Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
analgesic effect of superficial cervical plexus block by using ultrasound in patients undergoing neck surgeries
The efficacy of ultrasound-guided bilateral superficial cervical plexus block on postoperative pain relief in patients undergoing neck surgeries, prospective randomized controlled study,To assess the analgesic efficacy of bilateral superficial cervical plexus block in reducing post-operative pain following neck surgery, decrease total opoid consumption during first 24h post operative.
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Group will take the block | Active Comparator |
| |
| Controlled group | Placebo Comparator |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| superficial cervical plexus block guided by ultrasound with bupivacaine | Procedure | in active group we will use bupivacaine in superficial cervical plexus block to deal with pain postoperative neck surgeries |
| Measure | Description | Time Frame |
|---|---|---|
| Analgesic effect of bilateral superficial cervical plexus block in postoperative neck surgeries | To assess the analgesic efficacy of bilateral superficial cervical plexus block on postoperative pain following neck surgery, as measured by the Visual Analog Scale Pain was assessed using the Visual Analog Scale (VAS; 0 = no pain, 10 = worst imaginable pain) at 1, 4, 8, 12, and 24 hours postoperatively. | within the first 24 hours postoperatively |
| Measure | Description | Time Frame |
|---|---|---|
| Total opioid consumption | To assess the total opioid consumption within the first 24 hours postoperatively and the time to first analgesic request. | within the first 24 hours postoperatively |
| Measure | Description | Time Frame |
|---|---|---|
| Nausea and vomiting | incidence of postoperative nausea and vomiting | 24 hours postoperative |
| patients satisfaction score | To assess patient satisfaction with postoperative pain management using a 5-point Likert scale (1 = very dissatisfied, 5 = very satisfied). |
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Faculty of medicine, Sohag University. | Sohag | Egypt |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| ID | Term |
|---|---|
| D010149 | Pain, Postoperative |
| ID | Term |
|---|---|
| D011183 | Postoperative Complications |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D010146 | Pain |
Not provided
Not provided
| ID | Term |
|---|---|
| D002045 | Bupivacaine |
| D000082 | Acetaminophen |
| ID | Term |
|---|---|
| D000813 | Anilides |
| D000577 | Amides |
| D009930 | Organic Chemicals |
| D000814 | Aniline Compounds |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Paracetamol (500 mg) tablets | Drug | controlled group will take shame block with normal saline and paracetamol only |
|
| at 24 hours postoperatively |
| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |
| D000588 |
| Amines |
| D000083 | Acetanilides |