watkins R, Beigi B, Yates M, Chang B, Linardos E. Intraocular pressure and pulsatile ocular blood flow after retrobulbar and peribulbar anaesthesia. Br J Ophthalmol. 2001 Jul;85(7):796-8. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Intraocular Pressure (IOP) Within 10 minutes before the surgery procedure
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