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The aim of this study was to compare the efficacy of caudal block and sacral espb used as a postoperative analgesia method in urogenital pediatric surgery cases.
The parents of the patients who will undergo urogenital surgery will be included in the study after being informed and written consent is obtained. They will be randomised and divided into two groups. After general anaesthesia, sacral espb will be performed in the 1st group and caudal block will be performed in the 2nd group and postoperative pain will be evaluated with Face, Leg, Activity, Cry, Consolability (FLACC) score.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| SESPB | Experimental | Participants received ultrasound-guided SESPB before the surgery |
|
| CAUDAL | Active Comparator | Participants received ultrasound-guided caudal block before the surgery |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Ultrasound-guided sacral erector spinae plane block | Procedure | Patients were received ultrasound-guided sacral erector spinae plane block, 1ml/kg %0.25 bupivacaine (max 20 ml), for postoperative pain management |
| Measure | Description | Time Frame |
|---|---|---|
| Face, Leg, Activity, Cry, Consolability (FLACC) score | The FLACC is an observational pain scale. It is widely used in the paediatric population to assess pain in infants and children who are unable to verbally express their pain.Each category is scored on the 0-2 scale which results in a total score of 0-10. | baseline ,and 24 hours |
| Measure | Description | Time Frame |
|---|---|---|
| Analgesic requirement | If the FLACC>4 and above rescue analgesics will be made | baseline, and 24 hours |
| Satisfaction of the patient's parents | A questionnaire will be used in which patient's parents will indicate their satisfaction from 0 to 10. 0: not at all satisfied, 10: very satisfied |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Bilge Olgun KeleÅŸ | Giresun University | Principal Investigator |
| Dilek Yeniay | Giresun University | Study Chair |
| Elvan Tekir Yılmaz | Giresun University | Study Chair |
| İlke Tamdoğan | Giresun University | Study Chair |
| Mehmet DeÄŸermenci | Giresun University | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Giresun Research and Training Hospital | Giresun | Central | 28100 | Turkey (Türkiye) |
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Randomized controlled double blind study
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Randomisation using a closed envelope method based on computer-generated random numbers was to assign patients to two equal groups. Group 1 received midline US-guided sacral erector spinae plane block and Group 2 received caudal block. The experienced anesthetist who opened the envelope performed the block according to the group code and patients were followed postoperatively by an anesthetist blinded to which block was performed. Patients were also blinded as to which block was performed.
| Ultrasound-guided caudal block | Procedure | Patients were received ultrasound-guided caudal block, 1ml/kg %0.25 bupivacaine (max 20 ml), for postoperative pain management |
|
| 24. hours |
| Satisfaction of the surgeons | A questionnaire will be used in which surgeon's will indicate their satisfaction from 0 to 10. 0: not at all satisfied, 10: very satisfied | 24.hours |
| ID | Term |
|---|---|
| D000091642 | Urogenital Diseases |
| D010149 | Pain, Postoperative |
| ID | Term |
|---|---|
| D011183 | Postoperative Complications |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D010146 | Pain |
| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |
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