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Serratus Plane Block and Pectointercostal Block - Trial NCT06381765

Access comprehensive clinical trial information for NCT06381765 through Pure Global AI's free database. This phase not specified trial is sponsored by Cukurova University and is currently Recruiting. The study focuses on Postoperative Pain. Target enrollment is 60 participants.

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NCT06381765
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procedure
Trial Details
ClinicalTrials.gov โ€ข NCT06381765
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Serratus Plane Block and Pectointercostal Block
Comparison of Deep Serratus Plane Block With Deep Serratus Plane Block+Pectointercostal Plane Block

Study Focus

Postoperative Pain

ultrasound guided Serratus plane bock and pectointercostal block

Interventional

procedure

Sponsor & Location

Cukurova University

Adana, Turkey

Timeline & Enrollment

N/A

May 10, 2024

Aug 10, 2024

60 participants

Primary Outcome

postoperative morphine consumption,postoperative visual analog scale scores

Summary

ASA I-II female patients aged over 18 who will undergoing breast reduction surgery will
 recruit to the study. Patients will divide into 2 groups. Deep serratus plane block will
 perform with 0,25 %bupivacaine 20 ml at the midaxillary 5. rib, bilaterally for Group I. At
 Group II, deep serratus plane block ( 0,25 %bupivacaine 20 ml) at the midaxillary 5.th rib+
 pectointercostal plane block (0,25% bupivacaine 15 ml) at 4-5.th intercostal space will
 perform bilaterally . General anesthesia with sevoflurane and remifentanil will perform to
 the all patients. Postoperative pain scores, morphine consumption and complications will
 record till the 24.th hours.

ICD-10 Classifications

Acute pain
Postoperative intestinal obstruction
Pain, unspecified
During surgical operation
During surgical operation

Data Source

ClinicalTrials.gov

NCT06381765

Non-Device Trial