Deep Parasternal Intercostal Plane (DPIP) Block

Completed

• Conditions: Postoperative Pain
• Interventions: Procedure: block

• Registration Number: NCT06558123
• Lead Sponsor: Istinye University

Brief Summary

In this study, we aimed to compare the effects of this block, which is routinely applied in our hospital but has not been studied in our hospital or in the literature before, on the pain in the first 24 hours after the operation, between the single-level and the two-level block.

Detailed Description

Not available

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study First Submitted: 2024-08-14
• Study First Submitted QC: 2024-08-14
• Study Start: 2024-08-15
• Study First Posted: 2024-08-16
• Status Verified: 2024-12
• Primary Completion: 2024-12-15
• Study Completion: 2024-12-20
• Last Update Submitted: 2024-12-24
• Last Update Posted: 2024-12-27

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

• Adult patients aged 18 years and older
• American Society of Anesthesiologists physical status of II-III
• Undergoing elective coronary artery bypass grafting (CABG), valve repair/replacement, or combined CABG/valve procedure via median sternotomy

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Exclusion Criteria

• Patients who are unable to communicate
• Patients who have had emergency surgery, reoperation, thoracotomy or mastectomy
• Patients with a history of chronic pain
• Patients who are using chronic opioids or sedatives
• Patients who have had a re-sternotomy within 24 hours of surgery
• Patients with liver or kidney failure
• Patients who are using narcotics

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Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Control	block	single level
study	block	two level

Primary Outcome Measures

Name	Time	Method
numeric rating scale	4 month	24 hours pain

Trial Locations

Locations (1)

Istinye Üniversity; 🇹🇷 Istanbul, Merkez Mahallesi, Turkey