Trials / Completed
CompletedNCT05609565
Intrathecal Prilocaine and Adductor Canal Block vs Intrathecal Bupivacaine Alone for Ambulatory Knee Arthroscopy
Hybrid Anesthesia for Ambulatory Knee Arthroscopy Using Intrathecal Prilocaine and Adductor Canal Block vs Intrathecal Bupivacaine Alone: a Randomized Controlled Trial
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 80 (actual)
- Sponsor
- Ain Shams University · Academic / Other
- Sex
- All
- Age
- 21 Years – 60 Years
- Healthy volunteers
- Not accepted
Summary
\- Although bupivacaine is safe and has a low rate of transient neurologic symptoms, the prolonged sensory and motor block is a drawback for day-case spinal anesthesia.Intrathecal hyperbaric prilocaine causes a much shorter motor block, with a similar onset time and lower inter-individual variability in motor block duration. Furthermore, the peripheral nerve block is used as an adjunct to the spinal anesthesia to prolong the surgical anesthetic conditions.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | spinal anesthesia with hyperbaric prilocaine+adductor canal block (ACB) with bupivacaine | spinal anesthesia with hyperbaric prilocaine+adductor canal block (ACB) with bupivacaine |
| DRUG | spinal anesthesia with bupivacaine | spinal anesthesia with bupivacaine |
Timeline
- Start date
- 2022-11-15
- Primary completion
- 2024-09-30
- Completion
- 2024-09-30
- First posted
- 2022-11-08
- Last updated
- 2024-11-26
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT05609565. Inclusion in this directory is not an endorsement.