Ultrasound Guided Paravertebral Block Versus Erector Spinae Block for Postoperative Analgesia After Inguinal Hernia Repair in Pediatric Patients

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age24-12
SponsorZagazig University

About this trial

The aim of the study is to compare postoperative analgesia in pediatric patients undergoing inguinal hernia repair by comparing the efficacy of ultrasound guided paravertebral block versus ultrasound guided erector spinae plane block.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • ultrasound guided paravertebral block

    Procedure/Surgery

    after sterilization and identifying the level of T10 ,linear ultrasound probe will be placed in the midline over the spinous process at the chosen level, then the probe will be moved laterally to view the lamina and hyperechoic transverse process ,the pleural should be visible as a bright white line .The needle should be inserted in -plane from lateral to medial and the needle tip should end in a hypoechoic triangular space. Correct needle placement should be confirmed by anterior displacement of pleura with injection of small volume of saline then 0.5 ml/kg of a mixture of 0.25 ℅ bupivacaine and 1℅ lidocaine (1:1) will be injected

  • Ultrasound guided erector spinae plane block

    Procedure/Surgery

    After sterilization, the linear ultrasound probe will be placed over transverse process of T10 ,after optimizing the image in sagittal or transverse scanning ,A 50 mm 22-G needle will be placed under the erector spinae muscle in -in plane orientation until it contacted T8 transverse process in the cranial caudal direction ,after hydro dissection and confirmation that the tip of the needle is between the transverse process and the fascia of the erector spinae muscle group, 0.5 ml/kg of a mixture of 0.25 ℅bupivacaine and 1℅ lidocaine (1:1) will be injected

  • control group C

    Procedure/Surgery

    will receive standard general anesthesia with pain management protocol without regional block.

Treatment groups

158 Participants
are divided into 3 treatment groups
Group A: Group paravertebral (PVB) blockActive comparator 1 intervention
Group B: Group erector spinae plane (ESP) blockActive comparator 1 intervention
Group C: Control group (group C)Active comparator 1 intervention

Trial outcomes

Primary outcomes

1

The total amount of rescue analgesia (Ibuprofen consumption)

The total consumption of rescue analgesia (Ibuprofen consumption) postoperative

Time frame
for 24 hours postoperative

Secondary outcomes

1

Pain intensity at rest (static) and after movement or coughing (dynamic)

by using 10 points Modified Objective Pain Score (MOPS)(0=no pain, 1-3=mild pain, 4-6=moderate pain, and 7-10= sever pain)

Time frame
0 minutes immediate postoperative ( on arrival to PACU), 30 minutes, 1hs, 2hs, 4hs, 8hs, 12 hrs and 24hs postoperatively
2

The time to first request of rescue analgesia (Ibuprofen)

the time from giving block till time of first request of ibuprofen when MOPS \> 3 at rest or after movement

Time frame
for 24 hours postoperative
3

The total number of patients requiring additional dose of intraoperative fentanyl.

Number of patients receive additional dose of intra operative fentanyl ( increase in the mean blood pressure or heart rate 20% above base line readings, fentanyl in a dose 0.5 mcg/kg will be given to the patient)

Time frame
during operation period
4

To record the incidence of complications

To record the incidence of complications (hematoma, local anesthetic toxicity, pneumothorax, infection, hypotension, epidural or intrathecal spread)

Time frame
24 hours postoperative

Other outcomes

Locations

2

Map coordinates are unavailable for these locations. Locations are shown below instead.

Faculty of Human Medicine, Zagazig UniversityRecruiting El SharkiaEgyptEgypt
faculty of human medicine, Zagazig university hospitalsRecruiting El SharkiaEgyptEgypt

Sponsors and contacts

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