N/A
Completed N=75
Comparison Between Ultra Sound Guided Rectus Sheath Block and Field Block for Midline Hernia Repair
Ultrasound Guided Rectus Sheath Block · Pain, Postoperative
Source: ClinicalTrials.gov NCT03225313 ↗
Enrolled (actual)
75
Serious AEs
0.0%
Results posted
Jul 2019
Primary outcomePrimary: Immediate Postoperative Pain — 7.36; 1.04; 6.56 score on a scale
Summary
Randomized double blinded controlled clinical trial will be done with a total number of 75 patients will be divided into 3 groups. To compare between Ultra-sound guided rectus sheath block VS Field block infiltration in providing a good analgesia for patients undergoing midline hernia repair to detect which one is superior.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Immediate Postoperative Pain |
7.36; 1.04; 6.56 | — |
| PRIMARY Postoperative Pain at 2 Hours After Procedure. |
6.04; 1.20; 5.12 | — |
| PRIMARY Postoperative Pain at 6 Hours After Procedure. |
5.28; 2.64; 5.16 | — |
| SECONDARY Change in the Level of Serum Cortisol. |
307.84; 214.00; 286.92 | — |
| SECONDARY Measurement of Serum Adrenaline Levels (ng/ml) Using ELISA Technique. |
2.508; 2.556; 2.704 | — |
| SECONDARY Measurement of Serum Noradrenaline Levels (ng/ml) Using ELISA Technique. |
9.960; 20.880; 12.932 | — |
| SECONDARY Measurement of Serum Cortisol Level (Nmol/ Liter) Using ELISA Technique. |
159.02; 327.05; 170.52 | — |
| SECONDARY Measurement of Serum Adrenaline Level (ng/ml) Using ELISA Technique. |
1.42; 3.96; 2.00 | — |
Eligibility Criteria
Inclusion Criteria
- Elective midline hernia repair surgery.
- Age: adult patients between 18 - 60 years old.
- Gender: Both male and female.
- ASA Class: I & II.
Exclusion Criteria
- Refusal of patient.
- Pregnancy and lactation.
- Fever or sepsis.
- Patients ASA III or IV.
- Addicts and drug abusers.
- Patients taking corticosteroids or any cardio - active drugs.
- Local infection at site of the injection.
- Allergy to any of the study medications.
Data sourced from ClinicalTrials.gov (NCT03225313). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.