Deep Parasternal Intercostal Plane (DPIP) Block

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

40 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-08-15

Study Completion Date

2024-12-20

Brief Summary

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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.

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Detailed Description

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Conditions

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Postoperative Pain

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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Control

single level

block

Intervention Type PROCEDURE

Single Level and Two Level Deep Parasternal Intercostal Plane (DPIP) Block

study

two level

block

Intervention Type PROCEDURE

Single Level and Two Level Deep Parasternal Intercostal Plane (DPIP) Block

Interventions

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block

Single Level and Two Level Deep Parasternal Intercostal Plane (DPIP) Block

Intervention Type PROCEDURE

Eligibility Criteria

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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

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

Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No