Clinical Trials Directory

Trials / Completed

CompletedNCT05706285

Comparing Intrathecal Morphine With Erector Spina Plane Block in Open Gastrectomy Surgery

Comparing Postoperative Analgesic Effects of Intrathecal Morphine With Erector Spina Plane Block in Open Gastrectomy Surgery

Status
Completed
Phase
Study type
Observational
Enrollment
63 (actual)
Sponsor
Marmara University · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

Summary

Open gastrectomy causes severe postoperative pain due to wide surgical incisions, retraction of the abdominal wall and direct manipulation of the visceral organs. It leads to delayed postoperative recovery, increased medical expenses and poor surgical outcomes. Epidural analgesia, intrathecal morphine and patient-controlled analgesia are frequently used in the postoperative pain management of abdominal surgeries. Intrathecal morphine is applied as a standard protocol in many centers due to its ease of application and effective pain control. However; it has undesirable effects such as postoperative nausea-vomiting, itching and most importantly respiratory depression. Regional interfascial plane blocks, such as erector spina plane block, have recently been popular in clinical practice to provide postoperative pain control. Erector spina plane block, when placed preoperatively, is expected to reduce opioid consumption and improve outcomes. The primary implication of this study is to compare postoperative pain scores and opioid consumption. It is also aimed to compare the effectiveness of Numeric Rating Scale and Clinically Aligned Pain Assessment Tool used in postoperative pain assesment.

Conditions

Interventions

TypeNameDescription
PROCEDURERegional Block ComparisonComparing postoperative pain and opioid consumption in groups

Timeline

Start date
2023-02-15
Primary completion
2024-02-01
Completion
2024-02-01
First posted
2023-01-31
Last updated
2024-03-28

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT05706285. Inclusion in this directory is not an endorsement.