Paraumbilical Hernia Clinical Trial
Official title:
Comparison Between External Oblique Intercostal Plane Block and the Transversus Abdominis Plane Block in Paraumbilical Hernia Repair as Analgesia for Intraoperative and Postoperative Pain.
AIM OF STUDY: Comparison between effect of external oblique intercostal plane block and the Oblique subcostal transversus abdominis plane block in paraumbilical hernia repair as analgesia for intraoperative and postoperative pain.
Status | Not yet recruiting |
Enrollment | 62 |
Est. completion date | December 29, 2026 |
Est. primary completion date | October 28, 2026 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility | Inclusion Criteria: 1. Age between 18 and 65 years with a body mass index (BMI) of 18-35 kg/m2 2. patients with the American Society of Anesthesiologists (ASA) physical status I/II 3. Patients scheduled for elective paraumbilical hernia Exclusion Criteria: - 1-Known hypersensitivity to the study drugs. 2-Body Mass Index > 40 kg/m2. 3- Inability to accurately describe postoperative pain to investigators. 4-Opioid tolerance or dependence. 5-Preexisting history of chronic pain. 6-History of renal, liver, cardiac, neuropsychiatric disorder problems. 7-Bleeding or coagulation abnormality. 8-Patients who received any analgesic 24 h before surgery 9-Patients who have difficulty understanding the study protocol |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Assiut University |
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* Note: There are 17 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The effect between external oblique intercostal plane block and the transversus abdominis plane block in paraumbilical hernia repair as analgesia for intraoperative and postoperative pain according to numeric rating score (NRS) | numeric rating scale : from 0 to 10 0 : no pain
1 - 3 : mild pain 4 - 6 : moderate pain 7 - 9 : severe pain 10 : worst pain possible |
baseline | |
Secondary | time of the first opioid request | time of the first opioid request all over 24 hours postoperatively. | baseline | |
Secondary | Heart rate | heart rate will be recorded at time 0 then every 15 minutes in the first 2 hours, then at 6, 12, 24 hours postoperatively. | baseline | |
Secondary | Mean arterial blood pressure | mean arterial blood pressure will be recorded at time 0 then every 15 minutes in the first 2 hours, then at 6, 12, 24 hours postoperatively. | baseline | |
Secondary | time to start ambulation | time of the patient first movement will be recorded | baseline |
Status | Clinical Trial | Phase | |
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Completed |
NCT03766061 -
Onlay Mesh Hernioplasty Vs Sublay Mesh Hernioplasty for Paraumbilical Hernia Repair
|
N/A |