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Deep Parasternal Intercostal Plane (DPIP) Block

I

Istinye University

Status

Not yet enrolling

Conditions

Postoperative Pain

Treatments

Procedure: block

Study type

Observational

Funder types

Other

Identifiers

NCT06558123
istinye university block

Details and patient eligibility

About

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.

Enrollment

40 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

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

Trial design

40 participants in 2 patient groups

Control
Description:
single level
Treatment:
Procedure: block
study
Description:
two level
Treatment:
Procedure: block

Trial contacts and locations

1

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Central trial contact

ilke dolgun

Data sourced from clinicaltrials.gov

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