MedTrace Logo

Evaluation of Duration of Anesthesia and Patient Satisfaction After Retrobulbar Block Applied in Cataract Surgery

NCT04178200 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 80

Last updated 2019-11-26

No results posted yet for this study

Summary

It is aimed to determine patient satisfaction (pain assessment during and after the operation) and the initial and total anesthesia durations of eye lid and globe anesthesia after administration of local anesthetic solution only in standard applied volumes (1.5-3 ml). No agents will be added to the local anesthetic agents used in the conventional retrobulbar block in patients who will undergo cataract surgery,

Conditions

  • Cataract Surgery
  • Patient Satisfaction
  • Akinesia
  • Anesthesia, Local
  • Anesthesia; Adverse Effect
  • Anesthesia Recovery Period

Interventions

DRUG

Lidocaine 2% Injectable Solution 0.75 ml

0.75 ml of Lidocaine will be added to the anesthetic solution.

DRUG

Bupivacaine Hcl 0.5% Inj 0.75 ml

0.75 ml of Bupivacaine will be added to the anesthetic solution.

DRUG

Lidocaine 2% Injectable Solution 1.5 ml

1.5 ml of Lidocaine will be added to the anesthetic solution.

DRUG

Bupivacaine Hcl 0.5% Inj 1.5 ml

1.5 ml of Bupivacaine will be added to the anesthetic solution.

Sponsors & Collaborators

  • Develi Devlet Hastanesi

    lead OTHER_GOV

Principal Investigators

  • Gamze ALBAYRAK, MD · Develi Devlet Hastanesi

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-12-16
Primary Completion
2020-04-24
Completion
2020-04-24

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04178200 on ClinicalTrials.gov