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Role of interfacial plane block for upper abdominal surgery in pediatric population.

Comparison of ultrasoundâ??guided erector spinae plane block vs modified thoracoabdominal nerve block through perichondrial approach for perioperative analgesia in paediatric patients undergoing upper abdominal surgery: a randomized controlled trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/03/050617
Enrollment
40
Registered
2023-03-13
Start date
Unknown
Completion date
Unknown
Last updated
2023-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Erector spinae plane (ESP) block: ESP block will be performed lateral position at the level of T7 transverse process. Under the aseptic precautions a high frequency (6-13MHz) linear pro

Sponsors

AIIMS Patna
Lead Sponsor
AIIMS Patna
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: ASA I and II patients scheduled for upper abdominal surgeries through unilateral upper quadrant incision

Exclusion criteria

Exclusion criteria: 1. Parents refusal to participate in the study 2. Patients with coagulation disorders 3. Patients hypersensitive to study medications 4. Patients with developmental or mental delay 5. Skin lesions or infection at the planned site of needle insertion 6. Subcostal incision extended to opposite side. 7. Patient develop complication (surgical/Anaesthesia) or re-exploration within 24 hours will be excluded from analysis.

Design outcomes

Primary

MeasureTime frame
Intraoperative fentanyl consumptionTimepoint: Total fentanyl consumption during intaoperative period.

Secondary

MeasureTime frame
1. Postoperative pain score using CHEOPS (Childrenâ??s Hospital of Eastern Ontario Pain Scale) 2. To estimate postoperative paracetamol consumption 3. To determine time to first rescue analgesic administration 4. Side effect likes nausea, vomiting and sedation and local anesthetic toxicity Timepoint: pain score at 1, 4, 8, 16, 24 hours at rest.

Countries

India

Contacts

Public ContactAmarjeet Kumar

AIIMS, Patna

amarjeetdmch@gmail.com9570890646

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026