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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04294394
Other study ID # 2019/514/150/22
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 1, 2020
Est. completion date January 15, 2021

Study information

Verified date January 2021
Source Kocaeli Derince Education and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Effective analgesia is very important in terms of preventing respiratory, thromboembolic complications and providing early mobilization after open thoracotomy. Although thoracic epidural analgesia is gold standart method for this aim, it causes common side effects such as hypotension, dural puncture,motor block In recent years, with the effective use of ultrasonography, different regional anesthesia methods have been developed to prevent such complications


Description:

A total of 75 patients will be included in the study in three groups: group ESPB, group RIB and control group (group K). Under general anesthesia, patients who will undergo both ESPB and RIB will be applied block with a 22 G and 100 mm block needle, accompanied by ultrasonography, and 20 ml 0.25% bupivacaine. Apart from the standard peroperative analgesia protocol applied to all three groups, no additional procedure will be performed in group control. Postoperative analgesic consumption amount, first analgesic requirement time and visual analog scale (VAS) values of the patients will be recorded.


Recruitment information / eligibility

Status Completed
Enrollment 75
Est. completion date January 15, 2021
Est. primary completion date January 5, 2021
Accepts healthy volunteers
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - Patients between 18-75 years old - ASA1,2,3 group patients - Patients undergoing thoracotomy under general anesthesia Exclusion Criteria: - The patient's refusal to participate in the study - Allergy to local anesthetics

Study Design


Related Conditions & MeSH terms


Intervention

Other:
rhomboid block
Rhombid block, on the other hand, is a method which make up analgesia by providing lokal anestethetic enjection between intercostal muscles and rhomboid muscles and blocks between t3- t9 levels
erector spinae block
The Erector spinae plan block is a recently developed regional block method .Adminestering of lokal anesthetic between the transver proces and erector spinae muscles provides the dorsal and ventral branch blokades of regional spinal nerve and make up the analgesia.It have a wide range usage such as surgery of thoracal and abdominal area
control
For postoperative analgesia, all patients (including Rhomboid block and Erector spinae block) will be administered 100 mg tramadol and 1 gr paracetamol. No additional intervention other than this medical approach will be applied in the control group.

Locations

Country Name City State
Turkey Tahsin Simsek I?stanbul
Turkey Derince Egitim Ve Arastirma Hastanesi Kocaeli Derince

Sponsors (1)

Lead Sponsor Collaborator
Kocaeli Derince Education and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary rhomboid block versus erector spinae block in thorachotomy In this study, we aimed to compare the effects of rhomboid block and erector spinae block in pain control after thoracotomy the study will comlete in three month
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