Trials / Completed
CompletedNCT03713762
Peribulbar Block: Lidocaine-bupivacaine vs Lidocaine-bupivacaine-fentanyl
Anesthesia With Peribulbar Block: Lidocaine-bupivacaine vs Lidocaine-bupivacaine-fentanyl
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 70 (actual)
- Sponsor
- Centro Medico Docente la Trinidad · Academic / Other
- Sex
- All
- Age
- 45 Years – 90 Years
- Healthy volunteers
- Accepted
Summary
Ophthalmological procedures such as cataract extraction can be carried out with a peribulbar block (PBB). The advantages of this anesthetic technique include a lower incidence of coughing, unwanted movements and emesis during awakening, in addition to providing adequate postoperative analgesia. The researchers want to investigate whether the use of fentanyl citrate by peribulbar route, when administered with a local anesthetic, shortens the anesthetic latency, interfere with the degree of akinesia and if provides greater postoperative analgesia.
Detailed description
Article Type. Clinical trial study
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | peribulbar block 1 lidocaine/bupivacaine | Peribulbar block: 100 mg of lidocaine 5% and 15 mg of bupivacaine 0.5% for a total volume of the anesthetic mixture of 5 ml. |
| DRUG | peribulbar block 2 lidocaine/bupivacaine/fentanyl | Peribulbar block: 100 mg of lidocaine 5%, 15 mg of 0.5% bupivacaine and 50 mcg of fentanyl citrate for a total volume of the anesthetic mixture of 6 ml. |
Timeline
- Start date
- 2009-10-01
- Primary completion
- 2009-11-30
- Completion
- 2009-11-30
- First posted
- 2018-10-22
- Last updated
- 2018-10-23
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT03713762. Inclusion in this directory is not an endorsement.