Erector Spinae Plane (ESP) Block For Postoperative Pain Management In Lumbar Spine Surgery : A Randomized Control Trial
| Registry | NCT03997227 |
|---|---|
| Status | Unknown |
| Phase | Not applicable |
| Study type | Interventional; randomized, parallel, masking: single, treatment |
| Enrollment | 68 (Estimated) |
| Sponsor | Aydin Adnan Menderes University (Other) |
| Conditions | Erector Spinae Block |
| Interventions | Erector spinae Block (Procedure) |
| Dates | start 2019-05-02, primary completion 2020-05-02 (estimated), completion 2020-07-02 (estimated), first posted 2019-06-25, last updated 2019-06-27 |
| Locations | 1 site in Turkey (Türkiye) |
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Lumbar vertebra surgery is one of the most common surgical procedures. After lumbar veretebra surgery, patients complain of excessive pain. Postoperative pain usually occurs in the early postoperative period and delays patient mobilization and thus lengthens hospital stay.
The aim of this study was to investigate the effect of this field block on postoperative pain and respiratory function in patients undergoing ESP with lomber vertebra surgery and with ultrasound guidance for postoperative analgesia.
Lumbar vertebra surgery is one of the most common surgical procedures. After lumbar veretebra surgery, patients complain of excessive pain. Postoperative pain usually occurs in the early postoperative period and delays patient mobilization and thus lengthens hospital stay.
The aim of this study was to investigate the effect of this field block on postoperative pain and respiratory function in patients undergoing ESP with lomber vertebra surgery and with ultrasound guidance for postoperative analgesia.
ASA I-III, 68 patients between 18-75 years of age were planned to be included in the study. 34 participants were expected to be included in the control and implementation group.
In our study, the ESP block was planned to be applied to the patients in the block group. Peroperative analgesia plan will be applied to all patients in the same way. In this protocol, intravenous paracetamol 1 gr and tramadol 1 mg / kg were determined. Then, every eight hours, paracetamol and contromal infusion.
At the end of the operation, the patients will be determined by the Numeric Rating Scale (NRS) system at the 30th hour, 1st, 6th, 12th and 24th hours after the first hour of the operation. Tramadol PCA and paracetamol are administered every eight hours.
Age, sex, weight, body mass index, application of ESP block, time of surgery, duration of surgery, evaluation of pain in postoperative recovery room and 24-hour follow-up will be recorded when the patient is mobilized and discharged.
It is thought that the ESP block will decrease postoperative pain by providing effective pain control after surgery in patients undergoing lumbar vertebra surgery. In addition, it is thought to accelerate mobilization in the postoperative period and shorten the time of discharge.
| Arm | Type | Interventions | Description |
|---|---|---|---|
| Block group | Active comparator | Procedure: Erector spinae Block | |
| control group | No intervention |
Sex: All, ages: 18 Years to 75 Years
Inclusion Criteria: * 68 patients * ASA I-III, * Aged 18-75 years * underwent lumbar spine surgery under elective conditions Exclusion Criteria: * Presence of contraindications to LA agents used in this study * Use of chronic opioids, * Psychiatric disorders. * Surgical procedures that lasted <60 minutes or> 300 minutes * The presence of infection at the injection area.
| Facility | City | Country | Status |
|---|---|---|---|
| Adnan Menderes Univesity | Aydin | Turkey (Türkiye) | Recruiting |