Trials / Enrolling By Invitation
Enrolling By InvitationNCT06910696
Erector Spinae Plane Block Versus Modified Thoracolumbar Interfascial Plane Block
Erector Spinae Plane Block Versus Modified Thoracolumbar Interfascial Plane Block for Rapid Recovery and Rehabilitation After Lumber Discectomy: A Randomized Study
- Status
- Enrolling By Invitation
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 144 (estimated)
- Sponsor
- Zagazig University · Other Government
- Sex
- All
- Age
- 21 Years – 64 Years
- Healthy volunteers
- Not accepted
Summary
the purpose of this study is to compare of better postoperative analgesia following lumber spine discectomy
Conditions
- Achievement of High-quality Analgesia, Rapid Recovery With Rehabilitation in Lumber Spine Discectomy
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Regional Anesthetic Injection | The probe will be placed in the parasagittal plane at the level of the L3 vertebrae. The spinous process will be visualized, and the probe was moved 3 cm laterally from the midline. The erector spinae musclewill be visualized above the transverse process. The needle will be punctured in the craniocaudal direction using the in-plane technique. The needle will be directed superior to the transverse process . Then, 2 mL normal saline solution will be injected into the deep fascia of the erector spinae muscle to confirm the proper injection site. After ensuring the location of the needle, 20 mL of 0.25% bupivacaine will be administered. The same ESPB procedure will be performed on the other side. In total, 40 mL of 0.25% bupivacaine was administered |
| DRUG | Regional Anesthetic Injection | The probe will be placed vertically at the L3 vertebrae level. The spinous process and the interspinous muscles (i.e., multifidus, longissimus, and iliocostalis) will be visualized as the anatomic guide points. The probewill be moved laterally to identify the longissimus and iliocostalis muscles . The needlewill be inserted between the longissimus and iliocostalis in the medial-to-lateral direction using the in-plane technique. After confirming the location of the needle, 20 mL of 0.25% bupivacaine will be administered. The same mTLIP procedure will be performed on the opposite side. In total, 40 mL of 0.25% bupivacaine will be administered |
Timeline
- Start date
- 2025-04-11
- Primary completion
- 2025-09-01
- Completion
- 2025-12-01
- First posted
- 2025-04-04
- Last updated
- 2025-04-15
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT06910696. Inclusion in this directory is not an endorsement.